Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1
Athina Angelopoulou
 -- 19311 2024-02-05 14:35:22 |
2 In accordance to the Encyclopedia Editor suggestions the main part and description were reduced
Athina Angelopoulou
 -13880 word(s) 5431 2024-02-06 14:37:12 | |
3 removed the citation of exra tables and schemes
Peter Tang
 -2 word(s) 5429 2024-02-07 04:43:08 | |
4 format change
Peter Tang
 Meta information modification 5429 2024-02-07 04:44:26 | |
5 Discussion part was removed in accordance to guidelines
Athina Angelopoulou
 -666 word(s) 4763 2024-02-08 11:13:29 | |
6 format change
Peter Tang
 Meta information modification 4763 2024-02-17 03:30:59 |

Video Upload Options

Do you have a full video?
Send video materials Upload full video

Confirm

Are you sure to Delete?
Yes No
Cite
If you have any further questions, please contact Encyclopedia Editorial Office.
Avgoustakis, K.; Angelopoulou, A. Biomaterial-Based Responsive Nanomedicines for Targeting Solid Tumor Microenvironments. Encyclopedia. Available online: https://encyclopedia.pub/entry/54770 (accessed on 03 May 2024).
Avgoustakis K, Angelopoulou A. Biomaterial-Based Responsive Nanomedicines for Targeting Solid Tumor Microenvironments. Encyclopedia. Available at: https://encyclopedia.pub/entry/54770. Accessed May 03, 2024.
Avgoustakis, Konstantinos, Athina Angelopoulou. "Biomaterial-Based Responsive Nanomedicines for Targeting Solid Tumor Microenvironments" Encyclopedia, https://encyclopedia.pub/entry/54770 (accessed May 03, 2024).
Avgoustakis, K., & Angelopoulou, A. (2024, February 05). Biomaterial-Based Responsive Nanomedicines for Targeting Solid Tumor Microenvironments. In Encyclopedia. https://encyclopedia.pub/entry/54770
Avgoustakis, Konstantinos and Athina Angelopoulou. "Biomaterial-Based Responsive Nanomedicines for Targeting Solid Tumor Microenvironments." Encyclopedia. Web. 05 February, 2024.
Biomaterial-Based Responsive Nanomedicines for Targeting Solid Tumor Microenvironments
Edit
This entry is adapted from the peer-reviewed paper 10.3390/pharmaceutics16020179

Solid tumors are composed of a highly complex and heterogenic microenvironment, with increasing metabolic status. This environment plays a crucial role in the clinical therapeutic outcome of conventional treatments and innovative antitumor nanomedicines. Scientists have devoted great efforts to conquering the challenges of the tumor microenvironment (TME), in respect of effective drug accumulation and activity at the tumor site. The main focus is to overcome the obstacles of abnormal vasculature, dense stroma, extracellular matrix, hypoxia, and pH gradient acidosis. In this endeavor, nanomedicines that are targeting distinct features of TME have flourished; these aim to increase site specificity and achieve deep tumor penetration. The development of such systems has significantly advanced the application of biomaterials in combinational therapies and in immunotherapies for improved anticancer effectiveness.

biomaterials tumor microenvironment nanomedicine hypoxia acidosis resistance tumor vasculature targeting stimuli-responsiveness

1. Introduction

Cancer incidence and mortality has increased dramatically, with female breast cancer being the most commonly diagnosed, surpassing lung cancer [1][2]. It represents a major public health issue in emerging and developing countries, and poses great socioeconomic and psychological challenges. According to recent world statistics, cancer is the first or second leading cause of death; there are nearly 20 million new cases and almost 10 million deaths [1]. Global cancer statistics have estimated that near to 30 million new cases should be expected by 2040, and this is expected to affect more developed than emerging economies. Due to migration and demographic changes, the rate of cancer incidence is seriously affected by everyday risk factors, such as tobacco and alcohol use, unhealthy diet, and anxiety [1][2]. Despite the disappointing statistics, however, there was a decline in the overall cancer death rate of about 33% between 1991 and 2020. Furthermore, an estimated 4 million deaths were prevented. Moreover, a decline of 65% in cervical cancer incidence among women in their 20s during the period 2012 to 2019 was observed. This is due to the preventive effect of the human papillomavirus vaccine [1][2]. The decline in rates of cancer mortality can, undoubtedly, be related to increased research efforts in the field of cancer vaccines (RNA technologies) and personalized nanomedicines [3]. The greatest challenges for scientists are to ensure early diagnosis and prevention of cancer, which could effectively reduce cancer mortality.

Early diagnosis is crucial due to the high differentiation rate of tumor cells that promote the development of highly aggressive cancerous cells associated with multidrug resistance (MDR), stemness [4], and invasion [5]. A critical stimulus of MDR and invasion is tumor microenvironment (TME) (Scheme 1). This is a complicated interpenetrating network of varied cancerous and stromal cell types, extracellular matrix (ECM), and interstitial fluid (IF) [6][7][8]. TME is hostile to normal cells while being hospitable to stromal cells that are the nonmalignant components of solid tumors. These include endothelial cells (ECs), fibroblasts (FCs), immune cells (lymphocytes, macrophages, dendritic cells), and perivascular cells (PCs). These cells are interconnected in a protein-rich matrix that promotes angiogenesis and neovascularization [9][10]. Within the heterogenic TME, vasculature abnormalities are related to variations in oxygenation. Furthermore, the elevated presence of reactive oxygen species (ROS), glutathione (GSH), enzymes, and adenosine triphosphate (ATP) further promote a hypoxic status with acidic pH levels (pH 5.5–6.2). These features—in combination with secreted growth factors, cytokines, chemokines, and macromolecules such as proteases and proteins in the surrounding stroma—regulate the stimulation of cancer-associated fibroblasts (CAFs), and play key role in metastatic potency [11][12][13]. The stroma in combination with the highly dynamic ECM act as supportive reservoirs that directly or indirectly interconnect TME with capillary and vascular system cells, and immune system cells. This provide the essential nutrition components of oxygen, gas exchange, and metabolites withdrawal, to support tumorigenesis and continuous neovascularization [14][15][16].

Pharmaceutics 16 00179 sch001
Scheme 1. Schematic representation of solid tumor microenvironment. (Created with the assistance of BioRender.com https://app.biorender.com/user/signin?illustrationId=6156d45891063d00af8af51d (accessed on 1 September 2023 up to 31 November 2023) and Microsoft ppt).

The greatest difficulty posed by the TME of solid tumors is MDR. This results in reduced therapeutic efficiency of traditional interventions such as chemo- and radiotherapy. The backbone of traditional therapeutic approaches is surgical ablation followed by chemo- and radiotherapy or a combination of both, depending on tumor severity. Chemo- and radiotherapy cause serious side effects for the patients within the therapeutic window of the administered doses [17]. Great progress has been achieved with advanced investigation of new therapeutic agents including peptides, antibodies, and prodrugs [18][19][20][21][22]. However, the success of these compounds is compromised by the limitations of abnormal vasculature, heterogenic basement membranes, and poor blood supply. These are all inherited by TME, and are the causes of therapeutic failure [23][24][25]. Nanomedicine represents an important strategy to improve the delivery of therapeutic agents such as drugs, peptides, antibodies, proteins, genes, and immunotherapeutic agents in a selective and controlled manner for efficient accumulation and stimuli responsiveness [26][27][28][29][30][31][32][33][34]. Although great progress has been achieved in this field, the clinical translation of nanomedicines is still limited. In this research, the researchers aim to present a discussion on the field of responsive nanomedicines. This will emphasize the application of biomaterials including natural polymers such as polysaccharides, biodegradable polymers, and metal oxides, in targeting the TME of solid tumors. Biomaterials represent a field of distinct research interest, due to their unique inherent properties. Their structure allows for effective functionalization for the co-delivery of multiple compounds and for effective responsiveness to an internal (chemical and/or biological) or external physical stimulus (magnetic field, light, radiation, ultrasound). Biomaterials have proved to be great supporters of theranostic applications in cancer treatment [35][36]. Overall, in this research the researchers will discuss the role of biomaterial-based nanomedicines in targeting the TME. This includes heterogenic vasculature, tumor stroma ECM, CAFs, tumor hypoxia, and acidosis. The researchers will examine the most recent advances in therapeutic nanomedicine for solid tumors; these have the potential to improve clinical outcomes. Finally, the researchers will summarize the challenges and future outlook for the application of nanomedicines in tumor immunotherapy and combinational therapy to overcome limitations and improve the therapeutic outcome.

