Prospective Study of Seroreactivity to JC Virus T-Antigen and Risk of Colorectal Cancers and Adenomas

被引:9
|
作者
Hampras, Shalaka S. [1 ]
Viscidi, Raphael P. [2 ]
Helzlsouer, Kathy J. [3 ]
Lee, Ji-Hyun [4 ]
Fulp, William J. [5 ]
Giuliano, Anna R. [1 ]
Platz, Elizabeth A. [6 ]
Rollison, Dana E. [1 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Canc Epidemiol, Tampa, FL 33612 USA
[2] Johns Hopkins Sch Med, Dept Pediat, Baltimore, MD USA
[3] Mercy Med Ctr, Ctr Prevent & Res, Baltimore, MD USA
[4] Univ New Mexico, Ctr Canc, Albuquerque, NM 87131 USA
[5] H Lee Moffitt Canc Ctr & Res Inst, Dept Biostat, Tampa, FL 33612 USA
[6] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
关键词
METHYLATOR PHENOTYPE; DNA-SEQUENCES; POLYOMAVIRUS; EXPRESSION; CARCINOMA; BK; ASSOCIATION; AGNOPROTEIN; INFECTION; COLON;
D O I
10.1158/1055-9965.EPI-14-0370
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
John Cunningham virus (JCV) is a common polyomavirus classified as a possible carcinogen by the International Agency for Research on Cancer. JCV may play a role in colorectal carcinogenesis, although we previously reported no association between JCV capsid antibodies and colorectal cancer. No studies have examined the role of seroreactivity to JCV T-antigen (T-Ag) oncoprotein in colorectal cancer. A case-control study nested within a community-based prospective cohort (CLUE II) was conducted. In 1989, 25,080 residents of Washington County, Maryland, were enrolled in CLUE II, completing baseline questionnaires and providing blood samples. At follow-up, 257 incident colorectal cancer cases were identified by linkage to population-based cancer registries through 2006 and matched to controls on age, sex, race, and date of blood draw. One hundred and twenty-three colorectal adenoma cases were identified through self-report during follow-up and matched to controls on age, sex, race, date of blood draw, and colorectal cancer screening. Baseline serum samples were tested for seroreactivity to JCV T-Ag. Associations between JCV T-Ag seroreactivity and colorectal cancer/adenomas were evaluated using conditional logistic regression models. Overall, seroreactivity to JCV T-Ag was not statistically significantly associated with the risk of either colorectal cancer [OR, 1.34; 95% confidence interval (CI), 0.89-2.01] or adenoma (OR, 1.30; 95% CI, 0.70-2.42), while a borderline association with colorectal cancer was observed among women (OR, 1.82; 95% CI, 1.00-3.31). Our past evaluation of JCV capsid seropositivity, combined with current findings, does not support a notable etiologic role for JCV infection in colorectal cancer. (C)2014 AACR.
引用
收藏
页码:2591 / 2596
页数:6
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