Targeting p53 as a promising therapeutic option for cancer by re-activating the wt or mutant p53’s tumor suppression

Author:

Węsierska-Gądek Józefa1

Affiliation:

1. Cell Cycle Regulation Group, Department of Medicine, Institute of Cancer Research, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria

Abstract

p53 protein, a product of the TP53 tumor suppressor gene, controls the cellular genome’s integrity and is an important regulator of cell cycling, proliferation, apoptosis and metabolism. Mutations of TP53 or inactivation of its gene product are among the first events initiating malignant transformation. The consequent loss of control over the cell cycle, resulting in accelerated cell proliferation and facilitating metabolic reprogramming, gives the initiated (premalignant) cells numerous advantages over healthy cells. Interestingly, p53 status is not only an important marker in cancer diagnosis; it has also become a promising target of personalized therapy. Depending on the TP53 status different therapeutic options have been developed. (Re)-activation of p53 functionality in cancer cells offers promising new alternatives to existing oncological therapies.

Publisher

Future Science Ltd

Subject

Drug Discovery,Pharmacology,Molecular Medicine

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