Hussain A R, Al-Rasheed M, Manogaran P S, Al-Hussein K A, Platanias L C, Al Kuraya K, Uddin S
King Fahad National Center for Children's Cancer and Research, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Apoptosis. 2006 Feb;11(2):245-54. doi: 10.1007/s10495-006-3392-3.
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.
姜黄素已被证明具有多种生物学功能,包括抗肿瘤活性。姜黄素抑制细胞增殖的机制仍知之甚少。在本报告中,我们研究了姜黄素对T细胞急性淋巴细胞白血病(T-ALL)恶性细胞凋亡途径激活的影响。我们的数据表明,姜黄素在几种T细胞系中引起剂量依赖性的增殖抑制。姜黄素处理导致组成型活性AKT、FOXO转录因子和GSK3的去磷酸化/失活。姜黄素还诱导细胞色素c的释放,同时激活caspase-3并切割PARP。此外,caspase的通用抑制剂zVAD-fmk可防止caspase-3激活,并消除姜黄素处理诱导的细胞死亡。最后,用姜黄素处理T-ALL细胞可下调凋亡抑制蛋白(IAPs)的表达。综上所述,我们的研究结果表明,姜黄素抑制T细胞中PI3'-激酶的组成型激活靶点(AKT、FOXO和GSK3),导致增殖抑制和caspase依赖性凋亡的诱导。