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공공누리This item is licensed Korea Open Government License

dc.contributor.author
CalebF.Davis
dc.contributor.author
강효진
dc.contributor.author
이준학
dc.date.accessioned
2019-08-28T07:41:38Z
dc.date.available
2019-08-28T07:41:38Z
dc.date.issued
2014-09-08
dc.identifier.issn
1535-6108
dc.identifier.uri
https://repository.kisti.re.kr/handle/10580/14357
dc.identifier.uri
http://www.ndsl.kr/ndsl/search/detail/article/articleSearchResultDetail.do?cn=NART70271342
dc.description.abstract
We describe the landscape of somatic genomic alterations of 66 chromophobe renal cell carcinomas (ChRCCs) on the basis of multidimensional and comprehensive characterization, including mtDNA and whole-genome sequencing. The result is consistent that ChRCC originates from the distal nephron compared with other kidney cancers with more proximal origins. Combined mtDNA and gene expression analysis implicates changes in mitochondrial function as a component of the disease biology, while suggesting alternative roles for mtDNA mutations in cancers relying on oxidative phosphorylation. Genomic rearrangements lead to recurrent structural breakpoints within TERT promoter region, which correlates with highly elevated TERT expression and manifestation of kataegis, representing a mechanism of TERT upregulation in cancer distinct from previously observed amplifications and point mutations.
dc.language
eng
dc.relation.ispartofseries
Cancer cell
dc.title
The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma
dc.subject.keyword
kidney cancer
dc.subject.keyword
mutation
dc.subject.keyword
chromophobe renal cell carcinoma
dc.subject.keyword
whole genome sequence
dc.subject.keyword
TERT
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7. KISTI 연구성과 > 학술지 발표논문
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