INSERM, U1065, Centre Méditerranéen de Médecine Moléculaire (C3M), Equipe 4: Inflammation, Cancer, Cellules Souches Cancéreuses, Nice F-06204, France.
Cancer Lett. 2013 Aug 9;336(1):114-26. doi: 10.1016/j.canlet.2013.04.015. Epub 2013 Apr 21.
We show here that the antidiabetic agents metformin and phenformin and the AMPK activator AICAR exert strong anti-tumoural effects on tPTEN-/- lymphoma cells and on human T-ALL cell lines and primary samples. The compounds act by inhibiting tumour metabolism and proliferation and by inducing apoptosis in parallel with an activation of AMPK and an inhibition of constitutive mTOR. In tPTEN-/- cells, the drugs potentiated the anti-leukaemic effects of dexamethasone, and metformin and phenformin synergised with 2-deoxyglucose (2DG) to impair tumour cell survival. In vivo, metformin and AICAR strongly decreased the growth of luciferase-expressing tPTEN-/- cells xenografted in Nude mice, demonstrating that metabolism targeting could be a potent adjuvant strategy for lymphoma/leukaemia treatment.
我们在这里表明,抗糖尿病药物二甲双胍和苯乙双胍以及 AMPK 激活剂 AICAR 对 tPTEN-/-淋巴瘤细胞和人 T-ALL 细胞系和原代样本具有强烈的抗肿瘤作用。这些化合物通过抑制肿瘤代谢和增殖,并通过平行激活 AMPK 和抑制组成型 mTOR 来诱导细胞凋亡。在 tPTEN-/-细胞中,这些药物增强了地塞米松的抗白血病作用,二甲双胍和苯乙双胍与 2-脱氧葡萄糖(2DG)协同作用,损害肿瘤细胞的存活。在体内,二甲双胍和 AICAR 强烈抑制了在 Nude 小鼠中异种移植的表达荧光素酶的 tPTEN-/-细胞的生长,证明代谢靶向可能是淋巴瘤/白血病治疗的一种有效辅助策略。
Am J Physiol Endocrinol Metab. 2004-8
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