The prevalence of Merkel cell polyomavirus in Japanese patients with Merkel cell carcinoma

被引:29
|
作者
Hattori, Tomoyasu [1 ]
Takeuchi, Yuko [1 ]
Takenouchi, Tatsuya [2 ]
Hirofuji, Akiko [3 ]
Tsuchida, Tetsuya [3 ]
Kabumoto, Takenori [4 ]
Fujiwara, Hiroshi [4 ]
Ito, Masaaki [4 ]
Shimizu, Akira [1 ]
Okada, Etsuko [1 ]
Motegi, Sei-ichiro [1 ]
Tamura, Atsushi [1 ]
Ishikawa, Osamu [1 ]
机构
[1] Gunma Univ, Dept Dermatol, Grad Sch Med, Maebashi, Gunma 3718511, Japan
[2] Niigata Canc Ctr Hosp, Div Dermatol, Niigata, Japan
[3] Saitama Med Univ, Dept Dermatol, Saitama, Japan
[4] Niigata Univ, Div Dermatol, Grad Sch Med & Dent Sci, Niigata, Japan
关键词
Merkel cell carcinoma; Merkel cell polyomavirus; Basal cell carcinoma; Squamous cell carcinoma; T-ANTIGEN; INFECTION; SKIN; PATHOGENESIS; EXPRESSION; ASSOCIATION; INTEGRATION; MCV; DNA;
D O I
10.1016/j.jdermsci.2013.02.010
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: A novel polyomavirus, the Merkel cell polyomavirus (MCPyV) has been implicated in the pathogenesis of Merkel cell carcinoma (MCC); however, the prevalence of MCPyV in Japan has not been extensively investigated. Objective: To clarify the prevalence of MCPyV in Japanese patients with MCC. Methods: MCPyV DNA was examined by polymerase chain reaction (PCR) in formalin-fixed paraffin-embedded (FFPE) or frozen tissue samples from 26 patients with MCC diagnosed in four medical centers in Japan. Immunohistochemistry was simultaneously performed using a monoclonal antibody against the viral large T (LT) antigen. FFPE samples from basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) were also analyzed as controls. Results: Twenty-three out of 26 cases (88.5%) were positive for MCPyV DNA by PCR. The amplified products harbored 4 patterns of mutations. Phylogenetic analysis demonstrated that one of our strains was closely related to the other Japanese strains previously reported. The LT antigen was expressed in various degrees in 20 of 26 cases (76.9%) by immunohistochemistry. Histological type had little relation to CM2B4 positivity, whereas 3 of 5 trabecular-type tumors showed no staining. The immunoreactivity for CM2B4 did not correlate with the relative viral DNA load. In BCC and SCC, the LT antigen was immunohistochemically positive, but MCPyV DNA was not detected by PCR. The cells around some MCC and non-MCC tumors were stained with CM2B4 with a distribution similar to CD20- and CD45RO-(especially CD8-) positive lymphocytes. Conclusion: MCPyV was highly positive in Japanese patients with MCC. It is of note that the positive rate differs depending upon the detection method. (C) 2013 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:99 / 107
页数:9
相关论文
共 50 条
  • [31] Merkel Cell Polyomavirus DNA in Persons without Merkel Cell Carcinoma
    Wieland, Ulrike
    Mauch, Cornelia
    Kreuter, Alexander
    Krieg, Thomas
    Pfister, Herbert
    EMERGING INFECTIOUS DISEASES, 2009, 15 (09) : 1496 - 1498
  • [32] Detection of the Merkel cell polyomavirus (MCV) DNA in tumor samples of Merkel cell carcinoma patients
    Varga, E.
    Kiss, M.
    Szabo, K.
    Kemeny, L.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 : S74 - S74
  • [33] Unusually young Merkel cell carcinoma patients are Merkel cell polyomavirus positive and frequently immunocompromised
    Sahi H.
    Kukko H.
    Böhling T.
    Tukiainen E.
    Sihto H.
    Joensuu H.
    Koljonen V.
    European Journal of Plastic Surgery, 2010, 33 (6) : 349 - 353
  • [34] Observation: A case of Merkel cell carcinoma infected by Merkel cell polyomavirus DNA
    Ramirez-Fort, Marigdalia
    Khan, Farhan
    Nguyen, Harrison
    Kauffman, Julia
    Rady, Peter
    Rapini, Ronald
    Tyring, Stephen
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2013, 68 (04) : AB131 - AB131
  • [35] Genomic Characterization of Merkel Cell Polyomavirus Integration Sites in Merkel Cell Carcinoma
    Duncavage, E. J.
    Demeter, R.
    Wylie, T.
    Magrini, V.
    Pfeifer, J.
    MODERN PATHOLOGY, 2012, 25 : 119A - 119A
  • [36] Clinical Factors Associated With Merkel Cell Polyomavirus Infection in Merkel Cell Carcinoma
    Sihto, Harri
    Kukko, Heli
    Koljonen, Virve
    Sankila, Risto
    Bohling, Tom
    Joensuu, Heikki
    JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2009, 101 (13): : 938 - 945
  • [37] Detection of the Merkel cell polyomavirus in the neuroendocrine component of combined Merkel cell carcinoma
    Thibault Kervarrec
    Mahtab Samimi
    Pauline Gaboriaud
    Tarik Gheit
    Agnès Beby-Defaux
    Roland Houben
    David Schrama
    Gaëlle Fromont
    Massimo Tommasino
    Yannick Le Corre
    Eva Hainaut-Wierzbicka
    Francois Aubin
    Guido Bens
    Hervé Maillard
    Adeline Furudoï
    Patrick Michenet
    Antoine Touzé
    Serge Guyétant
    Virchows Archiv, 2018, 472 : 825 - 837
  • [38] Association of merkel cell polyomavirus infection with morphologic differences in merkel cell carcinoma
    Kuwamoto, Satoshi
    Higaki, Hiromi
    Kanai, Kyosuke
    Iwasaki, Takeshi
    Sano, Hitoshi
    Nagata, Keiko
    Kato, Kaoru
    Kato, Masako
    Murakami, Ichiro
    Horie, Yasushi
    Yamamoto, Osamu
    Hayashi, Kazuhiko
    HUMAN PATHOLOGY, 2011, 42 (05) : 632 - 640
  • [39] Lack of evidence for basal or squamous cell carcinoma infection with Merkel cell polyomavirus in immunocompetent patients with Merkel cell carcinoma
    Reisinger, Diane M.
    Shiffer, Jeffrey D.
    Cognetta, Armand B., Jr.
    Chang, Yuan
    Moore, Patrick S.
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2010, 63 (03) : 400 - 403
  • [40] Merkel Cell Polyomavirus Status Is Not Associated with Clinical Course of Merkel Cell Carcinoma
    Schrama, David
    Peitsch, Wiebke K.
    Zapatka, Marc
    Kneitz, Hermann
    Houben, Roland
    Eib, Steffi
    Haferkamp, Sebastian
    Moore, Patrick S.
    Shuda, Masahiro
    Thompson, John F.
    Trefzer, Uwe
    Pfoehler, Claudia
    Scolyer, Richard A.
    Becker, Juergen C.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2011, 131 (08) : 1631 - 1638