Podoplanin expression in primary central nervous system germ cell tumors: a useful histological marker for the diagnosis of germinoma

被引:80
作者
Mishima, Kazuhiko
Kato, Yukinari
Kaneko, Mika K.
Nakazawa, Youya
Kunita, Akiko
Fujita, Naoya
Tsuruo, Takashi
Nishikawa, Ryo
Hirose, Takanori
Matsutani, Masao
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Saitama Med Sch, Dept Neurosurg, Moroyama, Saitama 3500495, Japan
[3] Tokyo Metropolitan Inst Neurosci, Dept Dev Neurosci, Fuchu, Tokyo 1838526, Japan
[4] Japanese Fdn Canc Res, Ctr Canc Chemotherapy, Tokyo 1358550, Japan
[5] Saitama Med Sch, Dept Pathol, Moroyama, Saitama 3500495, Japan
关键词
podoplanin; germinoma; germ cell tumor; YM-1; tumor marker;
D O I
10.1007/s00401-006-0033-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Podoplanin, a mucin-like transmembrane sialoglycoprotein, promotes platelet aggregation and may be involved in cancer cell migration, invasion, metastasis, and malignant progression. Podoplanin/aggrus is highly expressed in testicular seminoma, suggesting that it may be a sensitive marker for testicular seminomas. Here we investigated the expression of podoplanin in central nervous system (CNS) germ cell tumors (GCTs) by immunohistochemical staining of tumor samples from 62 patients. In 40 of 41 (98%) germinomas (including germinomatous components in mixed GCTs), podoplanin was diffusely expressed on the surface of germinoma cells; lymphocytes, interstitial cells, and syncytiotrophoblastic giant cells were negative for podoplanin. Except for immature teratomas (12/17; 71%), podoplanin expression was absent in non-germinomatous GCTs, including seven teratomas, seven embryonal carcinomas, seven yolk sac tumors, and seven choriocarcinomas. In immature teratomas, focal podoplanin staining was observed in fewer than 10% of immature squamous and columnar epithelial cells. Thus, podoplanin expression may be a sensitive immunohistochemical marker for germinoma in CNS GCTs. As such, it may be useful for diagnosis, for monitoring the efficacy of treatment, and as a potential target for antibody-based therapy.
引用
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页码:563 / 568
页数:6
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