Flavonoids for Breast Cancer: History
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Breast cancer persists as a diffuse source of cancer despite persistent detection and treatment. Flavonoids, a type of polyphenol, appear to be a productive option in the treatment of breast cancer, because of their capacity to regulate the tumor related functions of class of compounds. Plant polyphenols are flavonoids that appear to exhibit properties which are beneficial for breast cancer therapy. Numerous epidemiologic studies have been performed on the dynamic effect of plant polyphenols in the prevention of breast cancer. There are also subclasses of flavonoids that have antioxidant and anticarcinogenic activity. These can regulate the scavenging activity of reactive oxygen species (ROS) which help in cell cycle arrest and suppress the uncontrolled division of cancer cells. Numerous studies have also been performed at the population level, one of which reported a connection between cancer risk and intake of dietary flavonoids. Breast cancer appears to show intertumoral heterogeneity with estrogen receptor positive and negative cells.

  • flavonoids
  • nanoparticles
  • breast cancer
  • drug delivery system
  • cancer therapeutics
  • anticancer
  • phytochemicals
  • apoptosis
  • epidemiological study

1. Introduction

Cancer is an inherited disease provoked by changes in the genetic code that regulate the functioning of cells, and is a crucial health complication over the world [1]. The incidence of cancer has increasing during the previous few years, but has decreased due to advancements in the treatment of cancer [2]. Epigenetic and genetic factors may cause the formation of tumor cells and their proliferation [3]. It is due to atypical growth of cells and has the potential to interfere with normal cell growth [4]. Cancer can also be described as a multiplex process that hinders the growth of normal cells, causes inexhaustible cell expansion, and changes the physiology of cells that can cause malignant cancer [5]. Studies of cancer have concluded that itis due to both environmental and genetic factors [6]. Physiological factors of cancer include hypoxia, insufficiency of genetic mutations, programmed cell death function, and oxidative stress, while apparent causes include pollution, radiation, and chronic exposure to ultraviolet rays [7]. The most common cancer among women is breast cancer which has a high death rate [8]. About 1.5 million cases of breast cancer occur worldwide each year [8]. About 1.7 million new instances were identified in the year 2012 [9].
The American Cancer Society estimated that about 281,550 new cases of breast cancer will be recognized in women in 2021. There are many kinds of breast cancer, but the most common are invasive carcinoma and ductal carcinoma in situ (DCIS). Others, such as angiosarcoma and phyllodes tumors, are less common [10]. The National Cancer Institute (NCI) has stated that avoidance is an effective means of reducing the number of individuals affected by cancer [11]. Most cancer preventive agents and anatomical administered breast cancer drugs are made to target only cancerous breast cells. Other healthy tissues may suffer from noxious effects. Studies concluded that flavonoids such as fucoidan could instigate cell cycle arrest [12]. Epidemic research and methodical examination have concluded that diets rich in vegetables and fruits are correlated with decreased risk of cancer originating in the epithelium such as mouth and breast. [13][14]. More intake of vegetables and fruits decreases the chances of cancer, including breast cancer [15][16]. Studies suggest that naturally produced compounds can have cancer preventive properties [17].
Flavonoids are polyphenolic compounds produced in plants in the form of bioactive secondary metabolites. Flavonoids consist of the flavone structure 15-C chain of phenylpropanoids. There are various types of flavonoids such flavanol and flavones. The capacity of flavonoids to restrain the metabolism of cells and to scrounge free radicals are reported in a number of studies [18]. Flavonoids are used in breast cancer treatment as antioxidants and by acting in macrophages by obstructing the formation of ROS (Reactive Oxygen Species), showing an immune modulating effect. The capacity of the flavonoids to select macrophages function to lower conditions such as immunosuppression of TMC in breast cancer [19].
Major research has been done on the efficacy of flavonoids such as quercetin, silibinin, apigenin, epigallocatechin-3-gallate, genistein, kaempferol, and naringenin against different cancer types, but due to poor absorption, low solubility, and easy metabolism, utilization of polyphenols in treatment of cancer is not sufficient. In this regard, current nanotechnology may be employed [20].
There are many types of polyphenols nanocarriers recently employed in the treatment of cancer. These include nanocapsules [21], solid lipid nanocarriers, nanoparticles [22], and metallic nanoparticles (gold) [23]. Selection of these techniques for nanoformulation leads to enhancement in biodistribution, pharmacokinetics, bioavailability, and specificity of drug transport to the site of cancer [24]. The applications of nanodelivery are discussed in Figure 1.
Figure 1. Benefits of nanodelivery systems.
Among the naturally occurring compounds, flavonoids have been recorded to have anticancer properties [25][26][27]. Patients of breast cancer can be recognized by radiation therapy, hormone therapy, surgery, natural therapy, and chemotherapy. These remedies are used to control and prevent the development of metastatic tumors [28].

2. Flavonoids Used in Breast Cancer

Flavonoids are categorized into various groups on the basis of carbon in the C ring, unsaturation, and oxidation of the C ring. The subcategories are discussed in Table 1:
Table 1. Various types of flavonoids.
NO. FLAVONOIDS CONSTITUENTS
1 FLAVONES Consist of apigenin, tangeretin, luteolin, chrysin [29]
2 FLAVONOLS Consist of quercetin, isorhamnetin, myricetin, kaempferol [30]
3 FLAVONOIDS Consist of naringenin, eriodictyol, hesperidin
4 CATECHINS Consist of epicatechin, epigallocatechin gallate, (−)-epicatechingallate (ECG), (−)-epigallocatechin found in tea leaves
5 ISOFLAVONES Consist of biochanin A, phytoestrogens, genistein, formononetin, daidzein
6 ANTHOCYANIDINS Pelargonidin, cyanidin, malvidin, delphinidin, peonidin, petunidin
7 PROCYANIDINS These are the oligomers of epicatechin, gallic acid, esters and catechin
8 LIGNANS Plant components absorbed in gut to form phytoestrogens, enterolactone, enterodiol
9 FLAVAN-3-OLS Consist of catechin, epicatechin, epigallocatechin, theaflavin-3-gallate, theaflavin-3,3′-digallic acid [29][31]

