Activated H-Ras regulates hematopoietic cell survival by modulating Survivin

Biochem Biophys Res Commun. 2004 Oct 15;323(2):636-44. doi: 10.1016/j.bbrc.2004.08.149.

Abstract

Survivin expression and Ras activation are regulated by hematopoietic growth factors. We investigated whether activated Ras could circumvent growth factor-regulated Survivin expression and if a Ras/Survivin axis mediates growth factor independent survival and proliferation in hematopoietic cells. Survivin expression is up-regulated by IL-3 in Ba/F3 and CD34+ cells and inhibited by the Ras inhibitor, farnesylthiosalicylic acid. Over-expression of constitutively activated H-Ras (CA-Ras) in Ba/F3 cells blocked down-modulation of Survivin expression, G0/G1 arrest, and apoptosis induced by IL-3 withdrawal, while dominant-negative (DN) H-Ras down-regulated Survivin. Survivin disruption by DN T34A Survivin blocked CA-Ras-induced IL-3-independent cell survival and proliferation; however, it did not affect CA-Ras-mediated enhancement of S-phase, indicating that the anti-apoptotic activity of CA-Ras is Survivin dependent while its S-phase enhancing effect is not. These results indicate that CA-Ras modulates Survivin expression independent of hematopoietic growth factors and that a CA-Ras/Survivin axis regulates survival and proliferation of transformed hematopoietic cells.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Cell Cycle / drug effects
  • Cell Cycle / physiology
  • Cell Line
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Enzyme Activation / drug effects
  • Farnesol / analogs & derivatives*
  • Farnesol / pharmacology
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / physiology*
  • Inhibitor of Apoptosis Proteins
  • Interleukin-3 / pharmacology*
  • Mice
  • Microtubule-Associated Proteins / metabolism*
  • Neoplasm Proteins
  • Survivin
  • ras Proteins / antagonists & inhibitors
  • ras Proteins / metabolism*

Substances

  • BIRC5 protein, human
  • Inhibitor of Apoptosis Proteins
  • Interleukin-3
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Survivin
  • farnesylthioacetic acid
  • Farnesol
  • ras Proteins