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The double-edged sword of AMPK signaling in cancer and its therapeutic implications

期刊

ARCHIVES OF PHARMACAL RESEARCH
卷 38, 期 3, 页码 346-357

出版社

PHARMACEUTICAL SOC KOREA
DOI: 10.1007/s12272-015-0549-z

关键词

AMPK; LKB1; CAMKK2; mTORC1; ACC; NADPH; ROS; Fatty acids; Metabolic stress; Mitochondria; Biguanides; Cancer

资金

  1. National R&D Program for Cancer Control, Ministry of Health & Welfare, Republic of Korea [S2014-A0251-00001]
  2. National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [S2014-A0403-00067]
  3. Korea Health Promotion Institute [1420320] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

5'-AMP-activated protein kinase (AMPK) plays a pivotal role in maintaining energy and redox homeostasis under various metabolic stress conditions. Metabolic adaptation, which can be triggered by the activation of AMPK during metabolic stress, is the critical process for cell survival through the maintenance of ATP and NADPH levels. The importance of such regulation of fundamental process poses the AMPK signaling pathway in one of the most attractive therapeutic targets in many pathologies such as diabetes and cancer. In cancer, however, accumulating data suggest that the role of AMPK would not be simply defined as anti-or pro-tumorigenic, but it seems to have two faces like a double-edged sword. Importantly, recent studies showed that the anti-tumorigenic effects of many 'indirect' AMPK activators such as anti-diabetic biguanides are not dependent on AMPK; rather the activation of AMPK induces the resistance to their cytotoxic effects, emphasizing the pro-tumorigenic effect of AMPK. In this review, we summarize and discuss recent findings suggesting the two faces of AMPK in cancer, and discuss how we can exploit this unique feature of AMPK for novel therapeutic intervention.

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