Department of Cancer Epidemiology, Moffitt Cancer Center, Tampa, Florida.
Department of Anatomic Pathology, Moffitt Cancer Center, Tampa, Florida.
Cancer Epidemiol Biomarkers Prev. 2021 Sep;30(9):1761-1764. doi: 10.1158/1055-9965.EPI-21-0332. Epub 2021 Jun 29.
A positive association between Merkel cell polyomavirus (MCPyV) infection and cutaneous squamous cell carcinoma (cuSCC) has been observed in at least one previous case-control study. To evaluate this association in a prospective context, we investigated infections with human polyomaviruses (HPyV), including MCPyV, as predictors of keratinocyte carcinomas, including cuSCC and basal cell carcinoma (BCC), among a cohort of immunocompetent individuals enrolled in the Viruses in Skin Cancer (VIRUSCAN) Study.
Associations between markers of baseline HPyV infection (serum antibodies and viral DNA in eyebrow hairs and skin swabs) and incident keratinocyte carcinomas were modeled using Cox proportional hazards regression. Proportions of baseline HPyV infections that were concordant with a subsequent tumor positive for the same HPyV type were assessed.
No significant associations were observed between baseline markers of MCPyV or other HPyV infections and cuSCC or BCC. Less than 4.5% of baseline MCPyV infections were also detected in subsequently developed keratinocyte carcinoma tumors.
HPyV infection was not a predictor of keratinocyte carcinoma risk in this prospective cohort.
Cancer-associated infections represent attractive targets for cancer prevention; however, HPyV infections have limited potential as novel targets for cuSCC prevention.
至少有一项先前的病例对照研究观察到默克尔细胞多瘤病毒(MCPyV)感染与皮肤鳞状细胞癌(cuSCC)之间存在正相关。为了在前瞻性背景下评估这种关联,我们调查了人类多瘤病毒(HPyV)感染,包括 MCPyV,作为免疫功能正常个体队列中角质细胞癌(包括 cuSCC 和基底细胞癌(BCC)的预测因子,这些个体参加了皮肤癌中的病毒(VIRUSCAN)研究。
使用 Cox 比例风险回归模型对基线 HPyV 感染标志物(眉毛头发和皮肤拭子中的血清抗体和病毒 DNA)与新发角质细胞癌之间的关联进行建模。评估与同一 HPyV 型随后肿瘤阳性相匹配的基线 HPyV 感染比例。
基线 MCPyV 或其他 HPyV 感染标志物与 cuSCC 或 BCC 之间未观察到显著关联。随后发展的角质细胞癌肿瘤中也仅检测到不到 4.5%的基线 MCPyV 感染。
在这项前瞻性队列中,HPyV 感染不是角质细胞癌风险的预测因子。
癌症相关感染是癌症预防的有吸引力的目标;然而,HPyV 感染作为 cuSCC 预防的新靶点潜力有限。