安普克
调节器
蛋白激酶A
AMP活化蛋白激酶
癌细胞
细胞生物学
背景(考古学)
生物
自噬
癌症研究
细胞生长
激酶
癌症
生物化学
遗传学
细胞凋亡
古生物学
基因
作者
Brandon Faubert,Emma E. Vincent,Maya C. Poffenberger,Russell G. Jones
出处
期刊:Cancer Letters
[Elsevier]
日期:2015-01-01
卷期号:356 (2): 165-170
被引量:316
标识
DOI:10.1016/j.canlet.2014.01.018
摘要
The AMP-activated protein kinase (AMPK) is a central regulator of cellular metabolism and energy homeostasis in mammalian tissues. Pertinent to cancer biology is the fact that AMPK is situated in the center of a signaling network involving established tumor suppressors including LKB1, TSC2 and p53. However, recent research suggests that AMPK can exert pro- or anti-tumorigenic roles in cancer depending on context. Loss of AMPK activity has been observed in several tumor types, and can cooperate with oncogenic drivers to reprogram tumor cell metabolism and enhance cell growth and proliferation. However, AMPK activation can also provide a growth advantage to tumor cells by regulating cellular metabolic plasticity, thus providing tumor cells the flexibility to adapt to metabolic stress. Here we discuss the contextual nature of the “two faces” of AMPK in cancer, and discuss the rationale and context for employing AMPK activators versus inhibitors for cancer therapy.
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