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dc.contributor.authorSethi, G.
dc.contributor.authorShanmugam, M.
dc.contributor.authorKumar, Alan Prem
dc.date.accessioned2018-02-01T05:25:30Z
dc.date.available2018-02-01T05:25:30Z
dc.date.created2018-02-01T04:49:23Z
dc.date.issued2017
dc.identifier.citationSethi, G. and Shanmugam, M. and 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).
dc.identifier.urihttp://hdl.handle.net/20.500.11937/62753
dc.identifier.doi10.1042/BSR20171270
dc.description.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.

dc.titleSREBP-1c as a molecular bridge between lipogenesis and cell cycle progression of clear cell renal carcinoma
dc.typeJournal Article
dcterms.source.volume37
dcterms.source.number6
dcterms.source.issn0144-8463
dcterms.source.titleBioscience Reports
curtin.departmentCurtin Medical School
curtin.accessStatusOpen access via publisher


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