2.1. Flavones

Flavones generally exist in leaves, fruits, and flowers such as glycosides [30]. The chemical structure of flavones shown in Figure 3. They show a number of activities such as antioxidant, antiviral, and anticancer properties. Flavones consist of apigenin, nobiletin, luteolin, tangeretin, chrysin, and baicalein. Flavones are widely studied as anticancer agents and work by inhibiting tumor enlargement in the cells of cancer by the process of apoptosis [32]. They have no adverse effects.
Figure 3. Flavone.
In human cancer cells including prostate and melanoma, luteolin exhibits arrest of the cell cycle whereas dis-arrest produced by luteolin is associated with suppression of CDA2 activity in colorectal cancer. Luteolin also represses the function of the epidermal growth factor (EHFR) breast cancer cell line in humans [33]. Luteolin decreases the progression of MPA-dependent breast cancer cell allograft.
Luteolin initiates the process of apoptosis in breast cancer cells by the inhibition of fatty acid synthesis which is an essential lipogenic enzyme overexposed in many human cancers [34].

2.2. Flavonols

Flavonols are the main sub-category of flavonoid, that have the 3-hydroxyflavone backbone shown in Figure 4. They are found in onions, tea, some common fruits, and broccoli. Flavanols such as isorhamnetin, kaempferol, quercetin, and myricetin are some examples [35]. Flavonols may inhibit breast carcinogenesis. Flavonols may be pro-oxidant, antioxidant, anti-estrogenic, or modulate of cell signaling pathways. A recent analysis of flavonoid consumption and breast cancer recommended that flavonols and dietary flavonoids are linked with a lower risk of breast cancer, mainly in post-menopausal women [36].
Figure 4. Flavonol.
Quercetin is a glycoside found mainly in onions, apples, and garlic can initiate damage of DNA in cancer cells [37]. Current research shows that quercetin plays a pivotal role in inhibiting transduction of signals, apoptosis in cancer cells and by suppressing the multiplication of tumor cells [38][39][40]. Kaempferol plays an important role in the inhibition of growth of breast cancer cell lines. Flavones are a major class of flavonoid and are mainly found in citrus fruits such as lemons, grapefruit, and oranges. Naringenin, eriodictyol, and hesperidin are examples of flavanones. Flavanone containing citrus has pharmacological effects such as anti-inflammatory, cholesterol lowering, antioxidant, and blood lipid lowering activity [41]. Citrus juices are procured from blond oranges, grapefruit, mandarins, sour oranges, lemons, tangors, bergamots, tangerines, limes, kumquats, etc., the major constituent in blond oranges is 200–600 mg/L of hesperidin but they also contain didymin (19–35 mg/L) and narirutin (16–84 mg/L). Hesperidin is also the predominant compound in lemon juice and lime [42].
Hesperidin, an inhibitor of aromatase and a main curative agent for estrogen receptor positive breast cancer in perimenopausal women has also shown to be an inhibitor of enlargement of MDA-MB231 cells, probably due to glucose uptake deterioration and repression of glucose transporter1(GLUT-1). Narigenin, also a flavanone, is a weak estrogen and appears to be used in lowering the P38 MAPK pathway. It suppresses metastasis of lung in breast cancer patients after surgery by stimulating immunity in the host by an extension of Interleukin (IL-2) T cells and Interferon (INF)-alpha [43].

2.3. Catechins

Catechin is a flavonoid which was mainly found in tea leaves. It comprises a set of polyphenols that contains catechin various health benefits. Epigallocatechin gallate (EGCG), epicatechin (EC), epigallocatechin (EGC), and epicatechin gallate (ECG) are the vital catechins found in tea leaves [44]. In vitro and epidemiological studies of catechin associated with green tea produce depression in breast cancer patients [45]. Consumption of green tea was not related to the general risk of breast cancer [46]. However, the reaction of tea and its catechins on the diagnosis of breast cancer are still unknown [47][48].
Tea and tea polyphenol have been studied for the last two decades with emphasis on the prospective cancer chemo preventive and medicinal properties of teas. Present data suggest a strong chemopreventive and therapeutic effect of green tea polyphenols and EGCG against cancer of the skin, breast, liver, prostate, colon, lung, and liver [49]. In Asian countries, epidemiological scrutiny has recommended that the lower occurrence of some cancers is because of the consumption of green tea [50].

2.4. Isoflavones

Isoflavones are polyphenolic and they mainly present in soybeans which area rich source of protein for millions of individuals. The chemical structure of isoflavones shown in Figure 5. Soybean contains isoflavones, which are phytoestrogen polyphenols with vigorous anticancer effects. Soybean rich isoflavones are an anticancer compound, soy foods contain many bioactive compounds such as lunasin, omega-3-fatty acid, Bowman–Birk inhibitor, and dietary fiber. Soy foods are used in the prevention of diabetes, cardiovascular disease, hypertension, and cancer [51][52][53][54].
Figure 5. Isoflavone.
Daidzein, genistein, and biochanin A are formononetin phytoestrogens. A rich source of isoflavones are legumes from the family Fabaceae [55]. Soybean (Glycine max), such as glycitein, daidzein, genistein, and red clover (Trifolium pratense), has an etymology from biochanin A and formononetin. Daidzein and genistein are the most known isoflavones because of their estrogenic effect in animal models.

