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Topic Review
CRISPR/Cas-Based Cell Therapy for Type 1 Diabetes
Type 1 diabetes mellitus (T1D) is an autoimmune disease caused by the destruction of insulin-producing β-cells in the pancreas by cytotoxic T-cells. To date, there are no drugs that can prevent the development of T1D. Insulin replacement therapy is the standard care for patients with T1D. This treatment is life-saving, but is expensive, can lead to acute and long-term complications, and results in reduced overall life expectancy. This has stimulated the research and development of alternative treatments for T1D. In this research, potential therapies for T1D are considered using cellular regenerative medicine approaches with a focus on CRISPR/Cas-engineered cellular products. However, CRISPR/Cas as a genome editing tool has several drawbacks that should be considered for safe and efficient cell engineering. In addition, cellular engineering approaches themselves pose a hidden threat. The purpose of this research is to critically discuss novel strategies for the treatment of T1D using genome editing technology. 
  • 292
  • 26 Dec 2023
Topic Review
Cell Immortalization
Somatic human cells can divide a finite number of times, a phenomenon known as the Hayflick limit. It is based on the progressive erosion of the telomeric ends each time the cell completes a replicative cycle. Given this problem, researchers need cell lines that do not enter the senescence phase after a certain number of divisions. In this way, more lasting studies can be carried out over time and avoid the tedious work involved in performing cell passes to fresh media. However, some cells have a high replicative potential, such as embryonic stem cells and cancer cells. To accomplish this, these cells express the enzyme telomerase or activate the mechanisms of alternative telomere elongation, which favors the maintenance of the length of their stable telomeres. Researchers have been able to develop cell immortalization technology by studying the cellular and molecular bases of both mechanisms and the genes involved in the control of the cell cycle. Through it, cells with infinite replicative capacity are obtained. To obtain them, viral oncogenes/oncoproteins, myc genes, ectopic expression of telomerase, and the manipulation of genes that regulate the cell cycle, such as p53 and Rb, have been used.
  • 291
  • 05 May 2023
Topic Review
Immunopathogenesis of COVID-19
The coronavirus disease 2019 (COVID-19) is caused by the infection of the novel highly contagious severe acute respiratory syndrome virus (SARS-CoV-2), viral infection can cause acute respiratory distress syndrome (ARDS) and, in severe cases, can even be lethal. Behind the inflammatory process lies the so-called cytokine storm (CS), which activates various inflammatory cytokines that damage numerous organ tissues.
  • 291
  • 26 Jun 2023
Topic Review
Preclinical and Clinical Endeavors Targeting Mitochondria
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterized by the progressive loss of motor neurons, for which current treatment options are limited. Recent studies have shed light on the role of mitochondria in ALS pathogenesis, making them an attractive therapeutic intervention target.
  • 291
  • 26 Feb 2024
Topic Review
Epoetin Alfa
Epoetin alfa is a human erythropoietin produced in cell culture using recombinant DNA technology. Authorised by the European Medicines Agency on 28 August 2007, it stimulates erythropoiesis (increasing red blood cell levels) and is used to treat anemia, commonly associated with chronic kidney failure and cancer chemotherapy. Epoetin is manufactured and marketed by Amgen under the brand name Epogen. Johnson & Johnson subsidiary Janssen Biotech (formerly Ortho Biotech Products, LP), sells the same drug under the name Procrit, pursuant to a product license agreement. The average cost per patient in the U.S. was $8,447 in 2009. Darbepoetin alfa (rINN) /dɑːrbəˈpɔɪtɪn/ is a glycosylation analog of erythropoietin containing two additional N-linked carbohydrate chains, also manufactured and marketed by Amgen, with a brand name of Aranesp. The Food and Drug Administration (FDA) warnings and safety precautions for Procrit, Epogen and Aranesp are identical. For several years, epoetin alfa has accounted for the single greatest drug expenditure paid by the U.S. Medicare system; in 2010, the program paid $2 billion for the drug. Raising hemoglobin levels has been found in some studies to be associated with higher risks of thrombotic events, strokes and death. It is on the World Health Organization's List of Essential Medicines.
  • 290
  • 01 Nov 2022
Topic Review
Perspectives of Metabolic Syndrome-Related Organoids
Organoids are spontaneously formed multicellular structures that provide a reliable model for studying early development and certain diseases. MetS is a systemic disease that affects multiple organs and tissues throughout the human body. A single organoid is not a good model for studying metabolic syndrome, as it lacks the organ-to-organ and system-to-system interactions necessary to study the disease. Secondly, the current immaturity of organoids and the inability to produce them on a large scale and in a standardized manner have created significant limitations for the study of various diseases, especially systemic diseases such as Mets. However, the combination of organoids with other technologies is expected to break the metabolic syndrome research bottleneck. 
  • 290
  • 22 May 2023
Topic Review
Lipid Droplets in Yeast during Stress and Aging
The baker’s yeast Saccharomyces cerevisiae is a valuable tool for aging research, as many aging- and disease-associated pathways such as DNA repair mechanisms, lipostasis, proteostasis, oxidative stress responses, regulated cell death, nutrient signaling, autophagy, and regulation of the cell cycle are evolutionarily conserved to a high degree. Lipid droplets (LDs) are evolutionary conserved structures that were mentioned for the first time by Van Leeuwenhoek in 1674, but their reassessment as autonomous organelles with important key roles in lipid and energy metabolism occurred many years later. LDs originate from the endoplasmic reticulum (ER). In the first step, neutral lipids are synthesized at the ER and are redirected into the bilayer, leading to an aggregation of the highly motile lipids. Emerging evidence suggests that LDs also fulfil impotant functions during aging and in protein homeostasis.
  • 289
  • 12 Oct 2023
Topic Review
Neoangiogenesis and Extracellular Matrix of HNSCC
Head and neck squamous cell cancer (HNSCC) is one of the ten most common malignant neoplasms, characterized by an aggressive course, high recurrence rate, poor response to treatment, and low survival rate. This creates the need for a deeper understanding of the mechanisms of the pathogenesis of this cancer. The tumor microenvironment (TME) of HNSCC consists of stromal and immune cells, blood and lymphatic vessels, and extracellular matrix. It is known that HNSCC is characterized by complex relationships between cancer cells and TME components. TME components and their dynamic interactions with cancer cells enhance tumor adaptation to the environment, which provides the highly aggressive potential of HNSCC and resistance to antitumor therapy.
  • 289
  • 30 Nov 2023
Topic Review
Microbiomics in Carcinogenesis
The microbiota–gut–brain axis consists of the brain, glands, gut, immune cells, and gastrointestinal microbiota. Both the central and enteric nervous systems regulate the communication between the gastrointestinal tract and the brain and apart from the nervous system, it is also regulated through hormones and immunological signalling. Multiple lines of evidence confirm the existence of the gut–brain axis.
  • 288
  • 27 Oct 2021
Topic Review
Protein Quality Control Systems in SARS-CoV-2 Infection
SARS-CoV-2’s structure and mechanism of infection have been well characterized. The virus comprises a lipid envelope studded with spike (S) proteins. These spikes facilitate viral entry into host cells by binding to angiotensin-converting enzyme 2 (ACE2) receptors on the cell surface. Following attachment, the virus enters the cell by endocytosis. Its genetic material consists of a single-stranded RNA molecule, which encodes structural proteins, non-structural proteins (NSP), and accessory proteins. Once inside, the viral RNA is translated into proteins, including those for replication and the formation of new virus particles.
  • 287
  • 24 Jan 2024
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