Activation of the p70 S6 kinase by all-trans-retinoic acid in acute promyelocytic leukemia cells

Blood. 2005 Feb 15;105(4):1669-77. doi: 10.1182/blood-2004-06-2078. Epub 2004 Oct 7.

Abstract

Although the mechanisms by which all-trans-retinoic acid (RA) regulates gene transcription are well understood, very little is known on the signaling events regulating RA-dependent initiation of mRNA translation. We examined whether the mammalian target of rapamycin (mTOR)/p70 S6 kinase pathway is activated by RA. RA treatment of sensitive cell lines resulted in phosphorylation/activation of mTOR and downstream induction of p70 S6 kinase activity. Such phosphorylation/activation of p70 S6 kinase was inducible in primary acute promyelocytic leukemia (APL) blasts and RA-sensitive NB-4 cells, but was defective in an NB-4 variant cell line (NB-4.007/6) that is resistant to the biologic effects of RA. The RA-dependent activation of p70 S6 kinase was also phosphatidylinositol 3' kinase (PI3'K)-dependent, and resulted in downstream phosphorylation of the S6 ribosomal protein on Ser235/236 and Ser240/244, events important for initiation of translation for mRNAs with oligopyrimidine tracts in their 5' untranslated region. RA treatment of leukemia cells also resulted in an mTOR-mediated phosphorylation of the 4E-BP1 repressor of mRNA translation, to induce its deactivation and dissociation from the eukaryotic initiation factor-4E (eIF-4E) complex. Altogether, these findings provide evidence for the existence of a novel RA-activated cellular pathway that regulates cap-dependent translation, and strongly suggest that this cascade plays a role in the induction of retinoid responses in APL cells.

Publication types

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

MeSH terms

  • Cell Differentiation / physiology
  • Cell Line, Tumor
  • Enzyme Activation
  • Eukaryotic Initiation Factor-4E / metabolism
  • Growth Inhibitors / pharmacology
  • Humans
  • Leukemia, Promyelocytic, Acute / enzymology*
  • Leukemia, Promyelocytic, Acute / metabolism
  • Leukemia, Promyelocytic, Acute / pathology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation
  • Protein Kinases / metabolism
  • Protein Kinases / physiology
  • RNA Caps / metabolism
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism*
  • Ribosomal Protein S6 Kinases, 70-kDa / physiology
  • Serine / metabolism
  • Signal Transduction / physiology
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases
  • Tretinoin / pharmacology*

Substances

  • Eukaryotic Initiation Factor-4E
  • Growth Inhibitors
  • RNA Caps
  • Serine
  • Tretinoin
  • Protein Kinases
  • MTOR protein, human
  • Ribosomal Protein S6 Kinases, 70-kDa
  • TOR Serine-Threonine Kinases
  • Sirolimus