2.5. Anthocyanidins

Anthocyanins are abundantly found in plants and are a category of flavonoids. They are present in various fruits and flowers such as grapes, strawberries, and corn, and can exhibit purple, blue, or red color. Anthocyanins have a number of properties such as bacteriostatic, anti-aging, anticancer, and anti-inflammatory activities.
They work by inducing differentiation, a process in which malignant cells differentiate into normal mature cells by the inducers [56].
Anthocyanins can stop the proliferation of cancer cells in three ways:
(1)
Signal pathway inhibition for blocking of signal transduction.
(2)
Regulation of antioncogenes.
(3)
By acting on beta-catechin, Notch pathway.
Anthocyanidin and its extract have manifested anti-cell multiplication outcomes regarding distinct types of breast cancer cells [17][18]. Examples include, Anthocyanins isolated from Mix Eco Blue corn, which retards the proliferation of cells by arresting the cell cycle at G1 phase.
Another study shows an extract of anthocyanins from strawberry inhibited the multiplication of cell on breast cancer cell lines in murine [18].
They were initiated to inhibit cancer cells by lowering the expression of Matrix Metalloproteinase (MMP) and urokinase plasminogen activator, which deteriorate the extracellular matrix as an invasion process by restoring the expression of inhibition, both of which nullify MPA and MPP action [57].
In one study, when treatment was done with P3G and C3G sensitive Transtuzumab resistant MDA-M-53 R which initiates process of apoptosis, inhibition of p-HER 2 and P Marks took place and showed inhibition of human breast cancer in vitro [58].

3. Nano-Based Formulation of Phyto-Bioactive Used in Breast Cancer Prevention

Currently, there has been extensive growth in the area of nano based delivery to transport innate forms of vital substances and medicinal agents for the therapy of different diseases [59].
One main complication in the study is that expanding multipurpose nanomolecules have effects which permit them to carry individual curatives across different biological hurdles and are suitable to mark specific cells, organs, and tissues in the body. Between different nanodelivery systems, there are both polymeric nanocrystals, solid types such as lipids and nanoparticles, and liquid types, such as nanoemulsions, nanopolymers, and nanoliposomes [60]. There are different nanomaterials that are used in the delivery of drugs. These nano phyto-bioactive and their properties are described below.

3.1. Nano-Curcumin

Curcumin is a diarylheptanoid, polyphenol (shown in Figure 9) extracted from the root of the turmeric plant, acquired from ferulic acid, and segregated from the Indian plant Curcuma longa (Zingiberaceae). It has antineoplastic, antifungal, and antibacterial properties. US FDA(GRN-686) have approved this plant as Generally Recognized as Safe (GRAS) [61].
Figure 9. Curcumin.
The use of curcumin in the targeting and prevention of different aging related pathological situations has been frequently recorded [62]. These states consist of inflammation, cardiovascular disease, oxidative stress, type-2 diabetes, rheumatoid arthritis, ocular disease, atherosclerosis, osteoporosis, neurodegenerative diseases, and cancer. From the last decade, the possibility of this compound to enhance therapeutic effectiveness has been examined in clinical trials [63].
Along with therapeutic activities, a vital problem with curcumin is the bioavailability due to its low solubility in aqueous solution which limits clinical efficacy. To overcome the problem, nanocarriers for curcumin have been developed. Overdose of drugs is still a common clinical issue across the world, taking place both intentionally and unintentionally. Antidotes exist, but are not easily available. Therefore, nanoparticles have been formulated for delivery of many drugs [64].
Clinical trials have been performed for the treatment of different types of cancers such as pancreatic, prostate, and breast cancer. The various nano flavonoids used in the treatment of breast cancer are described in Figure 10.
Figure 10. Therapeutic potential of nano flavonoids on breast cancer.

3.2. Nano-Epigallocatechin-3-Gallate

Epigallocatechin-3-gallate [EGCG], a polyphenol(catechin) obtained from green tea, has a role as an anticancer drug [65]. It also acts as an anti-HSP90, antioxidant, neuroprotective, and neoplastic agent [66]. This medication is being clinically tested in different types of cancer therapies including lung cancer (Phase 2), prostate cancer (Phase 1), and colorectal cancer (Phase1) (NCTO2577393, NCTO459407, NCTO2891538).
An epidemiology investigation was performed to scrutinize repeatedly contrasting in vitro detecting. This uncertainty could be due to its poor bioavailability and stability. Hence, to enhance bioavailability of EGCG, new nanodelivery systems have been employed. Elevated potential and more stability for oral conveyance were available in EGCG-loaded solid lipid nanomolecules than for untreated EGCG [67].
Nanoparticles that enhance the anticancer properties of EGCG are chitin-loaded honokiol and nanoethosomes. An investigation proved that delivery of docetaxel present in EGCG-nanoethosomes transdermally diminish the volume of tumor. The nanoethosome permits flavonoids’ transdermal delivery to melanoma cancer cells [68].

3.3. Nano-Naringenin

Naringenin (NAR), a naturally present flavonoid in plants such as citrus fruits, has a great number of pharmacological activities. Its scientific occurrence has been hampered because of poor aqueous solubility and improper transport across biological membranes which lead to low bioavailability at the site of the tumor [69]. Its chemical structure shown in Figure 11.
Figure 11. Naringenin.
In contemporary studies, antiproliferative outcomes of Naringenin with cyclophosphamide were studied in breast cancer cells and involvement of JAK-2 and STAT-3 were explored. It is seen that naringenin also has the ability to repress the functions of IL-6 in regulating apoptosis-associated expression of genes. Naringenin and cyclophosphamide can impair the uncontrolled division of cells to a sustainable degree and can be distributed as potent chemotherapeutics for the treatment of breast cancer [70].
Many nanoscaled delivery systems are used, such as polymeric nanoparticles, nano suspension, and nano emulsions. Nano emulsions have an elevated ability to alter the bioavailability of drugs which are less soluble by oral route. To increase the oral bioavailability and solubility of naringenin, some papers describe the use of nanoemulsions as a system of drug delivery for NRG [71].
Nanonargenin works by inhibiting both PI3K and MAPK paths and by restricting ER alpha to the cytoplasm to lessen proliferation of Tam-RMC cells. This study demonstrates the mode required in the proliferation of cells of Tam-R breast cancer cells [72].

