Exome Sequencing of African-American Prostate Cancer Reveals Loss-of-Function ERF Mutations.
Exome Sequencing of African-American Prostate Cancer Reveals Loss-of-Function ERF Mutations.
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DOI:
10.1158/2159-8290.cd-16-0960
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发表时间:
2017-09
期刊:
影响因子:
28.2
通讯作者:
Garraway LA
中科院分区:
文献类型:
--
作者:
Huang FW;Mosquera JM;Garofalo A;Oh C;Baco M;Amin-Mansour A;Rabasha B;Bahl S;Mullane SA;Robinson BD;Aldubayan S;Khani F;Karir B;Kim E;Chimene-Weiss J;Hofree M;Romanel A;Osborne JR;Kim JW;Azabdaftari G;Woloszynska-Read A;Sfanos K;De Marzo AM;Demichelis F;Gabriel S;Van Allen EM;Mesirov J;Tamayo P;Rubin MA;Powell IJ;Garraway LA
African-American men have the highest incidence and mortality from prostate cancer. Whether a biological basis exists for this disparity remains unclear. Exome sequencing (n=102) and targeted validation (n = 90) of localized primary hormone-naïve prostate cancer in African-American men identified several gene mutations not previously observed in this context, including recurrent loss-of-function mutations in ERF, an ETS transcriptional repressor, in 5% of cases. Analysis of existing prostate cancer cohorts revealed ERF deletions in 3% of primary prostate cancers and mutations or deletions in ERF in 3–5% of lethal castration-resistant prostate cancers. Knockdown of ERF confers increased anchorage-independent growth and generates a gene expression signature associated with oncogenic ETS activation and androgen signaling. Together, these results suggest that ERF is a prostate cancer tumor suppressor gene. More generally, our findings support the application of systematic cancer genomic characterization in settings of broader ancestral diversity to enhance discovery and, eventually, therapeutic applications.