| Literature DB >> 19499546 |
Masahiro Shuda1, Reety Arora, Hyun Jin Kwun, Huichen Feng, Ronit Sarid, María-Teresa Fernández-Figueras, Yanis Tolstov, Ole Gjoerup, Mahesh M Mansukhani, Steven H Swerdlow, Preet M Chaudhary, John M Kirkwood, Michael A Nalesnik, Jeffrey A Kant, Lawrence M Weiss, Patrick S Moore, Yuan Chang.
Abstract
Merkel cell polyomavirus (MCV) is a recently discovered human virus closely related to African green monkey lymphotropic polyomavirus. MCV DNA is integrated in approximately 80% of Merkel cell carcinomas (MCC), a neuroendocrine skin cancer linked to lymphoid malignancies such as chronic lymphocytic leukemia (CLL). To assess MCV infection and its association with human diseases, we developed a monoclonal antibody that specifically recognizes endogenous and transfected MCV large T (LT) antigen. We show expression of MCV LT protein localized to nuclei of tumor cells from MCC having PCR quantified MCV genome at an average of 5.2 (range 0.8-14.3) T antigen DNA copies per cell. Expression of this putative viral oncoprotein in tumor cells provides the mechanistic underpinning supporting the notion that MCV causes a subset of MCC. In contrast, although 2.2% of 325 hematolymphoid malignancies surveyed also showed evidence for MCV infection by DNA PCR, none were positive at high viral copy numbers, and none of 173 lymphoid malignancies examined on tissue microarrays expressed MCV LT protein in tumor cells. As with some of the other human polyomaviruses, lymphocytes may serve as a tissue reservoir for MCV infection, but hematolymphoid malignancies associated with MCC are unlikely to be caused by MCV. 2009 UICCEntities:
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Year: 2009 PMID: 19499546 PMCID: PMC6388400 DOI: 10.1002/ijc.24510
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396