Presence of Merkel cell polyomavirus in Japanese cutaneous squamous cell carcinoma

被引:33
|
作者
Murakami, Masanao [1 ]
Imajoh, Masayuki [1 ]
Ikawa, Takuya [2 ]
Nakajima, Hideki [3 ]
Kamioka, Mikio [4 ]
Nemoto, Yuiko [1 ]
Ujihara, Takako [5 ]
Uchiyama, Jumpei [1 ]
Matsuzaki, Shigenobu [1 ]
Sano, Shigetoshi [3 ]
Daibata, Masanori [1 ]
机构
[1] Kochi Univ, Kochi Med Sch, Dept Microbiol & Infect, Nanko Ku, Kochi 7838505, Japan
[2] Kochi Univ, Grad Sch Kuroshio Sci, Div Marine Bioresource Sci, Lab Cell Struct & Funct,Nanko Ku, Kochi 7838502, Japan
[3] Kochi Univ, Kochi Med Sch, Dept Dermatol, Nanko Ku, Kochi 7838505, Japan
[4] Kochi Univ, Kochi Med Sch, Dept Lab Med, Nanko Ku, Kochi 7838505, Japan
[5] Kochi Univ, Ctr Sci Res, Nanko Ku, Kochi 7838505, Japan
关键词
Merkel cell polyomavirus (MCPyV); Squamous cell carcinoma (SCC); Skin cancer; Japanese; Patients; Epidemiology; T-ANTIGEN; INFECTION; EXPRESSION; MELANOMA; CANCER; TUMORS;
D O I
10.1016/j.jcv.2010.09.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Merkel cell polyomavirus (MCPyV) was first identified in Merkel cell carcinoma (MCC) as a new tumor virus. Studies have also reported differing frequencies of MCPyV detection in other skin cancers in western countries. Objectives: Little is known about geographical differences of MCPyV prevalence in non-MCC tumors. We examined the existence of MCPyV in non-MCC skin cancers including squamous cell carcinoma (SCC) and basal cell carcinoma (BCC) in Japanese patients. Study design: Paraffin-embedded tissues of cutaneous SCC (n = 30) and BCC (n = 10) from Japanese patients were tested for the presence of MCPyV by polymerase chain reaction (PCR) with primer sets directed against the genes encoding large-T antigen 3 (LT3) and viral protein 1 (VP1). This was followed by DNA fragment sequencing and immunohistochemistry. Results: PCR analysis targeting the LT3 gene showed that the viral sequences were found in 4 of 30 (13%) SCC cases. Nested PCR detected the VP1 region in four cases. Sequencing analysis of these PCR-amplified fragments showed a close homology to the previously published MCPyV sequences. Immunohistochemistry with the monoclonal antibody to MCPyV LT-antigen showed positive staining in 2 of 4 LT3 PCR-positive cases. On the other hand, our BCC samples were all negative for MCPyV. Conclusion: This study suggested that Japanese cutaneous SCC is infrequently associated with MCPyV. Further worldwide epidemiological surveys are warranted to determine the possible association of MCPyV with pathogenesis of non-MCC skin cancers. (C) 2010 Elsevier B.V. All rights reserved.
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收藏
页码:37 / 41
页数:5
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