High intensity ras signaling induces premature senescence by activating p38 pathway in primary human fibroblasts

J Biol Chem. 2004 Jan 9;279(2):1050-9. doi: 10.1074/jbc.M308644200. Epub 2003 Oct 29.

Abstract

Although oncogenic ras plays a pivotal role in neoplastic transformation, it triggers an anti-oncogenic defense mechanism known as premature senescence in normal cells. In this study, we investigated the induction of cellular responses by different expression levels of oncogenic ras in primary human fibroblasts. We found that a moderate, severalfold increase in ras expression promoted cell growth. Further elevation of ras expression initially enhanced proliferation but eventually induced p16INK4A expression and senescence. The induction of these opposing cellular responses by ras signals of different intensity was achieved through differential activation of the MAPK pathways that mediated these responses. Whereas moderate ras activities only stimulated the mitogenic MEK-ERK pathway, high intensity ras signals induced MEK and ERK to higher levels, leading to stimulation of the MKK3/6-p38 pathway, which had been shown previously to act downstream of Ras-MEK to trigger the senescence response. Thus, these studies have revealed a mechanism for the differential effects of ras on cell proliferation. Furthermore, moderate ras activity mediated transformation in cooperation with E6E7 and hTERT, suggesting that a moderate intensity ras signal can provide sufficient oncogenic activities for tumorigenesis. This result also implies that the ability of ras to promote proliferation and oncogenic transformation can be uncoupled with that to induce senescence in cell culture and that the development of tumors with relatively low ras activities may not need to acquire genetic alterations that bypass premature senescence.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Blotting, Southern
  • Cell Division
  • Cell Line
  • Cell Transformation, Neoplastic
  • Cells, Cultured
  • Cellular Senescence
  • Cyclin-Dependent Kinase Inhibitor p16 / metabolism
  • DNA-Binding Proteins
  • Dose-Response Relationship, Drug
  • Doxycycline / pharmacology
  • Enzyme Activation
  • Fibroblasts / metabolism*
  • Genetic Vectors
  • Green Fluorescent Proteins
  • Humans
  • Karyotyping
  • Luminescent Proteins / metabolism
  • Male
  • Mitogen-Activated Protein Kinases / metabolism*
  • Models, Biological
  • Retroviridae / genetics
  • Signal Transduction
  • Telomerase / metabolism
  • Time Factors
  • p38 Mitogen-Activated Protein Kinases
  • ras Proteins / metabolism*

Substances

  • Cyclin-Dependent Kinase Inhibitor p16
  • DNA-Binding Proteins
  • Luminescent Proteins
  • Green Fluorescent Proteins
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Telomerase
  • ras Proteins
  • Doxycycline