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Curcumin induces apoptosis via inhibition of PI3′-kinase/AKT pathway in acute T cell leukemias

  • Azhar Hussain
  • , M. Al-Rasheed
  • , P. S. Manogaran
  • , K. A. Al-Hussein
  • , L.C. Platanias
  • , K. Al Kuraya
  • , S. Uddin

Research output: Contribution to journalArticle

Abstract

Curcumin has been shown to possess variety of biological functions including anti-tumor activity. The mechanism by which curcumin inhibit cell proliferation remains poorly understood. In the present report, we investigated the effect of curcumin on the activation of apoptotic pathway in T-cell acute lymphoblastic leukemia (T-ALL) malignant cells. Our data demonstrate that curcumin causes dose dependent suppression of proliferation in several T cell lines. Curcumin treatment causes the de-phosphorylation/inactivation of constitutively active AKT, FOXO transcription factor and GSK3. Curcumin also induces release of cytochrome c accompanied by activation of caspase-3 and PARP cleavage. In addition, zVAD-fmk, a universal inhibitor of caspases, prevents caspase-3 activation and abrogates cell death induced by curcumin treatment. Finally, treatment of T-ALL cells with curcumin down-regulated the expression of inhibitor of apoptosis protein (IAPs). Taken together, our finding suggest that curcumin suppresses constitutively activated targets of PI3′-kinase (AKT, FOXO and GSK3) in T cells leading to the inhibition of proliferation and induction of caspase-dependent apoptosis.

Original languageUndefined/Unknown
JournalApoptosis
Publication statusPublished - 1 Jan 2006

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