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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 |
Appears in Collections: | Staff Publications Elements |
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