2. Solid Tumor Nanomedicine: Distribution in Tumor Microenvironment

Intriguingly, solid tumors are pathological organ-like tissues with heterogenic TME and increased metabolic status, which promote and support processes mimicking normal tissues, as angiogenesis [37][38][39]. Due to the elevated dysregulation of angiogenetic factors, abnormal and destabilized blood and lymphatic vessels are developed. These have major variations in diameter, density, shape (spiral-like) and overall distribution within TME. Additionally, a simultaneous discontinuation of endothelium with leaking cell gaps, irregularly thick or thin basement membranes and disruption of blood flow cause excessive spatial stress and increased interstitial fluid pressure (IFP) [40][41][42]. These features promote the transport of nutrients, oxygen, and blood away from the central region of solid tumors. This stimulates ATP regulation, hypoxia, and acidosis. The same features prohibit the transfer of therapeutic drugs, and this results in an inferior targeting effect and heterogenic tumor distribution of drugs [43]. Nanomedicines improve targeting effectiveness and selectivity [44][45][46]. This is especially the case when they are supported by an enhanced permeability and retention (EPR) effect, which promotes extravasation and effectual intratumor localization [47] (Scheme 2). Despite progress being made, moderate clinical success has been achieved so far. This is because nanomedicine applications have encountered severe obstacles related to avascular tumor sites due to the TME’s characteristics restricting nanomedicines’ access only to highly vascular regions with increased perfusion [47][48]. These limitations in the therapeutic efficacy of nanomedicines have been tackled recently by exploiting the complex mechanisms and associated properties of TME. This improves intratumoral localization. Furthermore, specially designed nanomedicines exhibit stimuli-responsiveness in TME features, such as hypoxia and acidity, by combining ligand-mediated active targeting of selective receptors with growth factors, inhibitors, enzymes, and peptides. Combining the benefits of external stimuli-responsiveness has, beneficially, increased the targeting efficiency of nanomedicines and amplified the therapeutic activity [49][50][51][52].

Nanomedicines that target solid tumors traverse a highly variable environment. This emphasizes the importance of adaptability and spatiotemporal pharmacological activity. The current treatment strategies that aim to overcome MDR and the multi-factorial TME rely on a combination of chemo-, radio-, and immunotherapies (Scheme 3). Approved nanomedicines are co-administered for improved synergistic therapeutic effect. In this way, biomaterials have greatly assisted in orchestrating the pharmacokinetics and targeting potential of nanomedicines. This is due to their inherent properties of biodegradability and ease of surface modification which offer effective sites for receptor-mediated ligand targeting (peptides, antibodies, nucleic acids, small organic molecules). Biomaterials also make possible theranostic applications of nanomedicines for real-time therapy and monitoring of tumor tissues. Moreover, biomaterials can be appropriately functionalized to obtain stimuli-responsiveness and manipulate TME hypoxia and spatial pH distribution (acidic extracellularly vs. basic intracellularly). In addition, the effectual combination of biomaterials with acquired responsiveness on varied external stimuli (hyperthermia, photodynamic, sonodynamic) has highly improved tumor-specific accumulation. This modulates cellular apoptotic cascades and promotes cellular death by associated gene regulation [53][54][55]. In this respect, biomaterials are important for TME-responsive applications, and they demonstrate promising results in combinational therapies and immunotherapies. Some of these are FDA-approved or under clinical trials for specific tumor types (Table 1) [56][57][58][59]. The clinical trials and applications of nanomedicines have mostly relied on improving drugs’ activity, as well as reducing side effects, and on enhancing biodistribution of drugs and agents within solid tumor tissues. For this, strategies have been developed to overcome physical, biological, and chemical obstacles in the TME, and achieve efficient specificity on molecular targets (such as cellular receptors, CAFs, CSC) and physiological factors (such as ECM, angiogenesis, IFP) [50][55][60]. The innate biological properties of biomaterials against opsonization have offered great support, because they provide longer and efficient systemic circulation time of the nanomedicines [61]. Natural polymers and synthetic biodegradable polymers which have been extensively reviewed and discussed for their application in the pharmaceutical and biomedical fields include: (i) polysaccharides such as alginic acid (alginate), dextran, agarose, hyaluronic acid, carrageenan, chitosan, and cyclodextrin: (ii) protein-based polymers such as gelatin, albumin, soy, and collagen; and (iii) synthetic polymers such as polyesters, polyamides, polyanhydrides, phosphorous based, and polyurethanes [62][63][64][65][66][67]. In solid tumor therapeutics, the benefits of novel theranostic and multifunctional nanomedicines are a niche research area that aims to overcome the limitations of TME and design novel therapies [67] (Scheme 1). In the following, the researchers discuss novel therapeutic and targeting concepts of biomaterial-based nanomedicines which exploit TME specificity and responsiveness.
Pharmaceutics 16 00179 sch002
Scheme 2. Representation of nanomedicine accumulation and targeting, through the EPR effect and site-specific TME targeting. (Created with the assistance of BioRender.com https://app.biorender.com/user/signin?illustrationId=6156d45891063d00af8af51d (accessed on 1 September 2023 up to 31 November 2023), and Microsoft ppt).

Table 1. Therapeutic nanomedicines approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA).

Carrier Type

Product Name

Therapeutic Agent

Cancer Type

Stage

Ref.

Liposomes

Zolsketil®

Doxorubicin

Metastatic breast cancer, advanced ovarian cancer, multiple myeloma, AIDS-related Kaposi’s sarcoma

(https://www.ema.europa.eu/en/medicines/human/EPAR/zolsketil-pegylated-liposomal (accessed on 15 January 2024)

Approved (EMA, 2022)

[56][57]

Vyxeos®

Cytarabine:

daunorubicin

Newly diagnosed therapy-related acute myeloid leukemia, acute myeloid leukemia with myelodysplasia related changes

(https://www.ema.europa.eu/en/medicines/human/EPAR/vyxeos-liposomal-previously-known-vyxeos, accessed on 15 January 2024)

Approved (EMA, 2018) (FDA, 2017)

[56][57]

Onivyde®/CPX-351

Irinotecan

Pancreatic cancer

(https://www.ema.europa.eu/en/medicines/human/EPAR/onivyde-pegylated-liposomal-previously-known-onivyde, accessed on 15 January 2024)

Approved (EMA, 2016) (FDA, 2015)

 [56][57]

Mepact®

Mifamurtide

Osteosarcoma

(https://www.ema.europa.eu/en/medicines/human/EPAR/mepact, accessed on 15 January 2024)

Approved (EMA, 2009)

[56][57]

Ameluz®

5-aminolevulinic acid

Superficial and/or nodular basal cell carcinoma

(https://www.ema.europa.eu/en/medicines/human/EPAR/ameluz, accessed on 15 January 2024)

Approved (EMA, 2011)

[56][57]

DaunoXome®

Daunorubicin

Kaposi’s sarcoma

Approved (FDA 1996)

Discontinued

(FDA, 2021)

[56][57]

Iron Oxide nanoparticles

NanoTherm®

Fe2O3

Glioblastoma, prostate, and pancreatic cancer

(https://www.eib.org/en/stories/new-cancer-treatments, accessed on 15 January 2024)

Approved (EMA, 2013)

[57]

Albumin nanoparticles

Abraxane®

Paclitaxel

Metastatic breast cancer, locally advanced or metastatic non-small cell lung cancer, metastatic

adenocarcinoma of the pancreas

(https://www.ema.europa.eu/en/medicines/human/EPAR/abraxane, accessed on 15 January 2024)

Approved

(EMA 2008)

(FDA 2005)

[57][58]

Pazenir®

Paclitaxel

Metastatic breast cancer, metastatic adenocarcinoma of the pancreas, non-small cell lung cancer

(https://www.ema.europa.eu/en/medicines/human/EPAR/pazenir, accessed on 15 January 2024)

Approved (EMA 2019)

[58]

