| Literature DB >> 27918085 |
Mengli You1,2, Jianhua Jin1, Qian Liu1, QingGang Xu2, Juanjuan Shi2, Yongzhong Hou1,2.
Abstract
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.Entities:
Keywords: CELL SIGNALING; GLUT1; PPARα; TRANSCRIPTION REPRESSION
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Year: 2017 PMID: 27918085 DOI: 10.1002/jcb.25817
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429