c-Met as a new marker of cellular senescence

Aging (Albany NY). 2019 May 13;11(9):2889-2897. doi: 10.18632/aging.101961.

Abstract

Here, we reported for the first time an increased expression of c-Met protein in primary cultures of human dermal and pulmonary fibroblasts of late passages. This suggests that c-Met could serve as an early marker of cellular senescence (CS). The levels of c-Met-related signaling proteins phospho-Akt and Stat3 were also increased in (pre)senescent fibroblasts. Considering the anti-apoptotic activity of Akt and the involvement of Stat3 in mediating the effects of proinflammatory cytokines, the findings of this study indicate that c-Met could contribute through its downstream targets or partners to at least two major phenotypical features of CS - resistance to apoptosis and senescence-associated secretory phenotype.

Keywords: Akt; Stat3; c-Met; cellular senescence; human dermal and pulmonary fibroblasts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers
  • Cells, Cultured
  • Cellular Senescence / physiology*
  • Fibroblasts / metabolism*
  • Gene Expression Regulation
  • Humans
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / physiology
  • Proto-Oncogene Proteins c-met* / chemistry
  • Proto-Oncogene Proteins c-met* / metabolism
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism

Substances

  • Biomarkers
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Proto-Oncogene Proteins c-met
  • Proto-Oncogene Proteins c-akt