GSK-3β inhibition: At the crossroad between Akt and mTOR constitutive activation to enhance cyclin D1 protein stability in mantle cell lymphoma

Jessica Dal Col, Riccardo Dolcetti

Research output: Contribution to journalArticle

Abstract

Strategies able to downregulate the aberrant expression of cyclin D1 may prove of therapeutic relevance in cancer patients. This is particularly true for mantle cell lymphoma (MCL) in which cyclin D1 is overexpressed as a consequence of the t(11;14)(q13;q32) translocation. We have recently demonstrated that an increased cyclin D1 stability also contributes to the high levels of this protein observed in MCL cells. This effect is mediated by a constitutive activation of PI3-K/Akt, which keeps GSK-3β inhibited. Here we show that inhibition of PI3-K/Akt induces a 40% decrease of cyclin D1 half-life as a result of accumulation of the dephosphorylated/active form of GSK-3β within the nucleus, where this kinase can phosphorylate cyclin D1 on Thr286 thereby promoting its nuclear export. Translocation of cyclin D1 into the cytoplasm is mediated by the nuclear exportin CRM1, whose association with cyclin D1 increases following PI3-K/Akt inhibition. Notably, rapamycin downregulated GSK-3β Ser9 phosphorylation with concurrent nuclear export of cyclin D1 only in MCL cells in which GSK-3β is under the control of mTOR. These findings suggest that the ability to downregulate cyclin D1 through GSK-3β may identify subsets of MCL patients who may benefit from the treatment with mTOR inhibitors and stimulate further studies to assess whether the inability to affect GSK-3β activity may constitute a clinically relevant resistance factor to mTOR inhibitors.

Original languageEnglish
Pages (from-to)2813-2816
Number of pages4
JournalCell Cycle
Volume7
Issue number18
Publication statusPublished - Sep 15 2008

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Keywords

  • Akt
  • CRM1
  • Cyclin D1
  • Glycogen synthase kinase 3β
  • Mantle cell lymphoma
  • mTOR
  • Nuclear export
  • Phosphatidyl-inositol-3 kinase
  • PTEN

ASJC Scopus subject areas

  • Cell Biology
  • Biochemistry
  • Molecular Biology
  • Medicine(all)

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