TMPRSS2-ERG fusion heterogeneity in Multifocal prostate cancer: Clinical and biologic implications

被引:129
作者
Barry, Marc
Perner, Sven
Demichelis, Francesca
Rubin, Mark A.
机构
[1] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Cambridge, MA 02138 USA
[3] Univ Ulm, Dept Pathol, Ulm, Germany
[4] ITC irst, SRA Div, Bioinformat Grp, Povo, Trento, Italy
[5] MIT, Broad Inst, Cambridge, MA 02139 USA
[6] Dana Farber Harvard Comprehens Canc Ctr, Boston, MA USA
关键词
D O I
10.1016/j.urology.2007.08.032
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES To characterize the clonality of TMPRSS2-ERG fusion in multifocal prostate cancer. METHODS From 80 consecutive radical prostatectomy specimens, we identified 32 cases with multiple spatially separate tumors. In each case, we assessed two to three tumor foci for TMPRSS2-ERG fusion using an ERG break-apart interphase fluorescence in situ hybridization assay. RESULTS Individual tumor foci showed homogenity for fusion status (intrafocal clonal homogenity). In 19 (59%) of the 32 cases, all foci within a case had the same fusion status (interfocal homogeneity). In 15 (80%) of the 19 cases, no foci had fusion, and in 4 (20%), all foci had fusion. Of the 32 cased, 13 (41%) demonstrated heterogeneity for fusion status within a case (interfocal clonal heterogeneity). CONCLUSIONS In this study, we have demonstrated interfocal heterogeneity and intrafocal homogeneity for TMPRSS2-ERG fusion in prostate cancer with multiple tumors. These findings support the multiclonal nature of prostate cancer with clinical implications for needle biopsy strategies and the development of urine-based screening tests.
引用
收藏
页码:630 / 633
页数:4
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