Glycolysis maintains AMPK activation in sorafenib-induced Warburg effect

被引:13
作者
Guo, Sijia [1 ]
Zhang, Chenhao [1 ]
Zeng, Haiou [2 ]
Xia, Yantao [3 ]
Weng, Chenghao [1 ]
Deng, Yichen [1 ]
Wang, Luda [2 ]
Wang, Huan [1 ,4 ]
机构
[1] Peking Univ, Beijing Key Lab Tumor Syst Biol, Sch Basic Med Sci, Inst Syst Biomed,Hlth Sci Ctr, Beijing 100191, Peoples R China
[2] Peking Univ, Sch Integrated Circuit, Natl Key Lab Sci & Technol Micro Nano Fabricat, Beijing 100871, Peoples R China
[3] Univ Calif Los Angeles, Dept Chem & Biomol Engn, Los Angeles, CA 90095 USA
[4] Peking Univ, Hlth Sci Ctr, 38 Xueyuan Rd, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
AMPK; Hepatocellular carcinoma; Glycolysis; Drug sensitivity; Sorafenib; PROTEIN-KINASE; HCC CELLS; RESISTANCE; GLUCOSE; PHOSPHORYLATION; INHIBITION; MECHANISMS; UPSTREAM; ACTS; BETA;
D O I
10.1016/j.molmet.2023.101796
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hepatocellular carcinoma (HCC) is the second deadly cancer in the world and still lacks curative treatment. Aerobic glycolysis, or Warburg effect, is a major resistance mechanism induced by first-line treatment of HCC, sorafenib, and is regulated by the master regulator of metabolism, AMPK. Activation of AMPK is required for resistance; however, activation dynamics of AMPK and its regulation is rarely studied. Engineering cells to express an AMPK activity biosensor, we monitor AMPK activation in single HCC cells in a high throughput manner during sorafenib-induced drug resistance. Sorafenib induces transient activation of AMPK, duration of which is dependent on glucose. Inhibiting glycolysis shortens AMPK activation; whereas increasing glycolysis increases its activation duration. Our data highlight that activation duration of AMPK is important for cancer evasion of therapeutic treatment and glycolysis is a key regulator of activation duration of AMPK. (c) 2023 Published by Elsevier GmbH. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
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页数:10
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