ETS Gene Fusions in Prostate Cancer: From Discovery to Daily Clinical Practice

被引:280
作者
Tomlins, Scott A. [1 ]
Bjartell, Anders [2 ]
Chinnaiyan, Arul M. [1 ,3 ]
Jenster, Guido [4 ]
Nam, Robert K. [5 ]
Rubin, Mark A. [6 ]
Schalken, Jack A. [7 ]
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Michigan Ctr Translat Pathol, Ann Arbor, MI 48109 USA
[2] Malmo Univ Hosp, Dept Urol, Malmo, Sweden
[3] Univ Michigan, Sch Med, Dept Urol, Ctr Comprehens Canc,Howard Hughes Med Inst, Ann Arbor, MI USA
[4] Erasmus MC, Dept Urol, Josephine Nefkens Inst, Rotterdam, Netherlands
[5] Sunnybrook Hlth Sci Ctr, Div Urol & Surg Oncol, Toronto, ON M4N 3M5, Canada
[6] Weill Cornell Med Ctr, Dept Pathol & Lab Med, New York, NY USA
[7] Radboud Univ Nijmegen, Med Ctr, Dept Urol, NL-6525 ED Nijmegen, Netherlands
关键词
Prostate cancer; ETS gene fusions; TMPRSS2; Early diagnosis; LEVEL LESS-THAN-OR-EQUAL-TO-4.0 NG; TMPRSS2-ERG FUSION; MYELOID-LEUKEMIA; HGPIN LESIONS; ERG; TRANSCRIPTS; EXPRESSION; REARRANGEMENTS; HETEROGENEITY; PROGRESSION;
D O I
10.1016/j.eururo.2009.04.036
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
Context. In 2005, fusions between the androgen-regulated transmembrane protease serine 2 gene, TMPRSS2, and E twenty-six (ETS) transcription factors were discovered in prostate cancer. Objective: To review advances in our understanding of ETS gene fusions, focusing on challenges affecting translation to clinical application. Evidence acquisition: The PubMed database was searched for reports on ETS fusions in prostate cancer. Evidence synthesis: Since the discovery of ETS fusions, novel 5' and 3' fusion partners and multiple splice isoforms have been reported. The most common fusion, TMPRSS2:ERG, is present in approximately 50% of prostate-specific antigen (PSA)-screened localized prostate cancers and in 15-35% of population-based cohorts. ETS fusions can be detected noninvasively in the urine of men with prostate cancer, with a specificity rate in PSA-screened cohorts of >90%. Reports from untreated population-based cohorts suggest an association between ETS fusions and cancer-specific death and metastatic spread. In retrospective prostatectomy cohorts, conflicting results have been published regarding associations between ETS fusions and cancer aggressiveness. In addition to serving as a potential biomarker, tissue and functional studies suggest a specific role for ETS fusions in the transition to carcinoma. Finally, recent results suggest that the 5' and 3' ends of ETS fusions as well as downstream targets may be targeted therapeutically. Conclusions: Recent studies suggest that the first clinical applications of ETS fusions are likely to be in noninvasive detection of prostate cancer and in aiding with difficult diagnostic cases. Additional studies are needed to clarify the association between gene fusions and cancer aggressiveness, particularly those studies that take into account the multifocal and heterogeneous nature of localized prostate cancer. Multiple promising strategies have been identified to potentially target ETS fusions. Together, these results suggest that ETS fusions will affect multiple aspects of prostate cancer diagnosis and management. (C) 2009 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:275 / 286
页数:12
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