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Journal ArticleDOI

Oncogenomics and CYP450 Implications in Personalized Cancer Therapy

G.K. Udayaraja, +1 more
- 31 Jul 2020 - 
- Vol. 17, Iss: 2, pp 104-113
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TLDR
This review outlines the roles of oncogenes, the importance of cytochrome P450 (CYP450) in cancer susceptibility, and its impact on drug metabolism, proposing combined approaches to achieve precision therapy.
Abstract
\n\nThe Human Genome Project has unleashed the power of genomics\nin clinical practice as a choice of individualized therapy, particularly in cancer\ntreatment. Pharmacogenomics is an interdisciplinary field of genomics that deals with\ndrug response, based on individual genetic makeup.\n\n\n\nThe main genetic events associated with carcinogenesis activate oncogenes or\ninactivate tumor-suppressor genes. Therefore, drugs should be specific to inactivate or\nregulate these mutant genes and their protein products for effective cancer treatment. In\nthis review, we summarize how polymedication decisions in cancer treatments based on\nthe evaluation of cytochrome P450 (CYP450) polymorphisms are applied for pharmacogenetic\nassessment of anticancer therapy outcomes.\n\n\n\nHowever, multiple genetic events linked, inactivating a single mutant gene product,\nmay be insufficient to inhibit tumor progress. Thus, genomics and pharmacogenetics\ndirectly influence a patient’s response and aid in guiding clinicians to select the safest and\nmost effective combination of medications for a cancer patient from the initial prescription.\n\n\n\nThis review outlines the roles of oncogenes, the importance of cytochrome\nP450 (CYP450) in cancer susceptibility, and its impact on drug metabolism, proposing\ncombined approaches to achieve precision therapy.\n

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References
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Journal ArticleDOI

Cytochrome P450 enzymes in drug metabolism: Regulation of gene expression, enzyme activities, and impact of genetic variation

TL;DR: Recent progress on drug metabolism activity profiles, interindividual variability and regulation of expression, and the functional and clinical impact of genetic variation in drug metabolizing P450s are reviewed.
Journal ArticleDOI

Role of Aryl Hydrocarbon Receptor-mediated Induction of the CYP1 Enzymes in Environmental Toxicity and Cancer

TL;DR: Differences in AHR affinity between inbred mouse strains reflect variations in CYP1 inducibility and clearly have been shown to be associated with differences in risk of toxicity or cancer caused by PAHs and arylamines.
Journal ArticleDOI

Comparison of cytochrome P450 (CYP) genes from the mouse and human genomes, including nomenclature recommendations for genes, pseudogenes and alternative-splice variants.

TL;DR: The cytochrome P450 (CYP) gene superfamily is summarized and complete identification of all pseudogene sequences is likely to be clinically important, because some of these highly similar exons can interfere with PCR-based genotyping assays.
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