Vaccines

Adstiladrin®

Adenoviral vector-based gene therapy

Bacillus Calmette–Guérin unresponsive non-muscle invasive bladder cancer with carcinoma in situ with or without papillary tumors

(https://www.fda.gov/drugs/resources-information-approved-drugs/fda-disco-burst-edition-fda-approval-adstiladrin-nadofaragene-firadenovec-vncg-patients-high-risk, accessed on 15 January 2024)

Approved (FDA 2022)

[59]

Provenge®

Autologous peripheral-blood mononuclear cells

Metastatic castration-resistant prostate cancer (mCRPC)

(https://www.drugs.com/history/provenge.html, accessed on 15 January 2024)

Approved (EMA 2013) (FDA 2010)

Discontinued

(EMA, 2015)

[59]
Pharmaceutics 16 00179 sch003
Scheme 3. Scheme showing various opportunities provided by nanomedicines for effective TME targeting of solid tumors. Nanomedicines can focus on targeting axes of (i) heterogenic vasculature, (ii) stroma extracellular matrix (ECM), (iii) stroma cancer-associated fibroblasts (CAFs), (iv) hypoxia, and (v) acidosis. Here are presented various nanomedicines evaluated for these targeting axes, e.g., liposomes, human serum albumin (HSA) particles, hydroxyapatite (HA) particles, chitosan (CS) and its derivatives, chitosan-lipid nanoparticles, peptide self-assembling particles, polymeric particles (PLA, PLGA, and pegylated PLA and PLGA), and mesoporous silica nanoparticles (MSN). The therapeutic processes take advantage of growth factors (VEGF, PDGF, CTGF), membrane-bonded proteins such as MMPs, and HIF-1 and pH gradients. They are investigated in single or in combination therapies with anticancer drugs, redox-GSH/ROS sensitivity, photodynamic therapy (PDT), hyperthermia, and ultrasounds. The combination of targeting ability with TME responsiveness may result in more efficient solid tumor therapeutics by exploitation of the innate features of biomaterials. (Created with the assistance of BioRender.com https://app.biorender.com/user/signin?illustrationId=6156d45891063d00af8af51d (accessed on 1 September 2023 up to 31 November 2023), and Microsoft ppt).

3. Nanomedicines for Targeting TME: Application of Natural and Synthetic Biomaterials

3.1. The Heterogenic Vasculature

Angiogenetic mechanism is divided into two phases: the avascular, wherein tumor progression is suppressed due to controlled homeostasis of pro- and anti-angiogenetic factors; and the vascular, wherein tumor development is promoted by a switched homeostasis favoring a pro-angiogenetic environment. For solid tumors, in order to progress and develop, a de facto ultimate need is presented for blood, oxygen, and nutrient supply. This is supported by the continuously evolving tumor vasculature (Scheme 4) [68][69][70]. Thus, regulating angiogenesis is a key step in tackling TME abnormal vasculature that is being targeted by nanomedicines through angiogenetic inhibitors. The intention is to promote tumor suppression mechanisms by limiting the unrestricted vascular development [71]. The main target of angiogenetic therapeutics is the inhibition of growth factors of the pro-angiogenetic domain that present elevated affinity with surface receptors of ECs. These include: (i) soluble factors such as vascular endothelial growth factor (VEGF family factors comprising A to F members), platelet-derived growth factor (PDGF), beta and alpha transforming growth factors (TGF-α, -β), angiopoietins (Ang); and (ii) insoluble membrane-bound proteins such as ephrins, integrins, cadherins, matrix metalloproteinases (MMPs), and hypoxia-inducible factor-1 (HIF-1) (Scheme 5) [72].
Pharmaceutics 16 00179 sch004
Scheme 4. Presentation of the heterogenic vasculature of TME, where (1) pro-angiogenetic activities of ECs including junction destabilization, migration, proliferation, and vessel branching result in unrestricted vascular development (2). Characteristics of the abnormal vasculature are the disrupted, leaky blood vessels (3) and increased interstitial fluid pressure (black arrows). (Created with the assistance of BioRender.com https://app.biorender.com/user/signin?illustrationId=6156d45891063d00af8af51d (accessed on 1 September 2023 up to 31 November 2023), and Microsoft ppt).

3.2. The Tumor Stroma Extracellular Matrix

Therapeutic approaches against solid tumors expand on targeting tumor stroma (Scheme 6). This is a dynamic heterogenic matrix that commonly comprises cellular components such as cancer-associated fibroblasts (CAFs), mesenchymal stromal cells, innate and adaptive immune cells, macrophages, and non-cellular compartments such as extracellular matrix (ECM), tumor vasculature, and interstitial matrix [73][74]. Tumor stroma has been recognized as a critical part of TME because its abundant components can support the transformation of normal cells to tumorous cells, promoting tumorigenesis and progression [75]. In this process, ECM plays a pivotal role in the development and support of homeostasis of tumor tissue. ECM is mainly composed of proteins (such as collagen, fibrilin, and elastin), proteoglycans, and polysaccharides (hyaluronic acid or hyaluronan). The unrestrained cross-linking of hyaluronic acid with collagen type I results in a densely rigid network. This represents a critical obstacle for host immune systems’ function [76]. Tumor ECM has dynamic features and a pronounced effect on supporting TME vascularization [77]. It also (i) presents a physical barrier for drug perfusion; (ii) induces cell adhesion-mediated drug resistance owing to the elevated presence of ECM proteins; (iii) activates glycolysis and glutamine metabolism to provide an abundant energy supply for tumor cells; (iv) promotes aggressiveness and metastasis by the deposition of malignant cells to the tumor endothelium [76][77][78]. Various factors participate in ECM maintenance, including growth factors (VEGF, PDGF, Ang, stromal cell derived factor, SCDF) and proteins (MMP family). These factors are the target of ECM-specific nanomedicines [79].
Pharmaceutics 16 00179 sch006
Scheme 5. Effective targeting of TME extracellular matrix (ECM). The tumor stroma ECM is a dynamic rigid construction of proteins such as collagen and elastin, and proteoglycans and polysaccharides such as hyaluronan. Nanomedicine targeting ECM are based on (1) the promotion of degradation processes against ECM by the use of hyaluronidase and degradation enzymes, (2) the application of biomimic peptides to modulate biosynthesis of ECM by promoting artificial ECM or inhibiting connective tissue growth factors, and (3) the combination of ECM degradation with drug-delivery vehicles. Biomaterials such as PLGA-PEG nanoparticles, liposomes, antibodies, superparamagnetic iron oxide nanoparticles, and peptide nanoparticles have been evaluated for these applications. (Created with the assistance of BioRender.com https://app.biorender.com/user/signin?illustrationId=6156d45891063d00af8af51d (accessed on 1 September 2023 up to 31 November 2023), and Microsoft ppt).

3.3. The Tumor Stroma Cancer Associated Fibroblasts

Tumor stroma is a dynamic environment that orchestrates tumor progression, angiogenesis, invasion, and metastasis through various components, including stromal cells such as cancer-associated fibroblasts (CAFs), mesenchymal stem cells (MSCs), ECs, stellate cells, and adipocytes (Scheme 7). CAFs are activated fibroblasts that, in contrast to normal fibroblasts, have established a prevailing role in (i) the increased rate of proliferation and migration, (ii) the ability to regulate tumorigenesis, (iii) the development of inter- and intracellular interactions with tumor cells, (iv) metabolic reprogramming of tumor cells during tumor initiation, (v) energy supply through oxidative phosphorylation for sustaining the elevated proliferation rate, and (vi) autophagy and oxidative stress pathways [80]. CAFs targeting is a strategically crucial therapeutic field of TME-intervening nanomedicines. This is because CAFs are related to drug resistance by secreting proteins, cytokines, and extracellular vehicles that protect malignant tumor cells and make TME hostile to antitumor agents and host immune attack [81][82][83]. The essential role of CAFs in tumorigenesis, multidrug resistance (MDR), and metastasis has been addressed in this research by responsive biomaterials applied on the targeting of cellular surface markers for CAFs depletion, and on the normalization of activated CAFs for phenotype reprogramming. Among surface biomarkers, the most distinguishing and well-researched are fibroblast activation protein-α (FAP-α), which represents a poor prognostic marker [84]; and α-smooth muscle actin (α-SMA), which has been identified as a novel biomarker [85]. FAP is a transmembrane glycoprotein (antigen) that is present in almost 90% of stromal fibroblasts, and its effective targeting and suppression induced CD8+ T cell-mediated damage of CAFs. This results in inhibition of tumor growth [83][84][86].
Pharmaceutics 16 00179 sch007
Scheme 6. Effective targeting of cancer-associated fibroblasts (CAFs) in TME by nanomedicines based on biomaterials. Two distinct approaches are presented in this research: the depletion of CAFs though (A) antibody delivery, FAP and α-SMA inhibitors delivery; (B) vaccine delivery and promotion of CD8+ T cells; and (C) CAR T cells with FAP specificity that inhibit FAP+ CAFs activity via CD8+ T cells upregulation. (Created with the assistance of BioRender.com https://app.biorender.com/user/signin?illustrationId=6156d45891063d00af8af51d (accessed on 1 September 2023 up to 31 November 2023), and Microsoft ppt).

