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Molecular oncology

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222:, have been found to reduce the ability of T cells to multiply within the body. In order to optimize the efficacy of CAR-T gene therapy, these checkpoint inhibitors can be blocked to stimulate a robust anti-tumor immune response, spearheaded by the CAR-T cells. There are various known inhibitory receptors on the CAR-T cell; through manipulation of these receptors and the molecules that bind them, expression of the CAR-T cell can be amplified. 1393: 1423: 1433: 1413: 1403: 246:
There is room for improvement with this gene therapy approach. Firstly, the antigens of interest expressed on the cancer cells may sometimes be expressed on regular body cells, too. This means the body's T cells will attack its own healthy cells instead of the cancer cells when the antigen is lacking
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and other pathways involved in cellular and genomic integrity. By halting the cell cycle, these genes ensure that genetically damaged cells are not passing on that damage to daughter cells. The cell cycle may be paused and if the damage is severe enough, the p53 and PTEN gene pathways may signal for
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of these cancerous cells that are functioning with severely damaged genomes. Cancer cells do not behave like normal cells, so the methods for ridding the body of these cells are more complicated. Manipulation of the pathways controlled by certain genes and their regulators are a large branch of
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drugs and other cancer treatments, or imaging scans. Scientists use a range of techniques to validate the role of the novel candidate genes in the development of cancer. The ultimate aim is to translate these findings into improved treatment options for cancer patients.
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to improve the efficacy of the immunotherapy method. Cytokines are messenger molecules that can act on themselves, nearby cells, or distant cells. The signal pathways of these cytokines can be used to enhance CAR-T anti-tumor characteristics. For example,
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specificity with just the cancer cell. A possible solution to this problem is to include two different antigen receptors on the CAR-T cells to make them even more specific. The second issue with the CAR-T immunotherapy approach is that it can cause
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Räty, J. K.; Pikkarainen, J. T.; Wirth, T.; Ylä-Herttuala, S. (January 2008). "Gene therapy: the first approved gene-based medicines, molecular mechanisms and clinical indications".
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because their pathways oversee the repair of cells that may replicate out of control with damaged genetic material, eventually leading to cancer growth if not kept in check.
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for various immune system cells, including T cells. In regards to gene therapy, IL2 can be used to increase replication and dispersing of CAR-T cells throughout the body.
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Gershovich, PM; Karabelskii, AV (2019). "The Role of Checkpoint Inhibitors and Cytokines in Adoptive Cell Based Cancer Immunotherapy with Genetically Modified T Cells".
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is a targeted approach to cancer therapy where actual immune cells of the patient and their genes are manipulated to produce an anti-tumor response. The body's own
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is used to attack the tumor cells, therefore the immune system can naturally attack the specific cancer cells again to in the future if necessary. Many types of
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to express a chimeric antigen receptor. This receptor, now on millions of the patient's T cells, recognizes cancerous cells that express specific
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Molecular oncology has identified genes that are involved in the development of cancer. The research combined diverse techniques ranging from
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Tazawa, Hiroshi; Kagawa, Shunsuke; Fujiwara, Toshiyoshi (November 2013). "Advances in adenovirus-mediated p53 cancer gene therapy".
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Luongo, Francesca; Colonna, Francesca; CalapĂ , Federica; Vitale, Sara; Fiori, Micol E.; De Maria, Ruggero (2019-07-30).
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In the past few decades, gene therapy has emerged as a targeted way to treat cancer. Gene therapy introduces foreign
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There are many different genes being researched for possible cancer therapies. Among the most studied are the
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Helmy, KY; Patel, SA (October 2013). "Cancer immunotherapy: accomplishments to date and future promise".
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factors are released by the immune system and can cause unpleasant side effects for the patient like
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therapies, and various manipulations of host immune cells to target and kill cancer cells.
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the death of the damaged cells. Both the p53 and PTEN genes are classified as
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molecules are some such cellular manipulations to target cancer cells.
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in these genes are seen in more than half of human cancers.
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Combining CAR-T with checkpoint inhibitors, cytokines
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that refers to the investigation of the chemistry of
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These genes are major regulators of the 1264:Bachelor of Medicine, Bachelor of Surgery 457: 439: 275:to diseased cells in order to change the 1473:Interdisciplinary subfields of medicine 306: 498:Sun, Weiming; Shi (January 26, 2019). 225:CAR-T cells can also be combined with 33:medical specialty at the interface of 574: 572: 570: 568: 566: 564: 562: 560: 7: 1402: 1163:Physical medicine and rehabilitation 493: 491: 489: 487: 485: 483: 481: 479: 477: 330:Expert Opinion on Biological Therapy 323: 321: 1412: 234:(IL2) is a cytokine that acts as a 16:Interdisciplinary medical specialty 1299:Medical Scientist Training Program 14: 1431: 1421: 1411: 1401: 1392: 1391: 188:Chimeric antigen receptor T cell 183:Chimeric antigen receptor T Cell 1432: 1289:Doctor of Osteopathic Medicine 723:Oral and maxillofacial surgery 381:Current Molecular Pharmacology 55:molecularly targeted therapies 1: 142:Molecular oncolytic therapies 19:For the medical journal, see 1269:Bachelor of Medical Sciences 1036:Neurosurgical anesthesiology 342:10.1517/14712598.2013.845662 251:. This is when an excess of 21:Molecular Oncology (journal) 518:– via Web of Science. 393:10.2174/1874467210801010013 1489: 18: 1387: 593:10.1134/S0006297919070022 249:cytokine release syndrome 242:Issues with CAR-T therapy 1223:Transplantation medicine 1114:Clinical neurophysiology 1031:Obstetric anesthesiology 951:Interventional radiology 711:Digestive system surgery 1094:Intensive care medicine 1068:Mass gathering medicine 913:Maternal–fetal medicine 441:10.3390/cancers11081076 686:Cardiothoracic surgery 218:, specifically immune 1337:Personalized medicine 1196:Reproductive medicine 1121:Occupational medicine 1075:Evolutionary medicine 581:Biochemistry (Moscow) 220:checkpoint inhibitors 196:checkpoint inhibitors 71:computational biology 1357:Traditional medicine 1317:Alternative medicine 1184:Addiction psychiatry 998:Transfusion medicine 993:Medical microbiology 908:Gynecologic oncology 760:Reproductive surgery 531:Therapeutic Delivery 1463:Medicinal chemistry 1379:History of medicine 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Index

Molecular Oncology (journal)
interdisciplinary
medicinal chemistry
oncology
cancer
tumors
molecular
molecularly targeted therapies
genomics
computational biology
tumour
imaging
in vitro
in vivo
phenotypes
proteins
genes
targets
chemotherapy
p53 gene
PTEN gene
cell cycle
tumor suppressors
Mutations
gene therapy
immune system
immunotherapies
bone marrow
antibody
Cellular receptors

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