Casimiro Mathew C, Di Sante Gabriele, Di Rocco Agnese, Loro Emanuele, Pupo Claudia, Pestell Timothy G, Bisetto Sara, Velasco-Velázquez Marco A, Jiao Xuanmao, Li Zhiping, Kusminski Christine M, Seifert Erin L, Wang Chenguang, Ly Daniel, Zheng Bin, Shen Che-Hung, Scherer Philipp E, Pestell Richard G
Pennsylvania Cancer and Regenerative Medicine Research Center (PCARM), Doylestown, Pennsylvania.
Pennsylvania Biotechnology Center of Bucks County at Baruch S. Blumberg Institute, Doylestown, Pennsylvania.
Cancer Res. 2017 Jul 1;77(13):3391-3405. doi: 10.1158/0008-5472.CAN-16-0425. Epub 2017 May 18.
Autophagy activated after DNA damage or other stresses mitigates cellular damage by removing damaged proteins, lipids, and organelles. Activation of the master metabolic kinase AMPK enhances autophagy. Here we report that cyclin D1 restrains autophagy by modulating the activation of AMPK. In cell models of human breast cancer or in a cyclin D1-deficient model, we observed a cyclin D1-mediated reduction in AMPK activation. Mechanistic investigations showed that cyclin D1 inhibited mitochondrial function, promoted glycolysis, and reduced activation of AMPK (pT172), possibly through a mechanism that involves cyclin D1-Cdk4/Cdk6 phosphorylation of LKB1. Our findings suggest how AMPK activation by cyclin D1 may couple cell proliferation to energy homeostasis. .
DNA损伤或其他应激后激活的自噬通过清除受损蛋白质、脂质和细胞器来减轻细胞损伤。主要代谢激酶AMPK的激活可增强自噬。在此,我们报告细胞周期蛋白D1通过调节AMPK的激活来抑制自噬。在人乳腺癌细胞模型或细胞周期蛋白D1缺陷模型中,我们观察到细胞周期蛋白D1介导的AMPK激活减少。机制研究表明,细胞周期蛋白D1抑制线粒体功能,促进糖酵解,并降低AMPK(pT172)的激活,这可能是通过一种涉及细胞周期蛋白D1-Cdk4/Cdk6对LKB1磷酸化的机制实现的。我们的研究结果表明细胞周期蛋白D1激活AMPK可能如何将细胞增殖与能量稳态联系起来。