3.4. The Tumor Hypoxia

Another therapeutic target of responsive nanomedicine is the TME hypoxia. This is a direct consequence of heterogenic vasculature and fluctuating blood flow, and results in insufficient oxygen diffusion and perfusion within the tumor environment. The rapid proliferation rate of tumor and stromal cells creates excessive consumption of supplied oxygen, nutrients, and energy [87]. Imbalance in the diffusion mechanisms of oxygen supply is observed at depths after 70–150 μm from peripheral tumor blood vessels. This results in gas oxygen (gas-O2) levels falling below 1–2% in hypoxic solid tumors. There are two types of hypoxia: the chronic, wherein oxygen’s concentration is characterized by a longitudinal gradient drop for a prolonged time period of several hours; and the acute, in which tumor ECs and stromal cells are attached to vasculature with deprived oxygen perfusion [88]. Extensive research has resulted in the understanding of hypoxia mechanisms and their effects on tumor biology by participating in the regulation of angiogenesis, metastasis, and multidrug resistance [89][90]. Hypoxia-regulated genes are expressed among various tumor types with high hypoxic gene expressions such as the squamous cell carcinoma (SCC) of the head and neck, lung, and cervix tumors; these have also been investigated [91].

Scheme 7. Tumor hypoxia represents a significant target for responsive nanomedicines. Important axes of nanomedicine research are GLUT targeting, multidrug resistance targeting, increase of chemo-sensitivity, M1/M2 macrophage polarization, increase of tumor oxygenation, and antioxidants. Biomaterials used for hypoxia targeting nanomedicines include polysaccharides, polymers, hybrid nanoparticles, metal oxides and hybrid metal–polymer nanoparticles, polymersomes, nanogels, and liposomes in combination with chemotherapeutic drug targeting (CDT), magnetic targeting, and PDT/PTT therapy. (Created with the assistance of BioRender.com https://app.biorender.com/user/signin?illustrationId=6156d45891063d00af8af51d (accessed on 1 September 2023 up to 31 November 2023), and Microsoft ppt).

3.5. The Tumor Acidosis

Tumor and stromal cells use aerobic glycolysis for their amplified energy supply requirements, as a direct consequence of hypoxia and defective vasculature. Aerobic glycolysis is an oxygen-independent process known as the Warburg effect. However, even in normally oxygenated tumor regions, the main energy supplier remains aerobic glycolysis in about 80% of solid tumors [92]. In aerobic glycolysis, glucose constitutes the main macronutrient of tumor cells for their biosynthetic requirements and follows the lactate metabolic pathway, through GLUT transporters producing amplified levels of lactic acid (lactate). The main transcriptional factors of glycolytic activity regulating lactate production are the HIF-1α and c-Myc regulatory genes [93] that promote the overexpression of varied glycolytic enzymes such as lactate dehydrogenase A (LDHA), and monocarboxylate transporters (MCTs) such as MCT1 and MCT4 [94]. Mainly, the upregulation of LDHA gene favors the activity of LDH-5 and inhibits the activity of LDH-1, and promotes the conversion of pyruvate to lactate. Through this metabolic pathway, elevated amounts of lactate, protons (H+), and carbon dioxide (CO2) are secreted into TME. This leads to acidosis [95]. Acidosis regulates the metabolism of innate and adaptive immune cells by: (i) hindering the function of CD8+ T, natural killer (NK), natural killer T (NKT) and dendritic (DC) cells; (ii) supporting regulation of FOXP3+ T cells (Treg); and (iii) promoting M2 activated macrophage polarization. Overall, the acidic TME is an immunosuppressive incubator of pro-oncogenic and tumorigenic factors, and has been extensively studied for targeted nanomedicine applications [96][97][98]. The glycolytic metabolic pathway and acidic pH gradient are key participating factors in MDR due to their activation of enzymes and proteins responsible for resistance, efflux of drugs through P-gp, and stimulation of migration [99][100].
In tumors, a unique pH-gradient effect is established, with extracellular pH levels (pHe) being more acidic (6.4–7.0) and intracellular pH (pHi) being more alkaline (7.25–7.50). Distinct pH variations exist in tumor cell organelles, and they can be divided into acidic, such as nucleosomes and lysosomes with a pH of 5.5 and 5.0, respectively; or alkaline, such as mitochondria and cytoplasm, which have a corresponding pH of 8.0 and 7.2, respectively. The pH gradient is associated with the expression of membrane transporters such as MCT1, MCT4, carbonic anhydrases, and sodium-bicarbonate co-transporter (NBC). These participate in the translocation of lactic acid, CO2, and its bicarbonate ion byproducts. Other mechanisms influencing TME acidity are the efflux of endosomes acidic cargo and the release of the acidic intracellular comportments of necrotic cells. In stimuli responsive nanomedicine, pH sensitivity has been highly exploited and reviewed [101][102][103][104][105]. Apart from drug delivery systems, tumor acidosis was targeted by pH-regulating molecular systems at various stages of clinical trials (this is described by Corbet et al.) [106], and by TME sensitive platforms for combined endogenous stimuli responsive effects (as reviewed by Wang et al. [107]).

3.6. Tumor Immunotherapies

Another important area of nanomedicine research is tumor immunotherapy. Tumor immunotherapies may represent a vital solution in TME limitation and can be divided into immune checkpoint inhibitors (ICI), immune tumor vaccines, and chimeric antigen receptor-modified CAR T cells. The development of nanomedicines for cancer immunotherapy is largely based on the application of biomaterials such as polysaccharides (e.g., hyaluronic acid, alginic acid, chitosan, and dextran) and synthetic polymers including PEG, PLA, PLGA, PCL, and polypeptides [108]. The development of immunotherapeutic nanomedicines based on biomaterials has emerged as a strategy to improve therapeutic outcome by inducing tissue-specific immunomodulation through cell, antibody, and gene immune responses [109]. Opportunities to apply biomaterials in tumor immunotherapy and their combination with conventional therapies have been interestingly reviewed [110][111][112]. Among immunotherapies, immune checkpoint inhibitors present promising therapies that mainly target cytotoxic T lymphocyte-associated molecule-4 (CTLA-4), programmed cell death receptor-1 (PD-1), and programmed cell death receptor-1 ligand (PD-L1). Immune checkpoints are proteins on the surface of immune T cells that recognize and bind to partner proteins on tumor cells, and promote intracellular inhibitory signals and immunosuppressive enzymes; this suppresses host immune T cell attack against tumor cells. Hu et al. [113] developed amphiphilic nanoparticles with a core from hydrophobic ROS-sensitive poly(thioketal phosphoester) and a shell from hydrophilic lecithin/DSPE-PEG, encapsulating doxorubicin, Ce6 photosensitizer, and anti-PD-L1 antibody for ICI. The nanoparticles were evaluated in 4T1 tumor-bearing mice. Rapid degradation of the ROS-responsive core triggered DOX release and, in combination with laser irradiation, promoted effective PDT activity due to the Ce6 component of the nanoparticles. The combinational effect with the anti-PD-L1 antibody ICI promoted the maturation of DCs, and this significantly suppressed the growth of primary tumors and effectively inhibited distant tumor growth. Another type of immunotherapy is the delivery of immunostimulatory agents that directly activate immune T cells by binding of agonistic antibodies on surface receptors such as CD40, OX40 (CD134), and CD137; this promotes downstream signaling pathways for T cell-mediated antitumor activity [114][115][116][117].
The application of biomaterials in cancer vaccines has made significant progress due to the advantageous effect on enhancing the safety profile and stimulating antigen-specific T cell response. Immunotherapy vaccines aim to activate the immune system attack against tumor cells by downregulating the immune tolerance to tumor antigens, through the combined delivery of immunostimulatory agents to activate host immune cells and immunogenic epitopes of specific tumor antigens [114][115]. Τhe effective delivery of the immunotherapy vaccines to dendritic cells is crucial, because DCs are the main antigen presenting immune cells. Rosalia et al. [115], reported that PLGA nanoparticles coated with agonistic aCD40-mAb and encapsulating tumor associated Ag protein successfully primed CD8+ T cells; thus, the survival of tumor-bearing mice was prolonged. In another study, Wang et al. [116] investigated amphiphilic pH-sensitive galactosyl dextran-retinal (GDR) nanogels with a pH-sensitive hydrazone bond for dextran conjugation with all-trans retinal (a metabolite of vitamin A). The nanogels were galactosylated to acquire DC-targeting ability and were effective vaccine delivery systems due to their ability to successfully amplify major histocompatibility class I, MHC I, antigen expression in DCs, and induced effective antitumor immune responses.
The most recent immunotherapies are CAR T cell and CAR T cell receptor therapies. CAR T cells are engineered immune cells originating from the peripheral blood mononuclear cells of the patient’s blood that are harvested and stimulated to become T cells with specific DNA encoding to recognize certain tumor antigens. There are two FDA-approved CAR T cell therapies for blood cancer; however, their application in solid tumors remains challenging. Nevertheless, CAR T cell therapies against solid tumors are being studied ongoing clinical trials [114][115]. Biomaterials are promising candidates for CAR T cell modification improving the therapeutic efficacy and immune-editing processes [117]. Moreover, nano-biomaterials can improve the effect of immunotherapies, and trigger enhanced therapeutic outcomes and regulation of immune cells by overcoming the barriers of the cold tumor immune microenvironment [118].

