Role of HDAC9-FoxO1 Axis in the Transcriptional Program Associated with Hepatic Gluconeogenesis-Reference-Cited by-同舟云学术

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Role of HDAC9-FoxO1 Axis in the Transcriptional Program Associated with Hepatic Gluconeogenesis

Published:2017-07-21 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Chen Jizheng,Zhang Zhilei,Wang Ning,Guo Min,Chi Xiumei,Pan Yu,Jiang Jing,Niu Junqi,Ksimu Sulaiman,Li John Zhong,Chen Xinwen,Wang Qian

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-06328-3.pdf

Reference37 articles.

1. Magnusson, I., Rothman, D. L., Katz, L. D., Shulman, R. G. & Shulman, G. I. Increased rate of gluconeogenesis in type II diabetes mellitus. A 13C nuclear magnetic resonance study. The Journal of clinical investigation 90, 1323–1327 (1992).

2. Bechmann, L. P. et al. The interaction of hepatic lipid and glucose metabolism in liver diseases. Journal of hepatology 56, 952–964 (2012).

3. Zhang, W. et al. FoxO1 regulates multiple metabolic pathways in the liver: effects on gluconeogenic, glycolytic, and lipogenic gene expression. J Biol Chem 281, 10105–10117 (2006).

4. Yoon, J. C. et al. Control of hepatic gluconeogenesis through the transcriptional coactivator PGC-1. Nature 413, 131–138 (2001).

5. Renga, B. et al. Glucocorticoid receptor mediates the gluconeogenic activity of the farnesoid X receptor in the fasting condition. FASEB journal: official publication of the Federation of American Societies for Experimental Biology 26, 3021–3031 (2012).

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