Recurrent fusion of TMPRSS2 and ETS transcription factor genes in prostate cancer

被引:2985
作者
Tomlins, SA
Rhodes, DR
Perner, S
Dhanasekaran, SM
Mehra, R
Sun, XW
Varambally, S
Cao, XH
Tchinda, J
Kuefer, R
Lee, C
Montie, JE
Shah, RB
Pienta, KJ
Rubin, MA
Chinnaiyan, AM
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Bioinformat Program, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Sch Med, Michigan Urol Ctr, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Sch Med, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[7] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[8] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[9] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[10] Univ Ulm, Fac Med, Dept Urol, D-89075 Ulm, Germany
关键词
D O I
10.1126/science.1117679
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recurrent chromosomal rearrangements have not been well characterized in common carcinomas. We used a bioinformatics approach to discover candidate oncogenic chromosomal aberrations on the basis of outlier gene expression. Two ETS transcription factors, ERG and ETV1, were identified as outliers in prostate cancer. We identified recurrent gene fusions of the 5' untranslated region of TMPRSS2 to ERG or ETV1 in prostate cancer tissues with outlier expression. By using fluorescence in situ hybridization, we demonstrated that 23 of 29 prostate cancer samples harbor rearrangements in ERG or ETV1. Cell line experiments suggest that the androgen-responsive promoter elements of TMPRSS2 mediate the overexpression of ETS family members in prostate cancer. These results have implications in the development of carcinomas and the molecular diagnosis and treatment of prostate cancer.
引用
收藏
页码:644 / 648
页数:5
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