4. Conclusions

Responsive biomaterials are broadly researched for the development of nanomedicines that target the TME of solid tumors; they have attracted considerable interest in both fundamental research studies and clinical applications. Natural and synthetic biomaterials are essentially investigated in varied nanomedicine due to their ability of functionalization in order to obtain internal and external stimuli responsiveness and to carry therapeutic and diagnostic agents. Their TME-targeting applications have spread in nanomedicines used for the heterogenic vasculature, tumor stroma extracellular matrix and CAFs, hypoxia, and acidosis. Nanomedicines based on biomaterials have great prospects in terms of immune reprogramming and cancer vaccines for novel therapeutic approaches. The effect of responsive biomaterials in combinational therapy is significant, and this has triggered intense research interest in the evaluation of signaling pathways and mechanisms associated with multidrug resistance and immunosuppression. Moreover, the extensive development of nanomedicines over the past two decades promoted immunotherapies that focus on triggering the patients’ immune system ability to recognize and attack cancer cells. In this research, the theory of targeting nanomedicines that are based on biomaterials is presented for the treatment of solid tumors through specific responses in the dense and heterogeneous tumor microenvironment.

References

  1. Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249.
  2. Siegel, R.L.; Miller, K.D.; Wagle, N.S.; Jemal, A. Cancer statistics 2023. CA Cancer J. Clin. 2023, 73, 17–48.
  3. World Health Organization. World Health Statistics 2022: Monitoring Health for the SDGs, Sustainable Development Goals; World Health Organization: Geneva, Switzerland, 2022; p. 23.
  4. Peng, S.; Xiao, F.; Chen, M.; Gao, H. Tumor-Microenvironment-Responsive Nanomedicine for Enhanced Cancer Immunotherapy. Adv. Sci. 2022, 9, 2103836.
  5. Miao, L.; Lin, C.M.; Huang, L. Stromal barriers and strategies for the delivery of nanomedicine to desmoplastic tumors. J. Control. Release 2015, 219, 192–204.
  6. Liu, J.; Chen, Q.; Feng, L.; Liu, Z. Nanomedicine for tumor microenvironment modulation and cancer treatment enhancement. Nano Today 2018, 21, 55–73.
  7. Yang, S.; Gao, H. Nanoparticles for modulating tumor microenvironment to improve drug delivery and tumor therapy. Pharmacol. Res. 2017, 126, 97–108.
  8. Das, M.; Law, S. Role of tumor microenvironment in cancer stem cell chemoresistance and recurrence. Int. J. Biochem. Cell Biol. 2018, 103, 115–124.
  9. Ribeiro Franco, P.I.; Perillo Rodrigues, A.; Borges de Menezes, L.; Pacheco Miguel, M. Tumor microenvironment components: Allies of cancer progression. Pathol. Res. Pract. 2020, 216, 152729.
  10. Wei, R.; Liu, S.; Zhang, S.; Min, L.; Zhu, S. Cellular and Extracellular Components in Tumor Microenvironment and Their Application in Early Diagnosis of Cancers. Anal. Cell. Pathol. 2020, 2020, 6283796.
  11. Gagliardi, A.; Giuliano, E.; Venkateswararao, E.; Fresta, M.; Bulotta, S.; Awasthi, V.; Cosco, D. Biodegradable Polymeric Nanoparticles for Drug Delivery to Solid Tumors. Front. Pharmacol. 2021, 12, 601626.
  12. Martin, J.D.; Miyazaki, T.; Cabral, H. Remodeling tumor microenvironment with nanomedicines. WIREs Nanomed. Nanobiotechnol. 2021, 13, 1730.
  13. Saini, H.; Eliato, K.R.; Veldhuizen, J.; Zare, A.; Allam, M.; Silva, C.; Kratz, A.; Truong, D.; Mouneimne, G.; LaBaer, J.; et al. The role of tumor-stroma interactions on desmoplasia and tumorigenicity within a microengineered 3D platform. Biomaterials 2020, 247, 119975.
  14. Klemm, F.; Joyce, J.A. Microenvironmental regulation of therapeutic response in cancer. Trends Cell Biol. 2015, 25, 198–213.
  15. Deasy, S.K.; Erez, N. A glitch in the matrix: Organ-specific matrisomes in metastatic niches. Trends Cell Biol. 2022, 32, 110–123.
  16. Lu, P.; Weaver, V.M.; Werb, Z. The extracellular matrix: A dynamic niche in cancer progression. J. Cell Biol. 2012, 196, 395–406.
  17. Anand, U.; Dey, A.; Singh Chandel, A.K.; Sanyal, R.; Mishra, A.; Kumar Pandey, D.; De Falco, V.; Upadhyay, A.; Kandimalla, R.; Chaudhary, A.; et al. Cancer chemotherapy and beyond: Current status, drug candidates, associated risks and progress in targeted therapeutics. Genes Dis. 2023, 10, 1367–1401.
  18. Kifle, Z.D.; Tadele, M.; Alemu, E.; Gedamu, T.; Ayele, A.G. A recent development of new therapeutic agents and novel drug targets for cancer treatment. SAGE Open Med. 2021, 23, 1–12.
  19. Boohaker, R.J.; Lee, M.W.; Vishnubhotla, P.; Perez, J.M.; Khaled, A.R. The Use of Therapeutic Peptides to Target and to Kill Cancer Cells. Curr. Med. Chem. 2012, 19, 3794.
  20. Khongorzul, P.; Ling, C.J.; Khan, F.U.; Ihsan, A.U.; Zhang, J. Antibody-drug conjugates: A comprehensive review. Mol. Cancer Res. 2020, 18, 3–19.
  21. Labrijn, A.F.; Janmaat, M.L.; Reichert, J.M.; Parren, P.W.H.I. Bispecific antibodies: A mechanistic review of the pipeline. Nat. Rev. Drug Discov. 2019, 18, 585–608.
  22. Muthiah, G.; Jaiswal, A. Can the Union of Prodrug Therapy and Nanomedicine Lead to Better Cancer Management? Adv. NanoBiomed Res. 2022, 2, 2100074.
  23. Kashkooli, F.M.; Soltani, M.; Hamedi, M.-H. Drug delivery to solid tumors with heterogeneous microvascular networks: Novel insights from image-based numerical modeling. Eur. J. Pharm. Sci. 2020, 151, 105399.
  24. Wu, M.; Frieboes, H.B.; Chaplain, M.A.J.; McDougall, S.R.; Cristini, V.; Lowengrub, J.S. The effect of interstitial pressure on therapeutic agent transport: Coupling with the tumor blood and lymphatic vascular systems. J. Theor. Biol. 2014, 355, 194–207.
  25. Lim, Z.-F.; Ma, P.C. Emerging insights of tumor heterogeneity and drug resistance mechanisms in lung cancer targeted therapy. J. Hematol. Oncol. 2019, 12, 134.