3.4. Nano-Quercetin

Quercetin (QT) is a pentahydroxyflavone polyphenols shown in Figure 12. It is found in red grapes, olive oil, bracken fern, lettuce, onion, tea, coffee, and citrus. QT has noxious effects on various cancer cell types. However, lesser bioavailability and deficient solubility of QT have restricted its therapeutic use [73]. QT has cytoprotective effects to hinder various molecules that are used in some signaling pathways, imparting carcinogenesis activity, and containing protein kinase-C, tyrosine kinase, and phosphatidylinositol-3 kinase. Modern research exhibits the importance of tyrosine kinase pathways in breast cancer continuance [74]. The antioxidant polyphenol quercetin can limit damage from free radical. However, quercetin, an inhibitor of lipid peroxidase, might be helpful as an anticancer cell [75]. Hence, it is demonstrated that quercetin acts as an inhibitor in the growth of the MCF-7 cell line.
Figure 12. Quercetin.
Metabolism and maintenance of blood levels in tissues is accomplished by encapsulation of quercetin for a prolonged period of time. It enhances bioavailability, solubility, and increased sustained release by nanoencapsulation, and may improve the bioactive quercetin-loaded nanomicelles that are stable in intestinal and gastric fluids [76].

3.5. Nano-Resveratrol

Resveratrol is a 5,4′-Trihydroxystilbene (Figure 13), natural polyphenol, has a range of biological properties, including antioxidant, anti-fungal, anti-aging, anti-inflammatory, and antiviral activities. Several studies have proven that RES contains chemoprotective activities such as neuroprotective- and cardioprotective effects [77]. Administration of resveratrol with chemotherapeutic agents reduces the toxic effects associated with it and enhances the medicinal efficacy related with chemotherapy of cancer.
Figure 13. Resveratrol.
Beta glucan has been utilized as a complementary carrier of drugs, or in addition with a drug such as resveratrol by using a drug delivery system to increase bioavailability. Research has recognized the synergistic effects of resveratrol and beta glucan on immune reactions. Combinational effects were examined in each case, and the potential of these compositions on gene countenance (such as Cdc42, NF-KB2 and BcL-2) in cancer cells of breast were analyzed [78].

3.6. Nano-Apigenin

Apigenin is a 4′,5,7-trihydroxyflavone as shown in Figure 14. It is a flavonoid having low molecular weight, found in plant-derived beverages, fruits, nuts, and vegetables that hinders the growth of cancer cells of humans in vivo and in vitro [79]. Apigenin has shown effects on different types of cancers such as liver cancer, prostate cancer, colorectal cancer, lung cancer, melanoma, osteosarcoma, and breast cancer [80].
Figure 14. Apigenin.
This polyphenol is used in modulating signaling pathways in skin cancer and hepatocellular carcinoma. The favorable effect of individual apigenin in the treatment of cancer is comparatively low due to its low water solubility [81]. These days, to enhance the polyphenols bioavailability, PLGA nanoparticles are mostly used.
Research shows that the bioavailability of apigenin is low. To enhance the functionality of apigenin, a nanoformulation of apigenin is under examination in in vivo and invitro models. Biosensors and gold nanoparticles (AuNPs) used in photothermal therapy have acquired marketability because of their attainable implementation in drug delivery and in the treatment of cancer [82].
Apigenin-AuNPs also show adequate antiangiogenic properties. Moreover, studies on nano-apigenin utilizing poly(lactic-co-glycoside) (PLGA) are efficacious in topical and oral administration for skin care, attaining a higher potency and efficacy with decreased toxicity. This evidence proves that nanoformulations of apigenin could enhance an essential drug-delivery system.

3.7. Nano-Silibrin

Silibrin is a flavonolignan obtained from the fruit of Silybum marianum Gaertner. Silibrin-loaded nanoparticles suppress tumor angiogenesis and the epithelial–mesenchymal transition (7). Silibrin and cryptotanshinone effectively perforate the barriers of the intestine, hence increasing the pharmacokinetic of drug loads [83].
These nanoparticles manifest beneficial anti metastasis resulting in breast cancer bearing nude mice. In order to get better results against metastasis of breast cancer, lipid nanoparticles loaded with silibrin consisting of d-alpha tocopheryl polyethylene glycol 1000 succinate, silibinin, and phosphatidylcholine were obtained [84].
Silibrin loaded nanoparticles (SLNs) can accumulate in tissues of tumor in a planned order. In comparison to free silibrin, SLNs contain many inhibitory effects in the conquering of MDA-MB—231 cells by down regulation of snail and MMP.
Nano Isomers filled with silibinin can be used as feedback in breast cancer. In one of the studies, silibinin was encapsulated in glycol and its effectiveness against cancer was checked [85].

3.8. Nano-Genistein

Genistein is a natural isoflavonoid of phytoestrogen class, abundantly found in soy, which has breast-cancer preventive properties. A recent study was conducted revealing the action responsible for the inhibitory activity of genistein in MCF-7 cells. It arrests the growth of MCF-4 cells at the M/G2 phase and lowers it at the proliferative S-phase [86].
Genistein-loaded PEGylated silica hybrid nanomaterials were produced by an efficient and simple aqueous dispersion method. Infrared analysis also found that the encapsulation of genistein was fully obtained with effectiveness in breast cancer treatment [87][88]. Various nanoformulations of flavonoids in the treatment of breast cancer with MOA are detailed in Table 2.
Table 2. Nanoformulations of flavonoids with mechanism of action in treatment breast cancer.
NO. NANOFORMULATION MECHANISM OF ACTION
1 NANO-CURCUMIN Use of curcumin in targeting and prevention of different aging related pathological situations has been recorded [61]
2 NANO-EPIGALLOCATECHIN-3-GALLATE Delivery of docetaxel present in EGCG-nanoethosomes transdermal diminish the volume of tumor [68]
3 NANO-NARINGENIN Works by inhibiting both P13K and MAPK paths also restricts ER alpha to lessen the proliferation of tam-RMC cells [72]
4 NANO-QUERCETIN It acts as growth inhibitor of MCF-7 cell lines
5 NANO-RESVERATROL Combinational effect of resveratrol and Beta-glucan potentiates the composition on gene countenance (such as cdc42, NF-KB2 and BCL-2) in breast cancer cells [78]
6 NANO-APIGENIN Biosensors used in photothermal therapy and have acquired implementation in treatment of cancer [79]
7 NANO-SILIBRIN Silibrin loaded nanoparticles (SLNs) contain inhibitory effects on conquering of MDA-MB-231 cells
8 NANO-GENISTEIN Responsible for the arrest of growth of MCF-4 cells at M/G2 phase and lower at proliferative S-phase [83]

