You Mengli, Jin Jianhua, Liu Qian, Xu QingGang, Shi Juanjuan, Hou Yongzhong
Department of Oncology, The Affiliated Wujin People's Hospital, Jiangsu University, Changzhou 213162, Jiangsu Province, People's Republic of China.
Institute of Life Science, Jiangsu University, Zhenjiang 212000, Jiangsu Province, People's Republic of China.
J Cell Biochem. 2017 Jun;118(6):1556-1562. doi: 10.1002/jcb.25817. Epub 2017 Jan 5.
Abundant nutrient availability including glucose and amino acids plays an important role in maintaining cancer cell energetic and biosynthetic pathways. As a nuclear receptor, peroxisome-proliferator-activated receptor α (PPARα) regulates inflammation and cancer progression, however, it is still unclear the interaction of PPARα with the cancer cell glucose metabolism. Here we found that PPARα reduced Glut1 (Glucose transporter 1) protein and gene levels in HCT-116, SW480, HeLa, and MCF-7 cancer cell lines. In contrast, silenced PPARα reversed this event. Further analysis shows that PPARα directly targeted the consensus PPRE motif of Glut1 promoter region resulting in Glut1 transcription repression. PPARα-mediated Glut1 transcription repression led to decreased influx of glucose in cancer cells. These findings revealed a novel mechanism of PPARα-mediated cancer cell Glut1 transcription repression. J. Cell. Biochem. 118: 1556-1562, 2017. © 2016 Wiley Periodicals, Inc.
包括葡萄糖和氨基酸在内的丰富营养物质供应在维持癌细胞的能量代谢和生物合成途径中起着重要作用。作为一种核受体,过氧化物酶体增殖物激活受体α(PPARα)调节炎症和癌症进展,然而,PPARα与癌细胞葡萄糖代谢之间的相互作用仍不清楚。在这里,我们发现PPARα降低了HCT-116、SW480、HeLa和MCF-7癌细胞系中Glut1(葡萄糖转运蛋白1)的蛋白质和基因水平。相反,沉默PPARα可逆转这一现象。进一步分析表明,PPARα直接靶向Glut1启动子区域的共有PPRE基序,导致Glut1转录受到抑制。PPARα介导的Glut1转录抑制导致癌细胞中葡萄糖内流减少。这些发现揭示了PPARα介导的癌细胞Glut1转录抑制的新机制。《细胞生物化学杂志》118: 1556 - 1562, 2017。© 2016威利期刊公司