P63 and P73 Activation in Cancers with p53 Mutation

Author:

Cai Bi-HeORCID,Hsu Yun-Chien,Yeh Fang-Yu,Lin Yu-Rou,Lu Rui-Yu,Yu Si-Jie,Shaw Jei-FuORCID,Wu Ming-Han,Tsai Yi-Zhen,Lin Ying-Chen,Bai Zhi-Yu,Shih Yu-Chen,Hsu Yi-ChiangORCID,Liao Ruo-Yu,Kuo Wei-Hsin,Hsu Chao-Tien,Lien Ching-FengORCID,Chen Chia-ChiORCID

Abstract

The members of the p53 family comprise p53, p63, and p73, and full-length isoforms of the p53 family have a tumor suppressor function. However, p53, but not p63 or p73, has a high mutation rate in cancers causing it to lose its tumor suppressor function. The top and second-most prevalent p53 mutations are missense and nonsense mutations, respectively. In this review, we discuss possible drug therapies for nonsense mutation and a missense mutation in p53. p63 and p73 activators may be able to replace mutant p53 and act as anti-cancer drugs. Herein, these p63 and p73 activators are summarized and how to improve these activator responses, particularly focusing on p53 gain-of-function mutants, is discussed.

Funder

I-Shou University and E-Da Medical Consortium Legal Person Research Cooperation Project

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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