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CRISPR/Cas mediated epigenome editing for cancer therapy

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dc.contributor.author Chitkara, Deepak
dc.date.accessioned 2024-01-04T09:17:48Z
dc.date.available 2024-01-04T09:17:48Z
dc.date.issued 2022-08
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/S1044579X20302789
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13659
dc.description.abstract The 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.language.iso en en_US
dc.publisher Elsevier en_US
dc.subject Pharmacy en_US
dc.subject Epigenetics en_US
dc.subject Genome editing en_US
dc.subject Epigenome editing en_US
dc.subject CRISPR/Cas9 en_US
dc.subject CRISPR/dCas9 en_US
dc.title CRISPR/Cas mediated epigenome editing for cancer therapy en_US
dc.type Article en_US


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