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Autophagy regulation by p53

  • Maria Chiara Maiuri
  • , Lorenzo Galluzzi
  • , Eugenia Morselli
  • , Oliver Kepp
  • , Shoaib Ahmad Malik
  • , Guido Kroemer
  • INSERM; U848
  • Université Paris-Sud
  • Université Paris-Saclay

Research output: Contribution to journal › Review article › peer-review

472 Scopus citations

Abstract

Autophagy is an evolutionarily conserved catabolic pathway that is involved in numerous physiological processes and in multiple pathological conditions including cancer. Autophagy is regulated by an intricate network of signaling cascades that have not yet been entirely disentangled. Accumulating evidence indicates that p53, the best-characterized human tumor suppressor protein, can modulate autophagy in a dual fashion, depending on its subcellular localization. On the one hand, p53 functions as a nuclear transcription factor and transactivates proapoptotic, cell cycle-arresting and proautophagic genes. On the other hand, cytoplasmic p53 can operate at mitochondria to promote cell death and can repress autophagy via poorly characterized mechanisms. This review focuses on the recently discovered function of p53 as a master regulator of autophagy.

Original languageEnglish
Pages (from-to)181-185
Number of pages5
JournalCurrent Opinion in Cell Biology
Volume22
Issue number2
DOIs
StatePublished - Apr 2010

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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