Division of Biological Science and Technology, Yonsei University, Wonju, Republic of Korea.
Department of Obstetrics and Gynecology, Chung-Ang University School of Medicine, Seoul, Republic of Korea.
PLoS One. 2018 Nov 26;13(11):e0207864. doi: 10.1371/journal.pone.0207864. eCollection 2018.
The expression of hTERT in tumor cells contributes to oncogenic transformation by promoting immortalization. For this reason, hTERT is one of the major targets for cancer therapy, and an efficient method to downregulate hTERT expression is required for treatment of hTERT-positive cancer. In this report, we demonstrated that inhibition of AMP-activated protein kinase (AMPK) downregulates the expression of hTERT. We screened cell signaling pathways in AMPK α1 knockout cells and found that AMPKα1 is required for activity of the hTERT promoter. AMPKα1 knockout cells showed decreased expression of hTERT mRNA and protein. We also demonstrated that compound C, a reversible AMPK inhibitor, suppressed the expression of hTERT. However, AMPK activators, including AICAR and metformin, did not increase the level of hTERT protein. Finally, we showed that tumor cells stably expressing hTERT are resistant to compound C treatment. These results indicate that AMPK activity is required for tumor progression.
端粒酶逆转录酶(hTERT)在肿瘤细胞中的表达通过促进永生化促进致癌转化。出于这个原因,hTERT 是癌症治疗的主要靶点之一,需要一种有效的方法来下调 hTERT 的表达,以治疗 hTERT 阳性癌症。在本报告中,我们证明了抑制 AMP 激活的蛋白激酶(AMPK)可下调 hTERT 的表达。我们筛选了 AMPKα1 敲除细胞中的细胞信号通路,发现 AMPKα1 是 hTERT 启动子活性所必需的。AMPKα1 敲除细胞显示 hTERT mRNA 和蛋白表达减少。我们还证明,可逆 AMPK 抑制剂化合物 C 抑制 hTERT 的表达。然而,AMPK 激活剂,包括 AICAR 和二甲双胍,并没有增加 hTERT 蛋白的水平。最后,我们表明稳定表达 hTERT 的肿瘤细胞对化合物 C 处理具有抗性。这些结果表明 AMPK 活性是肿瘤进展所必需的。