Gene transactivation and transrepression in myc-driven cancers

23Citations
Citations of this article
40Readers
Mendeley users who have this article in their library.

Abstract

MYC is a proto-oncogene regulating a large number of genes involved in a plethora of cellular functions. Its deregulation results in activation of MYC gene expression and/or an increase in MYC protein stability. MYC overexpression is a hallmark of malignant growth, inducing self-renewal of stem cells and blocking senescence and cell differentiation. This review summarizes the latest advances in our understanding of MYC-mediated molecular mechanisms responsible for its oncogenic activity. Several recent findings indicate that MYC is a regulator of cancer genome and epigenome: MYC modulates expression of target genes in a site-specific manner, by recruiting chromatin remodeling co-factors at promoter regions, and at genome-wide level, by regulating the expression of several epigenetic modifiers that alter the entire chromatin structure. We also discuss novel emerging therapeutic strategies based on both direct modulation of MYC and its epigenetic cofactors.

Cite

CITATION STYLE

APA

Scafuro, M., Capasso, L., Carafa, V., Altucci, L., & Nebbioso, A. (2021, April 1). Gene transactivation and transrepression in myc-driven cancers. International Journal of Molecular Sciences. MDPI AG. https://doi.org/10.3390/ijms22073458

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free