This entry is adapted from the peer-reviewed paper 10.3390/molecules26175163

References

  1. Imran, M.; Rauf, A.; Abu-Izneid, T.; Nadeem, M.; Shariati, M.A.; Khan, I.A.; Imran, A.; Orhan, I.E.; Rizwan, M.; Atif, M.; et al. Luteolin, a flavonoid, as an anticancer agent: A review. Biomed. Pharmacother. 2019, 112, 108612.
  2. Rodríguez-García, C.; Sánchez-Quesada, C.; Gaforio, J.J. Dietary flavonoids as cancer chemopreventive agents: An updated review of human studies. Antioxidants 2019, 8, 137.
  3. Khan, H.; Ullah, H.; Martorell, M.; Valdes, S.E.; Belwal, T.; Tejada, S.; Sureda, A.; Kamal, M.A. Flavonoids nanoparticles in cancer: Treatment, prevention and clinical prospects. Semin. Cancer Biol. 2021, 69, 200–211.
  4. George, V.C.; Dellaire, G.; Rupasinghe, H.V. Plant flavonoids in cancer chemoprevention: Role in genome stability. J. Nutr. Biochem. 2017, 45, 1–4.
  5. Devi, K.P.; Rajavel, T.; Nabavi, S.F.; Setzer, W.N.; Ahmadi, A.; Mansouri, K.; Nabavi, S.M. Hesperidin: A promising anticancer agent from nature. Ind. Crop. Prod. 2015, 76, 582–589.
  6. Theodoratou, E.; Timofeeva, M.; Li, X.; Meng, X.; Ioannidis, J.P. Nature, nurture, and cancer risks: Genetic and nutritional contributions to cancer. Annu. Rev. Nutr. 2017, 37, 293–320.
  7. Abotaleb, M.; Samuel, S.M.; Varghese, E.; Varghese, S.; Kubatka, P.; Liskova, A.; Büsselberg, D. Flavonoids in cancer and apoptosis. Cancers 2019, 11, 28.
  8. He, X.; Xue, M.; Jiang, S.; Li, W.; Yu, J.; Xiang, S. Fucoidan promotes apoptosis and inhibits emt of breast cancer cells. Biol. Pharm. Bull. 2019, 42, 442–447.
  9. Beatrice Magne Nde, C.; Zingue, S.; Winter, E.; Beatriz Creczynski-Pasa, T.; Michel, T.; Fernandez, X.; Njamen, D.; Clyne, C. Flavonoids, breast cancer chemopreventive and/or chemotherapeutic agents. Curr. Med. Chem. 2015, 22, 3434–3446.
  10. Schick, J.; Ritchie, R.P.; Restini, C. Breast Cancer Therapeutics and Biomarkers: Past, Present, and Future Approaches. Breast Cancer Basic Clin. Res. 2021, 15, 1178223421995854.
  11. Chow, H.H.; Cai, Y.; Alberts, D.S.; Hakim, I.; Dorr, R.; Shahi, F.; Crowell, J.A.; Yang, C.S.; Hara, Y. Phase I pharmacokinetic study of tea polyphenols following single-dose administration of epigallocatechin gallate and polyphenon E. Cancer Epidem. Biomar. 2001, 10, 53–58.
  12. Hsu, H.Y.; Lin, T.Y.; Wu, Y.C.; Tsao, S.M.; Hwang, P.A.; Shih, Y.W.; Hsu, J. Fucoidan inhibition of lung cancer in vivo and in vitro: Role of the Smurfs 2-dependent ubiquitin proteasome pathway in TGFβ receptor degradation. Oncotarget 2014, 5, 7870.
  13. Aune, D.; Chan, D.S.; Vieira, A.R.; Rosenblatt, D.N.; Vieira, R.; Greenwood, D.C.; Norat, T. Fruits, vegetables and breast cancer risk: A systematic review and meta-analysis of prospective studies. Breast Cancer Res. Treat. 2012, 134, 479–493.
  14. Reiss, R.; Johnston, J.; Tucker, K.; DeSesso, J.M.; Keen, C.L. Estimation of cancer risks and benefits associated with a potential increased consumption of fruits and vegetables. Food Chem. Toxicol. 2012, 50, 4421–4427.
  15. Zhang, C.X.; Ho, S.C.; Chen, Y.M.; Lin, F.Y.; Fu, J.H.; Cheng, S.Z. Meat and egg consumption and risk of breast cancer among Chinese women. Cancer Causes Control 2009, 20, 1845–1853.
  16. Butler, L.M.; Wu, A.H.; Wang, R.; Koh, W.P.; Yuan, J.M.; Yu, M.C. A vegetable-fruit-soy dietary pattern protects against breast cancer among postmenopausal Singapore Chinese women. Am. J. Clin. Nutr. 2010, 91, 1013–1019.
  17. Wang, R.; Yang, L.; Li, S.; Ye, D.; Yang, L.; Liu, Q.; Zhao, Z.; Cai, Q.; Tan, J.; Li, X. Quercetin inhibits breast cancer stem cells via downregulation of aldehyde dehydrogenase 1A1 (ALDH1A1), chemokine receptor type 4 (CXCR4), mucin 1 (MUC1), and epithelial cell adhesion molecule (EpCAM). Medical Science Monitor. Int. J. Clin. Exp. Med. 2018, 24, 412.
  18. Kopustinskiene, D.M.; Jakstas, V.; Savickas, A.; Bernatoniene, J. Flavonoids as anticancer agents. Nutrients 2020, 12, 457.
  19. Sudhakaran, M.; Sardesai, S.; Doseff, A.I. Flavonoids: New frontier for immune-regulation and breast cancer control. Antioxidants 2019, 8, 103.
  20. Chen, J.; Xu, B.; Sun, J.; Jiang, X.; Bai, W. Anthocyanin supplement as a dietary strategy in cancer prevention and management: A comprehensive review. Crit. Rev. Food Sci. Nutr. 2021, 19, 1–13.
  21. Kumar, S.; Pandey, A.K. Chemistry and biological activities of flavonoids: An overview. Sci. World J. 2013, 2013, 162750.
