Frontiers in Cell and Developmental Biology (Mar 2022)

Myc Supports Self-Renewal of Basal Cells in the Esophageal Epithelium

  • Tomoaki Hishida,
  • Tomoaki Hishida,
  • Eric Vazquez-Ferrer,
  • Yuriko Hishida-Nozaki,
  • Yuto Takemoto,
  • Fumiyuki Hatanaka,
  • Kei Yoshida,
  • Javier Prieto,
  • Sanjeeb Kumar Sahu,
  • Yuta Takahashi,
  • Pradeep Reddy,
  • David D. O’Keefe,
  • Concepcion Rodriguez Esteban,
  • Paul S. Knoepfler,
  • Estrella Nuñez Delicado,
  • Antoni Castells,
  • Josep M. Campistol,
  • Ryuji Kato,
  • Hiroshi Nakagawa,
  • Hiroshi Nakagawa,
  • Juan Carlos Izpisua Belmonte

DOI
https://doi.org/10.3389/fcell.2022.786031
Journal volume & issue
Vol. 10

Abstract

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It is widely believed that cellular senescence plays a critical role in both aging and cancer, and that senescence is a fundamental, permanent growth arrest that somatic cells cannot avoid. Here we show that Myc plays an important role in self-renewal of esophageal epithelial cells, contributing to their resistance to cellular senescence. Myc is homogeneously expressed in basal cells of the esophageal epithelium and Myc positively regulates their self-renewal by maintaining their undifferentiated state. Indeed, Myc knockout induced a loss of the undifferentiated state of esophageal epithelial cells resulting in cellular senescence while forced MYC expression promoted oncogenic cell proliferation. A superoxide scavenger counteracted Myc knockout-induced senescence, therefore suggesting that a mitochondrial superoxide takes part in inducing senescence. Taken together, these analyses reveal extremely low levels of cellular senescence and senescence-associated phenotypes in the esophageal epithelium, as well as a critical role for Myc in self-renewal of basal cells in this organ. This provides new avenues for studying and understanding the links between stemness and resistance to cellular senescence.

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