Please use this identifier to cite or link to this item: https://doi.org/10.1042/BSR20171270
Title: SREBP-1c as a molecular bridge between lipogenesis and cell cycle progression of clear cell renal carcinoma
Authors: Sethi, G 
Shanmugam, M.K 
Kumar, A.P 
Keywords: protein RNF20
RING finger protein
securin
sterol regulatory element binding protein 1c
unclassified drug
sterol regulatory element binding protein 1
carcinogenesis
cell cycle progression
cell cycle regulation
down regulation
human
lipid metabolism
lipid storage
lipogenesis
nonhuman
renal cell carcinoma
Review
upregulation
cell cycle
genetics
lipogenesis
liver
metabolism
pathology
renal cell carcinoma
Carcinogenesis
Carcinoma, Renal Cell
Cell Cycle
Humans
Lipid Metabolism
Lipogenesis
Liver
Sterol Regulatory Element Binding Protein 1
Issue Date: 2017
Publisher: Portland Press Ltd
Citation: Sethi, G, Shanmugam, M.K, Kumar, A.P (2017). SREBP-1c as a molecular bridge between lipogenesis and cell cycle progression of clear cell renal carcinoma. Bioscience Reports 37 (6) : BSR20171270. ScholarBank@NUS Repository. https://doi.org/10.1042/BSR20171270
Rights: Attribution 4.0 International
Abstract: Sterol regulatory element binding protein 1c (SREBP-1c) promotes lipogenesis and tumor growth in various cancers. It is well known that clear cell renal cell carcinoma (ccRCC), a major subtype of the kidney cancers, exhibits elevated lipid accumulation. However, it has not been fully understood how lipid metabolism might be associated with cell cycle regulation in ccRCC. In a recent issue, Lee et al. (Molecular and Cellular Biology (2017) pii: MCB.00265-17) demonstrate that SREBP-1c is up-regulated in ccRCC by ring finger protein 20 (RNF20) down-regulation, leading to aberrant lipid storage and pituitary tumor transforming gene 1 (PTTG1)-dependent cell cycle progression. These findings suggest that SREBP-1c serves as a molecular bridge between lipid metabolism and cell cycle control in ccRCC tumorigenesis.
Source Title: Bioscience Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/179069
ISSN: 01448463
DOI: 10.1042/BSR20171270
Rights: Attribution 4.0 International
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