Loss of Notch1 predisposes oro-esophageal epithelium to tumorigenesis

Exp Cell Res. 2018 Nov 15;372(2):129-140. doi: 10.1016/j.yexcr.2018.09.019. Epub 2018 Sep 25.


Notch signaling functions in diverse developmental and homeostatic processes, including stem cell self-renewal and cell fate determination. Notch1-inactivating mutations are frequently detected in skin and oro-esophageal cancers, suggesting a role for Notch1 as a tumor suppressor. Here, we clarify the contribution of Notch1 deficiency to oro-esophageal tumorigenesis using a physiological experimental model. Tongue and esophageal tumors induced in mice by 4-nitroquinoline-1-oxide (4-NQO) showed pathophysiological similarities to human tumors, including decreased Notch1 expression in the basal cells. We created mutant mice (N1cKO), in which the Notch1 gene was disrupted specifically in the squamous epithelium. The epithelium formed normally in N1cKO mice, and although multiple skin tumors were detected at 65 weeks, no tumors developed in the tongue and esophagus. However, 4-NQO-induced tumorigenesis assays revealed that tumor onset occurred earlier in N1cKO mice than in wild-type littermates, and the tumors arose preferentially from the Notch1-negative epithelium, indicating the tumor susceptibility of Notch1-deficient epithelium. Notch1 regulates the expression of TERT, and age-related telomere erosion was more rapid in Notch1-deficient basal cells. Our results indicated that although Notch1 deficiency had little effect on squamous epithelium formation, it predisposed the affected epithelium to tumor development, at least in part through accelerated telomere erosion.

Keywords: CRISPR/Cas9; Esophageal cancer; Head and neck cancer; Notch1; TERT; Telomere.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Nitroquinoline-1-oxide / toxicity
  • Animals
  • Carcinogenesis / genetics*
  • Disease Models, Animal
  • Epithelium / metabolism
  • Epithelium / pathology
  • Esophageal Neoplasms / chemically induced
  • Esophageal Neoplasms / genetics*
  • Esophageal Neoplasms / pathology
  • Esophagus / metabolism
  • Esophagus / pathology
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Mice
  • Mice, Knockout
  • Receptor, Notch1 / genetics*
  • Telomerase / genetics
  • Telomere / genetics
  • Tongue Neoplasms / chemically induced
  • Tongue Neoplasms / genetics*
  • Tongue Neoplasms / pathology


  • Notch1 protein, mouse
  • Receptor, Notch1
  • 4-Nitroquinoline-1-oxide
  • Telomerase
  • Tert protein, mouse