Case-control Study of Merkel Cell Polyomavirus Infection and Cutaneous Squamous Cell Carcinoma

被引:50
|
作者
Rollison, Dana E. [1 ]
Giuliano, Anna R. [1 ]
Messina, Jane L. [2 ,3 ,4 ]
Fenske, Neil A. [3 ,4 ]
Cherpelis, Basil S. [4 ]
Sondak, Vernon K. [2 ]
Roetzheim, Richard G. [5 ]
Iannacone, Michelle R. [1 ]
Michael, Kristina M. [6 ]
Gheit, Tarik [7 ]
Waterboer, Tim [6 ]
Tommasino, Massimo [7 ]
Pawlita, Michael [6 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Canc Epidemiol, Tampa, FL 33647 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Cutaneous Oncol Program, Tampa, FL 33647 USA
[3] Univ S Florida, Coll Med, Dept Pathol & Cell Biol, Tampa, FL USA
[4] Univ S Florida, Coll Med, Dept Dermatol & Cutaneous Surg, Tampa, FL USA
[5] Univ S Florida, Coll Med, Dept Family Med, Tampa, FL USA
[6] German Canc Res Ctr, Infect & Canc Program, D-69120 Heidelberg, Germany
[7] Int Agcy Res Canc, F-69372 Lyon 08, France
关键词
NONMELANOMA SKIN-CANCER; DNA; ANTIBODIES;
D O I
10.1158/1055-9965.EPI-11-0764
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Merkel cell polyomavirus (MCV) DNA has been reported in 0% to 25% of squamous cell carcinomas (SCC) occurring in immunocompetent individuals. We conducted the first serologic case-control study of MCV and SCC. Methods: Patients with histologically confirmed cutaneous SCC (n = 173) were recruited from a university dermatology clinic. Controls were individuals who screened negative for and had no history of skin or other cancers (n = 300). Levels of antibodies against capsid antigens for MCV and another polyomavirus, JC virus (JCV), were determined by fluorescent bead-based multiplex serology. Fresh-frozen tumor tissues were obtained from 145 SCC cases and tested for MCV DNA by multiplexed PCR. Associations between MCV seroreactivity and SCC were estimated by ORs and 95% CIs calculated using logistic regression with adjustment for age and sex. Results: MCV DNA was detected in SCC tumor tissues from 55 (38%) of 145 cases. A statistically significant association was observed between MCV seropositivity and MCV DNA-positive SCC (OR = 2.49, 95% CI = 1.03-6.04), with an almost four-fold association observed when comparing those with MCV antibodies in the fourth versus first quartiles (OR = 3.93, 95% CI = 1.43-10.76, P-trend = 0.01). No significant associations were observed between MCV seropositivity and MCV DNA-negative SCC (OR = 1.38, 95% CI = 0.76-2.48) or between JCV seropositivity and MCV DNA-positive or DNA-negative SCC. Conclusion: Past exposure to MCV may be a risk factor for SCC. Impact: Understanding the role of viral infections in the development of nonmelanoma skin cancer could lead to novel prevention strategies. Cancer Epidemiol Biomarkers Prev; 21(1); 74-81. (C) 2011 AACR.
引用
收藏
页码:74 / 81
页数:8
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