  22. Thilakarathna, S.H.; Rupasinghe, H.P. Flavonoid bioavailability and attempts for bioavailability enhancement. Nutrients 2013, 5, 3367–3387.
  23. De Pace, R.C.; Liu, X.; Sun, M.; Nie, S.; Zhang, J.; Cai, Q.; Gao, W.; Pan, X.; Fan, Z.; Wang, S. Anticancer activities of (−)-epigallocatechin-3-gallate encapsulated nanoliposomes in MCF7 breast cancer cells. J. Liposome Res. 2013, 23, 187–196.
  24. Davatgaran-Taghipour, Y.; Masoomzadeh, S.; Farzaei, M.H.; Bahramsoltani, R.; Karimi-Soureh, Z.; Rahimi, R.; Abdollahi, M. Polyphenol nanoformulations for cancer therapy: Experimental evidence and clinical perspective. Int. J. Nanomed. 2017, 12, 2689.
  25. Lee, T.J.; Kim, O.H.; Kim, Y.H.; Lim, J.H.; Kim, S.; Park, J.W.; Kwon, T.K. Quercetin arrests G2/M phase and induces caspase-dependent cell death in U937 cells. Cancer Lett. 2006, 240, 234–242.
  26. Lv, L.; Liu, C.; Chen, C.; Yu, X.; Chen, G.; Shi, Y.; Qin, F.; Ou, J.; Qiu, K.; Li, G. Quercetin and doxorubicin co-encapsulated biotin receptor-targeting nanoparticles for minimizing drug resistance in breast cancer. Oncotarget 2016, 7, 32184.
  27. Maetzel, D.; Denzel, S.; Mack, B.; Canis, M.; Went, P.; Benk, M.; Kieu, C.; Papior, P.; Baeuerle, P.A.; Munz, M.; et al. Nuclear signalling by tumour-associated antigen EpCAM. Nat. Cell Biol. 2009, 11, 162–171.
  28. Serra, D.; Parris, C.R.; Carper, E.; Homel, P.; Fleishman, S.B.; Harrison, L.B.; Chadha, M. Outcomes of guided imagery in patients receiving radiation therapy for breast cancer. Clin. J. Oncol. Nurs. 2012, 16, 617.
  29. Waks, A.G.; Winer, E.P. Breast cancer treatment: A review. JAMA 2019, 321, 288–300.
  30. Panche, A.N.; Diwan, A.D.; Chandra, S.R. Flavonoids: An overview. J. Nutr. Sci. 2016, 5, e47.
  31. Raina, R.; Hussain, A.; Sharma, R. Molecular insight into apoptosis mediated by flavones in cancer. World Acad. Sci. J. 2020, 2, 1.
  32. Xian, D.; Guo, M.; Xu, J.; Yang, Y.; Zhao, Y.; Zhong, J. Current evidence to support the therapeutic potential of flavonoids in oxidative stress-related dermatoses. Redox Rep. Commun. Free. Radic. Res. 2021, 26, 134–146.
  33. Wruck, C.J.; Claussen, M.; Fuhrmann, G.; Römer, L.; Schulz, A.; Pufe, T.; Wätzig, V.; Peipp, M.; Herdegen, T.; Götz, M.E. Luteolin protects rat PC 12 and C6 cells against MPP+ induced toxicity via an ERK dependent Keap-Nrf2-ARE pathway. Neuropsychiatr. Disord. Int. Approach 2007, 25, 57–67.
  34. Brusselmans, K.; Vrolix, R.; Verhoeven, G.; Swinnen, J.V. Induction of cancer cell apoptosis by flavonoids is associated with their ability to inhibit fatty acid synthase activity. J. Biol. Chem. 2005, 280, 5636–5645.
  35. Braakhuis, A.J.; Campion, P.; Bishop, K.S. Reducing breast cancer recurrence: The role of dietary polyphenolics. Nutrients 2016, 8, 547.
  36. Cui, L.; Liu, X.; Tian, Y.; Xie, C.; Li, Q.; Cui, H.; Sun, C. Flavonoids, flavonoid subclasses, and esophageal cancer risk: A meta-analysis of epidemiologic studies. Nutrients 2016, 8, 350.
  37. Sudan, S.; Rupasinghe, H.V. Quercetin-3-O-glucoside induces human DNA topoisomerase II inhibition, cell cycle arrest and apoptosis in hepatocellular carcinoma cells. Anticancer Res. 2014, 34, 1691–1699.
  38. Nath, S.; Mukherjee, P. MUC1: A multifaceted oncoprotein with a key role in cancer progression. Trends Mol. Med. 2014, 20, 332–342.
  39. Nikolaou, K.C.; Talianidis, I. Hepatic cancer stem cells may arise from adult ductal progenitors. MCO 2016, 3, e1021946.
  40. Noolu, B.; Gugulothu, R.; Bhat, M.; SYH Qadri, S.; Sudhakar Reddy, V.; Bhanuprakash Reddy, G.; Ismail, A. In vivo inhibition of proteasome activity and tumour growth by Murraya koenigii leaf extract in breast cancer xenografts and by its active flavonoids in breast cancer cells. Curr. Med. Chem. Anticancer Agents 2016, 16, 1605–1614.
  41. Imran, M.; Salehi, B.; Sharifi-Rad, J.; Aslam Gondal, T.; Saeed, F.; Imran, A.; Shahbaz, M.; Tsouh Fokou, P.V.; Umair Arshad, M.; Khan, H.; et al. Kaempferol: A key emphasis to its anticancer potential. Molecules 2019, 24, 2277.
  42. Iwashina, T. Flavonoid properties of five families newly incorporated into the order Caryophyllales. Bull. Natl. Mus. Nat. Sci. 2013, 39, 25–51.
  43. Barreca, D.; Gattuso, G.; Bellocco, E.; Calderaro, A.; Trombetta, D.; Smeriglio, A.; Laganà, G.; Daglia, M.; Meneghini, S.; Nabavi, S.M. Flavanones: Citrus phytochemical with health-promoting properties. BioFactors 2017, 43, 495–506.