  26. Sarkar, S.; Levi-Polyachenko, N. Conjugated polymer nano-systems for hyperthermia, imaging and drug delivery. Adv. Drug Deliv. Rev. 2020, 163–164, 40–64.
  27. Liao, J.; Jia, Y.; Wu, Y.; Shi, K.; Yang, D.; Li, P.; Qian, Z. Physical-, chemical-, and biological-responsive nanomedicine for cancer therapy. WIREs Nanomed. Nanobiotechnol. 2020, 12, e1581.
  28. Granja, A.; Pinheiro, M.; Sousa, C.T.; Reis, S. Gold nanostructures as mediators of hyperthermia therapies in breast cancer. Biochem. Pharmacol. 2021, 190, 114639.
  29. Angelopoulou, A.; Voulgari, E.; Kolokithas-Ntoukas, A.; Bakandritsos, A.; Avgoustakis, K. Magnetic Nanoparticles for the Delivery of Dapagliflozin to Hypoxic Tumors: Physicochemical Characterization and Cell Studies. AAPS PharmSciTech 2018, 19, 2.
  30. Seynhaeve, A.L.B.; Amin, M.; Haemmerich, D.; van Rhoon, G.C.; ten Hagen, T.L.M. Hyperthermia and smart drug delivery systems for solid tumor therapy. Adv. Drug Deliv. Rev. 2020, 163–164, 125–144.
  31. Majumder, N.; Das, N.G.; Das, S.K. Polymeric micelles for anticancer drug delivery. Ther. Deliv. 2020, 11, 613–635.
  32. Perez-Herrero, E.; Fernandez-Medarde, A. Advanced targeted therapies in cancer: Drug nanocarriers, the future of chemotherapy. Eur. J. Pharm. Biopharm. 2015, 93, 52–79.
  33. Klein, O.; Kee, D.; Markman, B.; Carlino, M.S.; Underhill, C.; Palmer, J.; Power, D.; Cebon, J.; Behren, A. Evaluation of TMB as a predictive biomarker in patients with solid cancers treated with anti-PD-1/CTLA-4 combination immunotherapy. Cancer Cell 2021, 39, 592–593.
  34. Marofi, F.; Motavalli, R.; Safonov, V.A.; Thangavelu, L.; Yumashev, A.V.; Alexander, M.; Shomali, N.; Chartrand, M.S.; Pathak, Y.; Jarahian, M.; et al. CAR T cells in solid tumors: Challenges and opportunities. Stem Cell Res. Ther. 2021, 12, 81.
  35. Kirtane, K.; Elmariah, H.; Chung, C.H.; Abate-Daga, D. Adoptive cellular therapy in solid tumor malignancies: Review of the literature and challenges ahead. J. ImmunoTher. Cancer. 2021, 9, e002723.
  36. Zhang, X.; Zhang, Y.; Zheng, H.; He, Y.; Jia, H.; Zhang, L.; Lin, C.; Chen, S.; Zheng, J.; Yang, Q.; et al. In Situ biomimetic Nanoformulation for metastatic cancer immunotherapy. Acta Biomater. 2021, 134, 633–648.
  37. Catalano, V.; Turdo, A.; Di Franco, S.; Dieli, F.; Todaro, M.; Stassi, G. Tumor and its microenvironment: A synergistic interplay. Semin. Cancer Biol. 2013, 23P, 522–532.
  38. Ribatti, D.; Pezzella, F. Overview on the Different Patterns of Tumor Vascularization. Cells 2021, 10, 639.
  39. Egeblad, M.; Nakasone, E.S.; Werb, Z. Tumors as organs: Complex tissues that interface with the entire organism. Dev. Cell 2010, 18, 884–901.
  40. Siemann, D.W. The Unique Characteristics of Tumor Vasculature and Preclinical Evidence for its Selective Disruption by Tumor-Vascular Disrupting Agents. Cancer Treat. Rev. 2011, 37, 63–74.
  41. Nagl, L.; Horvath, L.; Pircher, A.; Wolf, D. Tumor Endothelial Cells (TECs) as Potential Immune Directors of the Tumor Microenvironment—New Findings and Future Perspectives. Front. Cell Dev. Biol. 2020, 8, 766.
  42. Salavati, H.; Debbaut, C.; Pullens, P.; Ceelen, W. Interstitial fluid pressure as an emerging biomarker in solid tumors. BBA–Rev. Cancer 2022, 1877, 188792.
  43. Jiao, D.; Cai, Z.; Choksi, S.; Ma, D.; Choe, M.; Kwon, H.-J.; Baik, J.Y.; Rowan, B.G.; Liu, C.; Liu, Z.-G. Necroptosis of tumor cells leads to tumor necrosis and promotes tumor metastasis. Cell Res. 2018, 28, 868–870.
  44. Seok Youn, Y.; Han Bae, Y. Perspectives on the past, present, and future of cancer nanomedicine. Adv. Drug Deliv. Rev. 2018, 130, 3–11.
  45. Al-Abd, A.M.; Aljehani, Z.K.; Gazzaz, R.W.; Fakhri, S.H.; Jabbad, A.H.; Alahdal, A.M.; Torchilin, V.P. Pharmacokinetic strategies to improve drug penetration and entrapment within solid tumors. J. Control. Release 2015, 219, 269–277.
  46. Lammers, T.; Kiessling, F.; Ashford, M.; Hennink, W.; Crommelin, D.; Storm, G. Cancer nanomedicine: Is targeting our target? Nat. Rev. Mater. 2016, 1, 16069.
  47. Wu, J. The Enhanced Permeability and Retention (EPR) Effect: The Significance of the Concept and Methods to Enhance Its Application. J. Pers. Med. 2021, 11, 771.
  48. Nicolas-Boluda, A.; Silva, A.K.A.; Fournei, S.; Gazeau, F. Physical oncology: New targets for nanomedicine. Biomaterials 2018, 150, 87–99.
  49. Dhaliwal, A.; Zheng, G. Improving accessibility of EPR-insensitive tumor phenotypes using EPR-adaptive strategies: Designing a new perspective in nanomedicine delivery. Theranostics 2019, 9, 8091–8108.
  50. Dai, W.; Wang, X.; Song, G.; Liu, T.; He, B.; Zhang, H.; Wang, X.; Zhang, Q. Combination antitumor therapy with targeted dual-nanomedicines. Adv. Drug Deliv. Rev. 2017, 115, 23–45.
  51. Danhier, F. To exploit the tumor microenvironment: Since the EPR effect fails in the clinic, what is the future of nanomedicine? J. Control. Release 2016, 244, 108–121.
  52. Khot, V.M.; Salunkhe, A.B.; Pricl, S.; Bauer, J.; Thorat, N.D.; Townley, H. Nanomedicine-driven molecular targeting, drug delivery, and therapeutic approaches to cancer chemoresistance. Drug Discov. Today 2021, 26, 724–739.
  53. Ang, M.J.Y.; Chan, S.Y.; Goh, Y.-Y.; Luo, Z.; Lau, J.W.; Liu, X. Emerging strategies in developing multifunctional nanomaterials for cancer nanotheranostics. Adv. Drug Deliv. Rev. 2021, 178, 113907.
  54. Anjali Das, C.G.; Ganesh Kumar, V.; Stalin Dhas, T.; Karthick, V.; Vineeth Kumar, C.M. Nanomaterials in anticancer applications and their mechanism of action—A review. Nanomed. Nanotechnol. Biol. Med. 2023, 47, 102613.
  55. Souri, M.; Soltani, M.; Kashkooli, F.M.; Shahvandi, M.K. Engineered strategies to enhance tumor penetration of drug-loaded nanoparticles. J. Control. Release 2022, 341, 227–246.
  56. Fulton, M.D.; Najahi-Missaoui, W. Liposomes in Cancer Therapy: How Did We Start and Where Are We Now. Int. J. Mol. Sci. 2023, 24, 6615.
