Interleukin-4 induces senescence in human renal carcinoma cell lines through STAT6 and p38 MAPK

J Biol Chem. 2013 Oct 4;288(40):28743-54. doi: 10.1074/jbc.M113.499053. Epub 2013 Aug 9.

Abstract

Interleukin (IL)-4, originally identified as a lymphocyte growth factor, can directly inhibit growth of certain tumor cell types. We reported previously that IL-4 induced cell cycle arrest in G1 phase through an increase in p21(WAF1/CIP1) expression in human renal cell carcinoma (RCC) cell lines. In the present study, we investigated the underlying mechanism of IL-4-induced growth inhibition. In four of six human RCC cell lines, including Caki-1, A498, SNU482, and SNU228, IL-4 induced cellular senescence as demonstrated by enlarged and flattened morphology, increased granularity, and senescence-associated-β-galactosidase (SA-β-gal) staining. Signal tranducer and activator of transcription 6 (STAT6) and p38 MAPK were found to mediate IL-4-induced growth inhibition and cellular senescence. Both of these molecules were activated by 10 min after IL-4 treatment, and inhibition of their activity or expression prevented growth suppression and cellular senescence induced by IL-4. Inhibiting or silencing either STAT6 or p38 MAPK alone partially reduced the effect of IL-4, whereas inhibiting or silencing both molecules exerted an additive effect and almost completely abrogated the effect of IL-4. Thus STAT6 and p38 MAPK appeared to independently mediate IL-4-induced growth inhibition and cellular senescence. The p21(WAF1/CIP1) up-regulation that accompanied growth inhibition and cellular senescence by IL-4 was also attenuated additively when p38 MAPK and STAT6 were silenced. Taken together, these results show that IL-4 induces cellular senescence through independent signaling pathways involving STAT6 and p38 MAPK in some human RCC cell lines.

Keywords: IL-4; Interleukin; Renal Cell Carcinoma; Renal Physiology; STAT Transcription Factor; STAT6; Senescence; p21WAF1/CIP1; p38 MAPK.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Renal Cell / enzymology
  • Carcinoma, Renal Cell / genetics
  • Carcinoma, Renal Cell / pathology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cellular Senescence / drug effects*
  • Cellular Senescence / genetics
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Silencing / drug effects
  • Humans
  • Interleukin-4 / pharmacology*
  • Kidney Neoplasms / enzymology*
  • Kidney Neoplasms / genetics
  • Kidney Neoplasms / pathology*
  • STAT3 Transcription Factor / metabolism
  • STAT6 Transcription Factor / metabolism*
  • Up-Regulation / drug effects
  • Up-Regulation / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • IL4 protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • STAT6 Transcription Factor
  • STAT6 protein, human
  • Interleukin-4
  • p38 Mitogen-Activated Protein Kinases