  44. Akhtar Siddiqui, J.; Singh, A.; Chagtoo, M.; Singh, N.; Madhav Godbole, M.; Chakravarti, B. Phytochemicals for breast cancer therapy: Current status and future implications. Curr. Cancer Drug Targets 2015, 15, 116–135.
  45. Xiang, L.P.; Wang, A.; Ye, J.H.; Zheng, X.Q.; Polito, C.A.; Lu, J.L.; Li, Q.S.; Liang, Y.R. Suppressive effects of tea catechins on breast cancer. Nutrients 2016, 8, 458.
  46. Liang, Y.R.; Ye, Q.; Jin, J.; Liang, H.; Lu, J.L.; Du, Y.Y.; Dong, J.J. Chemical and instrumental assessment of green tea sensory preference. Int. J. Food Prop. 2008, 11, 258–272.
  47. Li, M.; Tse, L.A.; Chan, W.C.; Kwok, C.H.; Leung, S.L.; Wu, C.; Yu, W.C.; Yu, I.T.; Yu, C.H.; Wang, F.; et al. Evaluation of breast cancer risk associated with tea consumption by menopausal and estrogen receptor status among Chinese women in Hong Kong. Cancer Epidemiol. 2016, 40, 73–78.
  48. Suzuki, Y.; Tsubono, Y.; Nakaya, N.; Koizumi, Y.; Tsuji, I. Green tea and the risk of breast cancer: Pooled analysis of two prospective studies in Japan. Br. J. Cancer 2004, 90, 1361–1363.
  49. Zhang, M.; Holman, C.D.; Huang, J.P.; Xie, X. Green tea and the prevention of breast cancer: A case–control study in Southeast China. Carcinogenesis 2007, 28, 1074–1078.
  50. Yiannakopoulou, E.C. Effect of green tea catechins on breast carcinogenesis: A systematic review of in-vitro and in-vivo experimental studies. Eur. J. Cancer Prev. 2014, 23, 84–89.
  51. Alshatwi, A.A. Catechin hydrate suppresses MCF-7 proliferation through TP53/Caspase-mediated apoptosis. J. Exp. Clin. Cancer Res. 2010, 29, 1–9.
  52. Kucuk, O. Soy foods, isoflavones, and breast cancer. Cancer 2017, 123, 1901–1903.
  53. Messina, M. Soy foods, isoflavones, and the health of postmenopausal women. Am. J. Clin. Nutr. 2014, 100, 423S–430S.
  54. Messina, M. Soy and health update: Evaluation of the clinical and epidemiologic literature. Nutrients 2016, 8, 754.
  55. Badger, T.M.; Ronis, M.J.; Hakkak, R.; Rowlands, J.C.; Korourian, S. The health consequences of early soy consumption. J. Nutr. 2002, 132, 559S–565S.
  56. Křížová, L.; Dadáková, K.; Kašparovská, J.; Kašparovský, T. Isoflavones. Molecules 2019, 24, 1076.
  57. Lin, B.W.; Gong, C.C.; Song, H.F.; Cui, Y.Y. Effects of anthocyanins on the prevention and treatment of cancer. Br. J. Pharmacol. 2017, 174, 1226–1243.
  58. Diaconeasa, Z.; Știrbu, I.; Xiao, J.; Leopold, N.; Ayvaz, Z.; Danciu, C.; Ayvaz, H.; Stǎnilǎ, A.; Nistor, M.; Socaciu, C. Anthocyanins, Vibrant Color Pigments, and Their Role in Skin Cancer Prevention. Biomedicines 2020, 8, 336.
  59. Wang, L.S.; Stoner, G.D. Anthocyanins and their role in cancer prevention. Cancer Lett. 2008, 269, 281–290.
  60. Patra, J.K.; Das, G.; Fraceto, L.F.; Campos, E.V.; del Pilar Rodriguez-Torres, M.; Acosta-Torres, L.S.; Diaz-Torres, L.A.; Grillo, R.; Swamy, M.K.; Sharma, S.; et al. Nano based drug delivery systems: Recent developments and future prospects. J. Nanobiotechnol. 2018, 16, 1–33.
  61. Vaiserman, A.; Koliada, A.; Zayachkivska, A.; Lushchak, O. Nanodelivery of natural antioxidants: An anti-aging perspective. Front. Bioeng. Biotechnol. 2020, 7, 447.
  62. Dhupal, M.; Chowdhury, D. Phytochemical-Based Nanomedicine for Advanced Cancer Theranostics: Perspectives on Clinical Trials to Clinical Use. Int. J. Nanomed. 2020, 15, 9125.
  63. Sundar Dhilip Kumar, S.; Houreld, N.N.; Abrahamse, H. Therapeutic potential and recent advances of curcumin in the treatment of aging-associated diseases. Molecules 2018, 23, 835.
  64. Salehi, B.; Stojanović-Radić, Z.; Matejić, J.; Sharifi-Rad, M.; Kumar, N.V.; Martins, N.; Sharifi-Rad, J. The therapeutic potential of curcumin: A review of clinical trials. Eur. J. Med. Chem. 2019, 163, 527–545.
  65. Mohammad Hossein, K.; Amin, D.; Afsaneh, N.; Alireza, H.; Sima, H.; Fereidon, N.; Sepideh, K.; Maliheh, E.; Mehrdad, H.; Hossein, D. Analysis of the antiproliferative effects of curcumin and nanocurcumin in MDA-MB231 as a breast cancer cell line. Iran. J. Pharm. Res. 2016, 15, 231.
  66. Dobrzyńska, M.; Napierała, M.; Florek, E. Flavonoid Nanoparticles: A Promising Approach for Cancer Therapy. Biomolecules 2020, 10, 1268.
  67. Granja, A.; Pinheiro, M.; Reis, S. Epigallocatechin gallate nanodelivery systems for cancer therapy. Nutrients 2016, 8, 307.
  68. Frias, I.; Neves, A.R.; Pinheiro, M.; Reis, S. Design, development, and characterization of lipid nanocarriers-based epigallocatechin gallate delivery system for preventive and therapeutic supplementation. Drug Des. Devel. Ther. 2016, 10, 3519.
