CRISPR/Cas mediated epigenome editing for cancer therapy

dc.contributor.authorChitkara, Deepak
dc.date.accessioned2024-01-04T09:17:48Z
dc.date.available2024-01-04T09:17:48Z
dc.date.issued2022-08
dc.description.abstractThe understanding of the relationship between epigenetic alterations, their effects on gene expression and the knowledge that these epigenetic alterations are reversible, have opened up new therapeutic pathways for treating various diseases, including cancer. This has led the research for a better understanding of the mechanism and pathways of carcinogenesis and provided the opportunity to develop the therapeutic approaches by targeting such pathways. Epi-drugs, DNA methyl transferase (DNMT) inhibitors and histone deacetylase (HDAC) inhibitors are the best examples of epigenetic therapies with clinical applicability. Moreover, precise genome editing technologies such as CRISPR/Cas has proven their efficacy in epigenome editing, including the alteration of epigenetic markers, such as DNA methylation or histone modification. The main disadvantage with DNA gene editing technologies is off-target DNA sequence alteration, which is not an issue with epigenetic editing. It is known that cancer is linked with epigenetic alteration, and thus CRISPR/Cas system shows potential for cancer therapy via epigenome editing. This review outlines the epigenetic therapeutic approach for cancer therapy using CRISPR/Cas, from the basic understanding of cancer epigenetics to potential applications of CRISPR/Cas in treating cancer.en_US
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1044579X20302789
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13659
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPharmacyen_US
dc.subjectEpigeneticsen_US
dc.subjectGenome editingen_US
dc.subjectEpigenome editingen_US
dc.subjectCRISPR/Cas9en_US
dc.subjectCRISPR/dCas9en_US
dc.titleCRISPR/Cas mediated epigenome editing for cancer therapyen_US
dc.typeArticleen_US

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