TY - JOUR
T1 - Presence of Merkel cell polyomavirus in Japanese cutaneous squamous cell carcinoma
AU - Murakami, Masanao
AU - Imajoh, Masayuki
AU - Ikawa, Takuya
AU - Nakajima, Hideki
AU - Kamioka, Mikio
AU - Nemoto, Yuiko
AU - Ujihara, Takako
AU - Uchiyama, Jumpei
AU - Matsuzaki, Shigenobu
AU - Sano, Shigetoshi
AU - Daibata, Masanori
N1 - Funding Information:
Funding: This work was supported by the Grant-in Aid for Scientific Research from the Japanese Ministry of Education, Culture, Sports, Science and Technology; and a grant from Osaka Cancer Research Foundation to M.D. Conflict of interest: None declared. Ethical approval: This study received the approval of the ethics committee of Kochi Medical School, Kochi University.
PY - 2011/1
Y1 - 2011/1
N2 - 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.
AB - 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.
KW - Epidemiology
KW - Japanese
KW - Merkel cell polyomavirus (MCPyV)
KW - Patients
KW - Skin cancer
KW - Squamous cell carcinoma (SCC)
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U2 - 10.1016/j.jcv.2010.09.013
DO - 10.1016/j.jcv.2010.09.013
M3 - Article
C2 - 20965777
AN - SCOPUS:78650941785
SN - 1386-6532
VL - 50
SP - 37
EP - 41
JO - Journal of Clinical Virology
JF - Journal of Clinical Virology
IS - 1
ER -