  69. Liao, B.; Ying, H.; Yu, C.; Fan, Z.; Zhang, W.; Shi, J.; Ying, H.; Ravichandran, N.; Xu, Y.; Yin, J.; et al. (−)-Epigallocatechin gallate (EGCG)-nanoerythrosomes as a transdermal delivery system for docetaxel to treat implanted human melanoma cell tumors in mice. Int. J. Pharm. 2016, 512, 22–31.
  70. Rajamani, S.; Radhakrishnan, A.; Sengodan, T.; Thangavelu, S. Augmented anticancer activity of naringenin-loaded TPGS polymeric nanosuspension for drug resistive MCF-7 human breast cancer cells. Drug Dev. Ind. Pharm. 2018, 44, 1752–1761.
  71. Noori, S.; Tavirani, M.R.; Deravi, N.; Rabbani, M.I.; Zarghi, A. Naringenin enhances the anti-cancer effect of cyclophosphamide against MDA-MB-231 breast cancer cells via targeting the STAT3 signaling pathway. Iran. J. Pharm. Res. IJPR 2020, 19, 122.
  72. Bhia, M.; Motallebi, M.; Abadi, B.; Zarepour, A.; Pereira-Silva, M.; Saremnejad, F.; Santos, A.C.; Zarrabi, A.; Melero, A.; Jafari, S.M.; et al. Naringenin nano-delivery systems and their therapeutic applications. Pharmaceutics 2021, 13, 291.
  73. Ramos, J.; Hatkevich, T.; Eanes, L.; Santos-Sanchez, I.; Patel, Y.M. Naringenin inhibits proliferation and survival of tamoxifen-resistant breast cancer cells. In Breast Cancer—From Biology to Medicine; IntechOpen: London, UK, 2017.
  74. Niazaand, F.; Razizadeh, M.; Khorsandi, L.; Abbaspour, M.; Mansouri, E.; Khodadadi, A. Effects of quercetin-loaded nanoparticles on MCF-7 human breast cancer cells. Medicina 2019, 55, 114.
  75. Kim, W.K.; Bang, M.H.; Kim, E.S.; Kang, N.E.; Jung, K.C.; Cho, H.J.; Park, J.H. Quercetin decreases the expression of ErbB2 and ErbB3 proteins in HT-29 human colon cancer cells. J. Nutr. Biochem. 2005, 16, 155–162.
  76. Ezzati, M.; Yousefi, B.; Velaei, K.; Safa, A. A review on anti-cancer properties of Quercetin in breast cancer. Life Sci. 2020, 248, 117463.
  77. Singh, R.; Kumari, P.; Kumar, S. Nanotechnology for enhanced bioactivity of bioactive phytomolecules. In Nutrient Delivery; Academic Press: Amsterdam, The Netherlands, 2017; pp. 413–456.
  78. Xiao, Q.; Zhu, W.; Feng, W.; Lee, S.S.; Leung, A.W.; Shen, J.; Gao, L.; Xu, C. A review of resveratrol as a potent chemoprotective and synergistic agent in cancer chemotherapy. Front. Pharmacol. 2019, 9, 1534.
  79. Shindikar, A.; Singh, A.; Nobre, M.; Kirolikar, S. Curcumin and resveratrol as promising natural remedies with nanomedicine approach for the effective treatment of triple negative breast cancer. J. Oncol. Res. 2016, 1–13.
  80. Mafuvadze, B.; Liang, Y.; Besch-Williford, C.; Zhang, X.; Hyder, S.M. Apigenin induces apoptosis and blocks growth of medroxyprogesterone acetate-dependent BT-474 xenograft tumors. Horm. Cancer 2012, 3, 160–171.
  81. Yan, X.; Qi, M.; Li, P.; Zhan, Y.; Shao, H. Apigenin in cancer therapy: Anti-cancer effects and mechanisms of action. Cell Biosci. 2017, 7, 50.
  82. Ding, S.M.; Zhang, Z.H.; Song, J.; Cheng, X.D.; Jiang, J.; Jia, X.B. Enhanced bioavailability of apigenin via preparation of a carbon nanopowder solid dispersion. Int. J. Nanomed. 2014, 9, 2327.
  83. Shankar, E.; Goel, A.; Gupta, K.; Gupta, S. Plant flavone apigenin: An emerging anticancer agent. Curr. Pharmacol. Rep. 2017, 3, 423–446.
  84. Liu, Y.; Xie, X.; Hou, Z.; Shen, J.; Shi, J.; Chen, H.; He, Y.; Wang, Z.; Feng, N. Functional oral nanoparticles for delivering silibinin and cryptotanshinone against breast cancer lung metastasis. J. Nanobiotechnol. 2020, 18, 83.
  85. Xu, P.; Yin, Q.; Shen, J.; Chen, L.; Yu, H.; Zhang, Z.; Li, Y. Synergistic inhibition of breast cancer metastasis by silibinin-loaded lipid nanoparticles containing TPGS. Int. J. Pharm. 2013, 454, 21–30.
  86. Ranganatha, S.; Shruthi, S.D.; Govindappa, M.; Ramachandra, Y.L. In silico studies of NF-κB protein as anti-cancer and anti-inflammatory target. J. Comput. Methods Mol. Des. 2013, 3, 26–33.
  87. Chen, W.F.; Huang, M.H.; Tzang, C.H.; Yang, M.; Wong, M.S. Inhibitory actions of genistein in human breast cancer (MCF-7) cells. Biochim. Biophys. Acta Mol. Basis Dis. 2003, 1638, 187–196.
  88. Pool, H.; Campos-Vega, R.; Herrera-Hernández, M.G.; García-Solis, P.; García-Gasca, T.; Sánchez, I.C.; Luna-Bárcenas, G.; Vergara-Castañeda, H. Development of genistein-PEGylated silica hybrid nanomaterials with enhanced antioxidant and antiproliferative properties on HT29 human colon cancer cells. Am. J. Transl. Res. 2018, 10, 2306.
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