  57. Rodriguez, F.; Caruana, P.; De la Fuente, N.; Espanol, P.; Gamez, M.; Balart, J.; Llurba, E.; Rovira, R.; Ruiz, R.; Martín-Lorente, C.; et al. Nano-Based Approved Pharmaceuticals for Cancer Treatment: Present and Future Challenges. Biomolecules 2022, 12, 784.
  58. Choo, H.; Jeon, S.I.; Ahn, C.-H.; Shim, M.K.; Kim, K. Emerging Albumin-Binding Anticancer Drugs for Tumor-Targeted Drug Delivery: Current Understandings and Clinical Translation. Pharmaceutics 2022, 14, 728.
  59. Pallerla, S.; Abdul, A.R.M.; Comeau, J.; Jois, S. Cancer Vaccines, Treatment of the Future: With Emphasis on HER2-Positive Breast Cancer. Int. J. Mol. Sci. 2021, 22, 779.
  60. Micale, N.; Molonia, M.S.; Citarella, A.; Cimino, F.; Saija, A.; Cristami, M.; Speciale, A. Natural Product-Based Hybrids as Potential Candidates for the Treatment of Cancer: Focus on Curcumin and Resveratrol. Molecules 2021, 26, 4665.
  61. George, A.; Shah, P.A.; Shrivastav, P.S. Natural biodegradable polymers based nano-formulations for drug delivery: A review. Int. J. Pharm. 2019, 561, 244–264.
  62. Tong, X.; Pan, W.; Su, T.; Zhang, M.; Dong, W.; Qi, X. Recent advances in natural polymer-based drug delivery systems. React. Funct. Polym. 2020, 148, 104501.
  63. Van Vierken, L.E.; Amiji, M.M. Multi-functional polymeric nanoparticles for tumour-targeted drug delivery. Expert Opin. Drug Deliv. 2006, 3, 205.
  64. Kuang, Y.; Zhai, J.; Xiao, Q.; Zhao, S.; Li, C. Polysaccharide/mesoporous silica nanoparticle-based drug delivery systems: A review. Int. J. Biol. Macromol. 2021, 193, 457.
  65. Wu, P.; Han, J.; Gong, Y.; Liu, C.; Yu, H.; Xie, N. Nanoparticle-Based Drug Delivery Systems Targeting Tumor Microenvironment for Cancer Immunotherapy Resistance: Current Advances and Applications. Pharmaceutics 2022, 14, 1990.
  66. Prajapati, S.K.; Jain, A.; Jain, A.; Jain, S. Biodegradable polymers and constructs: A novel approach in drug delivery. Eur. Polym. J. 2019, 120, 109191.
  67. Fathi, M.; Abdolahinia, E.D.; Bara, J.; Omidi, Y. Smart stimuli-responsive biopolymeric nanomedicines for targeted therapy of solid tumors. Nanomedicine 2020, 15, 2171–2200.
  68. Salavati, H.; Soltani, M.; Amanpour, S. The pivotal role of angiogenesis in a multi-scale modeling of tumor growth exhibiting the avascular and vascular phases. Microvasc. Res. 2018, 119, 105–116.
  69. Aguilar-Cazares, D.; Chavez-Dominguez, R.; Carlos-Reyes, A.; Lopez-Camarillo, C.; Hernadez de la Cruz, O.N.; Lopez-Gonzalez, J.S. Contribution of Angiogenesis to Inflammation and Cancer. Front. Oncol. 2019, 9, 1399.
  70. Al-Ostoot, F.H.; Salah, S.; Khamees, H.A.; Khanum, S.A. Tumor angiogenesis: Current challenges and therapeutic opportunities. Cancer Treat. Res. Commun. 2021, 28, 100422.
  71. Teleanu, R.I.; Chircov, C.; Grumezescu, A.M.; Teleanu, D.M. Tumor Angiogenesis and Anti-Angiogenic Strategies for Cancer Treatment. J. Clin. Med. 2020, 9, 84.
  72. Fu, L.-Q.; Du, W.-L.; Cai, M.-H.; Yao, J.-Y.; Zhao, Y.-Y.; Mou, X.-Z. The roles of tumor-associated macrophages in tumor angiogenesis and metastasis. Cell. Immun. 2020, 353, 104119.
  73. Ni, Y.; Zhou, X.; Yang, J.; Shi, H.; Li, H.; Zhao, X.; Ma, X. The Role of Tumor-Stroma Interactions in Drug Resistance Within Tumor Microenvironment. Front. Cell Dev. Biol. 2021, 9, 637675.
  74. Xu, M.; Zhang, T.; Xia, R.; Wei, Y.; Wei, X. Targeting the tumor stroma for cancer therapy. Mol. Cancer 2022, 21, 208.
  75. Zhao, X.; He, Y.; Chen, H. Autophagic tumor stroma: Mechanisms and roles in tumor growth and progression. Int. J. Cancer. 2013, 132, 1–8.
  76. Simsek, H.; Klotzsch, E. The solid tumor microenvironment Breaking the barrier for T cells How the solid tumor microenvironment influences T cells. BioEssays 2022, 44, 2100285.
  77. Gargalionis, A.N.; Papavassiliou, K.A.; Papavassiliou, A.G. Mechanobiology of solid tumors. BBA–Mol. Basis Dis. 2022, 1868, 166555.
  78. Rianna, C.; Kumar, P.; Radmacher, M. The role of the microenvironment in the biophysics of cancer. Semin. Cell Dev. Biol. 2018, 73, 107–114.
  79. Abyaneh, H.S.; Regenold, M.; McKee, T.D.; Allen, C.; Gauthier, M.A. Towards extracellular matrix normalization for improved treatment of solid tumors. Theranostics 2020, 10, 1960–1980.
  80. Cheng, B.; Yu, Q.; Wang, W. Intimate communications within the tumor microenvironment: Stromal factors function as an orchestra. J. Biomed. Sci. 2023, 30, 1.
  81. Li, Z.; Zheng, Z.; Li, C.; Li, Z.; Wu, J.; Zhang, B. Therapeutic drugs and drug delivery systems targeting stromal cells for cancer therapy: A review. J. Drug Deliv. 2020, 28, 714–726.
  82. Hurtado, P.; Martinez-Pena, I.; Pineiro, R. Dangerous Liaisons: Circulating Tumor Cells (CTCs) and Cancer-Associated Fibroblasts (CAFs). Cancers 2020, 12, 2861.
  83. Chen, X.; Song, E. Turning foes to friends: Targeting cancer- associated fibroblasts. Nat. Rev. Drug Discov. 2019, 18, 99–115.
  84. Shahvali, S.; Rahiman, N.; Jaafari, M.R.; Arabi, L. Targeting fibroblast activation protein (FAP): Advances in CAR-T cell, antibody, and vaccine in cancer immunotherapy. Drug Deliv. Transl. Res. 2023, 13, 2041–2056.
  85. Mao, Y.; Keller, E.T.; Garfield, D.H.; Shen, K.; Wang, J. Stromal cells in tumor microenvironment and breast cancer. Cancer Metastasis Rev. 2013, 32, 303–315.
  86. Li, F.; Zhao, S.; Wei, C.; Hu, Y.; Xu, T.; Xin, X.; Zhu, T.; Shang, L.; Ke, S.; Zhou, J.; et al. Development of Nectin4/FAP-targeted CAR-T cells secreting IL-7, CCL19, and IL-12 for malignant solid tumors. Front. Immunol. 2022, 13, 958082.
  87. Garcia-Bermudez, J.; Williams, R.T.; Guarecuco, R.; Birsoy, K. Targeting extracellular nutrient dependencies of cancer cells. Mol. Metab. 2020, 33, 67–82.
  88. Horsman, M.R.; Sorensen, B.S.; Busk, M.; Siemann, D.W. Therapeutic Modification of Hypoxia. Clin. Oncol. 2021, 33, e492–e509.
  89. McAleese, C.E.; Choudhury, C.; Butcher, N.J.; Minchin, R.F. Hypoxia-mediated drug resistance in breast cancers. Cancer Lett. 2021, 502, 189–199.
  90. Khoshinani, H.M.; Afshar, S.; Najafi, R. Hypoxia: A Double-Edged Sword in Cancer Therapy. Cancer Investig. 2016, 34, 536–545.
