Cell Death and Disease (May 2023)

KLF5 and p53 comprise an incoherent feed-forward loop directing cell-fate decisions following stress

  • Yizeng Yang,
  • Dharmendra Bhargava,
  • Xiao Chen,
  • Taicheng Zhou,
  • Gizem Dursuk,
  • Wenpeng Jiang,
  • Jinshen Wang,
  • Zhen Zong,
  • Sharyn I. Katz,
  • Gwen A. Lomberk,
  • Raul A. Urrutia,
  • Jonathan P. Katz

DOI
https://doi.org/10.1038/s41419-023-05731-1
Journal volume & issue
Vol. 14, no. 5
pp. 1 – 10

Abstract

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Abstract In response to stress, cells make a critical decision to arrest or undergo apoptosis, mediated in large part by the tumor suppressor p53. Yet the mechanisms of these cell fate decisions remain largely unknown, particularly in normal cells. Here, we define an incoherent feed-forward loop in non-transformed human squamous epithelial cells involving p53 and the zinc-finger transcription factor KLF5 that dictates responses to differing levels of cellular stress from UV irradiation or oxidative stress. In normal unstressed human squamous epithelial cells, KLF5 complexes with SIN3A and HDAC2 repress TP53, allowing cells to proliferate. With moderate stress, this complex is disrupted, and TP53 is induced; KLF5 then acts as a molecular switch for p53 function by transactivating AKT1 and AKT3, which direct cells toward survival. By contrast, severe stress results in KLF5 loss, such that AKT1 and AKT3 are not induced, and cells preferentially undergo apoptosis. Thus, in human squamous epithelial cells, KLF5 gates the response to UV or oxidative stress to determine the p53 output of growth arrest or apoptosis.