Hardie D G
Division of Cell Signalling and Immunology, College of Life Sciences, University of Dundee, Dundee DD1 5EH, United Kingdom.
Cold Spring Harb Symp Quant Biol. 2011;76:155-64. doi: 10.1101/sqb.2011.76.010819. Epub 2011 Nov 9.
Adenosine monophosphate-activated protein kinase (AMPK) is a cellular energy sensor activated by metabolic stresses that inhibit catabolic ATP production or accelerate ATP consumption. Once activated, AMPK switches on catabolic pathways, generating ATP, while inhibiting cell growth and proliferation, thus promoting energy homeostasis. AMPK is activated by the antidiabetic drug metformin, and by many natural products including "nutraceuticals" and compounds used in traditional medicines. Most of these xenobiotics activate AMPK by inhibiting mitochondrial ATP production. AMPK activation by metabolic stress requires the upstream kinase, LKB1, whose tumor suppressor effects may be largely mediated by AMPK. However, many tumor cells appear to have developed mechanisms to reduce AMPK activation and thus escape its growth-restraining effects. A similar phenomenon occurs during viral infection. If we can establish how down-regulation occurs in tumors and virus-infected cells, there may be therapeutic avenues to reverse these effects.
腺苷单磷酸激活的蛋白激酶(AMPK)是一种细胞能量传感器,可被抑制分解代谢性ATP产生或加速ATP消耗的代谢应激所激活。一旦被激活,AMPK就会开启分解代谢途径,生成ATP,同时抑制细胞生长和增殖,从而促进能量稳态。抗糖尿病药物二甲双胍以及许多天然产物(包括“营养保健品”和传统药物中使用的化合物)均可激活AMPK。这些外源性物质大多通过抑制线粒体ATP产生来激活AMPK。代谢应激激活AMPK需要上游激酶LKB1,其肿瘤抑制作用可能很大程度上是由AMPK介导的。然而,许多肿瘤细胞似乎已经形成了降低AMPK激活的机制,从而逃避其生长抑制作用。病毒感染期间也会出现类似现象。如果我们能够确定肿瘤细胞和病毒感染细胞中AMPK下调是如何发生的,那么可能会有逆转这些效应的治疗途径。