Authors: | Zhao, W.; Chang, C.; Cui, Y.; Zhao, X.; Yang, J.; Shen, L.; Zhou, J.; Hou, Z.; Zhang, Z.; Ye, C.; Hasenmayer, D.; Perkins, R.; Huang, X.; Yao, X.; Yu, L.; Huang, R.; Zhang, D.; Guo, H.; Yan, J. |
Article Title: | Steroid receptor coactivator-3 regulates glucose metabolism in bladder cancer cells through coactivation of hypoxia inducible factor 1α |
Abstract: | Background: Steroid receptor coactivator-3 (SRC-3) is frequently overexpressed in human urinary bladder cancer. Results: SRC-3 promotes urinary bladder cancer (UBC) cells proliferation through coactivating HIF1 and up-regulating the expression of genes involved in the glycolytic pathway. Conclusion: SRC-3 plays an important role in UBC development through enhancing glycolysis. Significance: Targeting SRC-3 or enzymes in glycolytic pathway could be an attractive approach in UBC therapy. © 2014 by The American Society for Biochemistry and Molecular Biology, Inc. |
Keywords: | controlled study; human tissue; protein expression; human cell; promoter region; nonhuman; binding affinity; protein function; cell proliferation; mouse; animal tissue; gene; gene expression; protein protein interaction; animal experiment; animal model; bladder cancer; gene expression regulation; cancer cell; lactate dehydrogenase; cycline; steroid receptors; hypoxia inducible factor 1alpha; glycolysis; bladder carcinogenesis; diseases; metabolic regulation; glucose transporter 1; molecular pathology; glucose metabolism; hypoxia-inducible factor 1; steroid receptor coactivator 3; human; priority journal; article; bladder cancer cells; co-activation; glycolytic pathways; urinary bladder cancer; glut1 gene; pgk1 gene |
Journal Title: | Journal of Biological Chemistry |
Volume: | 289 |
Issue: | 16 |
ISSN: | 0021-9258 |
Publisher: | American Society for Biochemistry and Molecular Biology |
Date Published: | 2014-04-18 |
Start Page: | 11219 |
End Page: | 11229 |
Language: | English |
DOI: | 10.1074/jbc.M113.535989 |
PROVIDER: | scopus |
PMCID: | PMC4036260 |
PUBMED: | 24584933 |
DOI/URL: | |
Notes: | J. Biol. Chem. -- Export Date: 2 June 2014 -- CODEN: JBCHA -- Source: Scopus |