Calcium Channel Blocker Use and Risk Prostate Cancer by TMPRSS2: ERG Gene Fusion Status

被引:17
作者
Geybels, Milan S. [1 ,2 ]
McCloskey, Karen D. [3 ]
Mills, Ian G. [3 ]
Stanford, Janet L. [1 ,4 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, 1100 Fairview Ave N, Seattle, WA 98109 USA
[2] Maastricht Univ, GROW Sch Oncol & Dev Biol, Dept Epidemiol, Maastricht, Netherlands
[3] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Belfast, Antrim, North Ireland
[4] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98195 USA
关键词
prostate cancer; calcium channel blockers; TMPRSS2: ERG gene fusion; risk; Gleason score; ANTIHYPERTENSIVE DRUG-USE; CELL-PROLIFERATION; ASSOCIATION; PROTEIN; HYPERTENSION; EXPRESSION; RECEPTOR; CA(V)1.3;
D O I
10.1002/pros.23267
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Calcium channel blockers (CCBs) may affect prostate cancer (PCa) growth by various mechanisms including those related to androgens. The fusion of the androgen-regulated gene TMPRSS2 and the oncogene ERG (TMPRSS2: ERG or T2E) is common in PCa, and prostate tumors that harbor the gene fusion are believed to represent a distinct disease subtype. We studied the association of CCB use with the risk of PCa, and molecular subtypes of PCa defined by T2E status. METHODS. Participants were residents of King County, Washington, recruited for population-based case-control studies (1993-1996 or 2002-2005). Tumor T2E status was determined by fluorescence in situ hybridization using tumor tissue specimens from radical prostatectomy. Detailed information on use of CCBs and other variables was obtained through inperson interviews. Binomial and polytomous logistic regression were used to generate odds ratios (ORs) and 95% confidence intervals (CIs). RESULTS. The study included 1,747 PCa patients and 1,635 age-matched controls. A subset of 563 patients treated with radical prostatectomy had T2E status determined, of which 295 were T2E positive (52%). Use of CCBs (ever vs. never) was not associated with overall PCa risk. However, among European-American men, users had a reduced risk of higher-grade PCa (Gleason scores >= 7: adjusted OR = 0.64; 95% CI: 0.44-0.95). Further, use of CCBs was associated with a reduced risk of T2E positive PCa (adjusted OR = 0.38; 95% CI: 0.19-0.78), but was not associated with T2E negative PCa. CONCLUSIONS. This study found suggestive evidence that use of CCBs is associated with reduced relative risks for higher Gleason score and T2E positive PCa. Future studies of PCa etiology should consider etiologic heterogeneity as PCa subtypes may develop through different causal pathways. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:282 / 290
页数:9
相关论文
共 49 条
[1]   The Molecular Taxonomy of Primary Prostate Cancer [J].
Abeshouse, Adam ;
Ahn, Jaeil ;
Akbani, Rehan ;
Ally, Adrian ;
Amin, Samirkumar ;
Andry, Christopher D. ;
Annala, Matti ;
Aprikian, Armen ;
Armenia, Joshua ;
Arora, Arshi ;
Auman, J. Todd ;
Balasundaram, Miruna ;
Balu, Saianand ;
Barbieri, Christopher E. ;
Bauer, Thomas ;
Benz, Christopher C. ;
Bergeron, Alain ;
Beroukhim, Rameen ;
Berrios, Mario ;
Bivol, Adrian ;
Bodenheimer, Tom ;
Boice, Lori ;
Bootwalla, Moiz S. ;
dos Reis, Rodolfo Borges ;
Boutros, Paul C. ;
Bowen, Jay ;
Bowlby, Reanne ;
Boyd, Jeffrey ;
Bradley, Robert K. ;
Breggia, Anne ;
Brimo, Fadi ;
Bristow, Christopher A. ;
Brooks, Denise ;
Broom, Bradley M. ;
Bryce, Alan H. ;
Bubley, Glenn ;
Burks, Eric ;
Butterfield, Yaron S. N. ;
Button, Michael ;
Canes, David ;
Carlotti, Carlos G. ;
Carlsen, Rebecca ;
Carmel, Michel ;
Carroll, Peter R. ;
Carter, Scott L. ;
Cartun, Richard ;
Carver, Brett S. ;
Chan, June M. ;
Chang, Matthew T. ;
Chen, Yu .
CELL, 2015, 163 (04) :1011-1025
[2]   Statin use and risk of prostate cancer: Results from a population-based epidemiologic study [J].
Agalliu, Ilir ;
Salinas, Claudia A. ;
Hansten, Philip D. ;
Ostrander, Elaine A. ;
Stanford, Janet L. .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2008, 168 (03) :250-260
[3]   Prostate cancer [J].
Attard, Gerhardt ;
Parker, Chris ;
Eeles, Ros A. ;
Schroder, Fritz ;
Tomlins, Scott A. ;
Tannock, Ian ;
Drake, Charles G. ;
de Bono, Johann S. .
LANCET, 2016, 387 (10013) :70-82
[4]   The role of L-type voltage-gated calcium channels Cav1.2 and Cav1.3 in normal and pathological brain function [J].
Berger, Stefan M. ;
Bartsch, Dusan .
CELL AND TISSUE RESEARCH, 2014, 357 (02) :463-476
[5]   Expression of the Androgen-Regulated Fusion Gene TMPRSS2-ERG Does Not Predict Response to Endocrine Treatment in Hormone-Naive, Node-Positive Prostate Cancer [J].
Boormans, Joost L. ;
Hermans, Karin G. ;
Ziel-van der Made, Angelique C. J. ;
van Leenders, Geert J. H. L. ;
Wildhagen, Mark F. ;
Collette, Laurence ;
Schroeder, Fritz H. ;
Trapman, Jan ;
Verhagen, Paul C. M. S. .
EUROPEAN UROLOGY, 2010, 57 (05) :830-835
[6]   CaV channels and cancer: canonical functions indicate benefits of repurposed drugs as cancer therapeutics [J].
Buchanan, Paul J. ;
McCloskey, Karen D. .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2016, 45 (07) :621-633
[7]   Cav1.3 channel α1D protein is overexpressed and modulates androgen receptor transactivation in prostate cancers [J].
Chen, Ruibao ;
Zeng, Xing ;
Zhang, Ruitao ;
Huang, Jiaoti ;
Kuang, Xiangxing ;
Yang, Jun ;
Liu, Jihong ;
Tawfik, Ossama ;
Thrasher, James Brantley ;
Li, Benyi .
UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2014, 32 (05) :524-536
[8]   Role of the TMPRSS2-ERG gene fusion in prostate cancer [J].
Chinnaiyan, Arul M. .
NEOPLASIA, 2008, 10 (02) :177-U23
[9]   Calcium signaling [J].
Clapham, David E. .
CELL, 2007, 131 (06) :1047-1058
[10]   ETS gene fusions in prostate cancer [J].
Clark, Jeremy P. ;
Cooper, Colin S. .
NATURE REVIEWS UROLOGY, 2009, 6 (08) :429-439