Abstract

Background: The expression and function of the MYC family of oncoproteins are tightly regulated in normal cells, but it becomes deregulated in up to 70% of human cancers through a variety of mechanisms, functioning as a master modulator of the cancer transcriptome. Despite the broad therapeutic utility anticipated for a clinical MYC inhibitor, MYC remains considered undruggable, and so far, no direct MYC inhibitor has been approved for clinical use.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call