Biomedicines (Jun 2022)

P63 and P73 Activation in Cancers with p53 Mutation

  • Bi-He Cai,
  • Yun-Chien Hsu,
  • Fang-Yu Yeh,
  • Yu-Rou Lin,
  • Rui-Yu Lu,
  • Si-Jie Yu,
  • Jei-Fu Shaw,
  • Ming-Han Wu,
  • Yi-Zhen Tsai,
  • Ying-Chen Lin,
  • Zhi-Yu Bai,
  • Yu-Chen Shih,
  • Yi-Chiang Hsu,
  • Ruo-Yu Liao,
  • Wei-Hsin Kuo,
  • Chao-Tien Hsu,
  • Ching-Feng Lien,
  • Chia-Chi Chen

DOI
https://doi.org/10.3390/biomedicines10071490
Journal volume & issue
Vol. 10, no. 7
p. 1490

Abstract

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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.

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