4.7 Article

Detection of Merkel Cell Polyomavirus in Merkel Cell Carcinoma and Kaposi's Sarcoma

Journal

JOURNAL OF MEDICAL VIROLOGY
Volume 81, Issue 11, Pages 1951-1958

Publisher

WILEY
DOI: 10.1002/jmv.21608

Keywords

Merkel cell polyomavirus; Merkel cell carcinoma; real-time PCR; Kaposi's sarcoma

Categories

Funding

  1. Ministry of Health, Labor and Welfare [H21-AIDS-Ippan-006, H19-AIDS-Ippan-003, H20-Nanchi-Ippan-035, H20-Shinko-Ippan-006]
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan [21590520]
  3. Japan Health Sciences Foundation [SAA4832]
  4. Grants-in-Aid for Scientific Research [21590520] Funding Source: KAKEN

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Merkel cell carcinoma is a rare malignancy that sometimes occurs in the skin of elderly people. Recently, a new human polyomavirus, Merkel cell polyomavirus (MCPyV) was identified in Merkel cell carcinoma. In the present study, MCPyV-DNA was detected in 6 of 11 (55%) cases of Merkel cell carcinoma by nested PCR and real-time PCR. Histologically, MCPyV-positive cases showed round and vesicular nuclei with a fine granular chromatin and small nucleoli, whereas MCPyV-negative cases showed polygonal nuclei with diffusely distributed chromatin. Real-time PCR analysis to detect the MCPyV gene revealed that viral copy numbers ranged 0.04-0.43 per cell in cases of Merkel cell carcinoma. MCPyV was also detected in 3 of 49 (6.1%) cases of Kaposi's sarcoma (KS), but not in 192 DNA samples of other diseases including 142 autopsy samples from 20 immunodeficient patients. The MCPyV copy number in KS was lower than that in Merkel cell carcinoma. PCR successfully amplified a full-length MCPyV genome from a case of KS. Sequence analysis revealed that the MCPyV isolated from KS had 98% homology to the previously reported MCPyV genomes. These data suggest that the prevalence of MCPyV is low in Japan, and is at least partly associated with the pathogenesis of Merkel cell carcinoma. J. Med. Virol. 81: 1951-1958, 2009. (C) 2009 Wiley-Liss, Inc.

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