  91. Wiechec, E.; Matic, N.; Ali, A.; Roberg, K. Hypoxia induces radioresistance, epithelial-mesenchymal transition, cancer stem cell-like phenotype and changes in genes possessing multiple biological functions in head and neck squamous cell carcinoma. Oncol. Rep. 2022, 47, 58.
  92. Razi, S.; Haghparast, A.; Khameneh, S.C.; Sadrabadi, A.E.; Aziziyan, F.; Bakhtiyari, M.; Nabi-Afjadi, M.; Tarhriz, V.; Jalili, A.; Zalpoor, H. The role of tumor microenvironment on cancer stem cell fate in solid tumors. Cell Commun. Signal. 2023, 21, 143.
  93. Vaupel, P.; Multhoff, G. Fatal Alliance of Hypoxia-/HIF-1α-Driven Microenvironmental Traits Promoting Cancer Progression. In Oxygen Transport to Tissue XLI; Advances in Experimental Medicine and, Biology; Ryu, P.D., LaManna, J., Harrison, D., Lee, S.S., Eds.; Springer: Cham, Switzerland, 2020; Volume 1232.
  94. Kes, M.M.G.; Van den Bossche, J.; Griffioen, A.W.; Huijbers, E.J.M. Oncometabolites lactate and succinate drive pro-angiogenic macrophage response in tumors. BBA–Rev. Cancer 2020, 1874, 188427.
  95. Singh, L.; Nair, L.; Kumar, D.; Arora, M.K.; Bajaj, S.; Gadewar, M.; Mishra, S.S.; Rath, S.K.; Dubey, A.K.; Kaithwas, G.; et al. Hypoxia induced lactate acidosis modulates tumor microenvironment and lipid reprogramming to sustain the cancer cell survival. Front. Oncol. 2023, 13, 1034205.
  96. Wang, J.; Matisevic, S. Functional and metabolic targeting of natural killer cells to solid tumors. Cell. Oncol. 2020, 43, 577–600.
  97. Chen, C.; Wang, Z.; Ding, Y.; Qin, Y. Manipulating T-cell metabolism to enhance immunotherapy in solid tumor. Front. Immunol. 2022, 13, 1090429.
  98. Goswami, K.K.; Banerjee, S.; Bose, A.; Baral, R. Lactic acid in alternative polarization and function of macrophages in tumor microenvironment. Hum. Immunol. 2022, 83, 409–417.
  99. Koltai, T. The complex relationship between multiple drug resistance and the tumor pH gradient: A review. Cancer Drug Resist. 2022, 5, 277.
  100. Vaidya, F.U.; Chhipa, A.S.; Mishra, V.; Gupta, V.K.; Rawat, S.G.; Kumar, A.; Pathak, C. Molecular and cellular paradigms of multidrug resistance in cancer. Cancer Rep. 2022, 5, e1291.
  101. AlSawaftah, N.M.; Awad, N.S.; Pitt, W.G.; Husseini, G.A. pH-Responsive Nanocarriers in Cancer Therapy. Polymers 2022, 14, 936.
  102. Zhou, W.; Jia, Y.; Liu, Y.; Chen, Y.; Zhao, P. Tumor Microenvironment-Based Stimuli-Responsive Nanoparticles for Controlled Release of Drugs in Cancer Therapy. Pharmaceutics 2022, 14, 2346.
  103. Yan, Y.; Ding, H. pH-Responsive Nanoparticles for Cancer Immunotherapy: A Brief Review. Nanomaterials 2020, 10, 1613.
  104. Lim, E.-K.; Chung, B.H.; Chung, S. Recent Advances in pH-Sensitive Polymeric Nanoparticles for Smart Drug Delivery in Cancer Therapy. Curr. Drug Targets 2018, 19, 300.
  105. Sethuraman, V.; Janakiraman, K.; Krishnaswami, V.; Kandasamy, R. Recent Progress in Stimuli-Responsive Intelligent Nano Scale Drug Delivery Systems: A Special Focus Towards pH-Sensitive Systems. Curr. Drug Targets 2021, 22, 947.
  106. Corbet, C.; Feron, O. Tumour acidosis: From the passenger to the driver’s seat. Nat. Rev. Cancer 2017, 17, 577.
  107. Wang, C.; Ding, S.; Wang, S.; Shi, Z.; Pandey, N.K.; Chudal, L.; Wang, L.; Zhang, Z.; Wen, Y.; Yao, H.; et al. Endogenous tumor microenvironment-responsive multifunctional nanoplatforms for precision cancer theranostics. Coord. Chem. Rev. 2021, 426, 213529.
  108. Ruan, S.; Huang, Y.; He, M.; Gao, H. Advanced Biomaterials for Cell-Specific Modulation and Restore of Cancer Immunotherapy. Adv. Sci. 2022, 9, 2200027.
  109. Cai, L.; Xu, J.; Yang, Z.; Tong, R.; Dong, Z.; Wang, C.; Leong, K.W. Engineered biomaterials for cancer immunotherapy. Med. Comm. 2020, 1, 35.
  110. Xie, Y.-Q.; Wei, L.; Tang, L. Immunoengineering with biomaterials for enhanced cancer immunotherapy. WIREs Nanomed. Nanobiotechnol. 2018, 10, e1506.
  111. Bo, Y.; Wang, H. Biomaterial-Based In Situ Cancer Vaccines. Adv. Mater. 2023, 2210452.
  112. Abdou, P.; Wang, Z.; Chen, Q.; Chan, A.; Zhou, D.R.; Gunadhi, V.; Gu, Z. Advances in engineering local drug delivery systems for cancer immunotherapy. WIREs Nanomed. Nanobiotechnol. 2020, 12, e1632.
  113. Hu, L.; Cao, Z.; Ma, L.; Liu, Z.; Liao, G.; Wang, J.; Shen, S.; Li, D.; Yang, X. The potentiated checkpoint blockade immunotherapy by ROS-responsive nanocarrier-mediated cascade chemo-photodynamic therapy. Biomaterials 2019, 223, 119469.
  114. Wang, C.; Ye, Y.; Hu, Q.; Bellotti, A.; Gu, Z. Tailoring Biomaterials for Cancer Immunotherapy: Emerging Trends and Future Outlook. Adv. Mater. 2017, 29, 1606036.
  115. Rosalia, R.A.; Cruz, L.J.; van Duikeren, S.; Tromp, A.T.; Silva, A.L.; Jiskoot, W.; de Gruijl, T.; Lowik, C.; Oostendorp, J.; van der Burg, A.; et al. CD40-targeted dendritic cell delivery of PLGA-nanoparticle vaccines induce potent anti-tumor responses. Biomaterials 2015, 40, 88.
  116. Wang, C.; Li, P.; Liu, L.I.; Pan, H.; Li, H.; Cai, L.; Ma, Y. Self-adjuvanted nanovaccine for cancer immunotherapy: Role of lysosomal rupture-induced ROS in MHC class I antigen presentation. Biomaterials 2016, 79, 88.
  117. Yan, S.; Luo, Z.; Li, Z.; Wang, Y.; Tao, J.; Gong, C.; Liu, X. Improving Cancer Immunotherapy Outcomes Using Biomaterials. Angew. Chem. 2020, 132, 17484.
  118. Yang, J.; Zhang, C. Regulation of cancer-immunity cycle and tumor microenvironment by nanobiomaterials to enhance tumor immunotherapy. WIREs Nanomed. Nanobiotechnol. 2020, 12, e1612.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
Upload a video for this entry
Information
Subjects: Medicine, Research & Experimental
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Konstantinos Avgoustakis
,
Athina Angelopoulou
View Times: 217
Entry Collection: Biopharmaceuticals Technology
Revisions: 6 times (View History)
Update Date: 17 Feb 2024
Table of Contents
    1000/1000
    Hot Most Recent
    Feedback