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Expression of human chorionic gonadotropin in testicular germ cell tumors.
Lempiäinen, Anna; Sankila, Anna; Hotakainen, Kristina; Haglund, Caj; Blomqvist, Carl; Stenman, Ulf-Håkan.
Afiliação
  • Lempiäinen A; Department of Clinical Chemistry, Helsinki University Central Hospital Laboratory Division (HUSLAB) and Helsinki University, Helsinki, Finland. Electronic address: anna.lempiainen@helsinki.fi.
  • Sankila A; Department of Pathology, Helsinki University Central Hospital Laboratory Division (HUSLAB), Helsinki, Finland.
  • Hotakainen K; Department of Clinical Chemistry, Helsinki University Central Hospital Laboratory Division (HUSLAB) and Helsinki University, Helsinki, Finland.
  • Haglund C; Department of Surgery, Helsinki University Central Hospital and Helsinki University, Helsinki, Finland.
  • Blomqvist C; Department of Oncology, Helsinki University Central Hospital and Helsinki University, Helsinki, Finland.
  • Stenman UH; Department of Clinical Chemistry, Helsinki University Central Hospital Laboratory Division (HUSLAB) and Helsinki University, Helsinki, Finland.
Urol Oncol ; 32(5): 727-34, 2014 Jul.
Article em En | MEDLINE | ID: mdl-24502963
BACKGROUND: We have shown that most patients with seminomas have elevated serum concentrations of the free ß subunit of human chorionic gonadotropin (hCGß) and that in nonseminomatous testicular cancer, most of the hCG in the serum is hyperglycosylated (hCG-h). However, the tissue expression of hCG-h or hCGß in germ cell tumors (GCTs) has not been reported. Our objective was to study the expression and diagnostic value of hCG-h and hCGß in testicular GCTs. METHODS: We studied the immunohistochemical expression of hCG, hCG-h, hCGß, and the free α subunit of hCG (hCGα) in GCTs from 154 patients. We compared the tissue expression with serum concentrations and evaluated the correlation between staining intensity, established prognostic variables, and outcome. RESULTS: The expression varied between tumor types. All forms of hCG, including hCG-h, were detected in embryonal carcinomas (22%) and mixed GCTs (48%). Polyclonal hCG and monoclonal hCGß antibodies detected immunoreactivity in some seminomas (7%). No form of hCG was found in spermatocytic seminomas, pure teratomas, or a yolk sac tumor. The serum concentrations correlated with the corresponding tumor expression. The staining intensities of hCG, hCGß, hCG-h, and hCGα correlated with disease stage but not significantly with relapse, disease-related mortality, or progression-free survival. CONCLUSION: Trophoblastic tissue expresses hCG, hCG-h, and free subunits together whereas seminoma tissue occasionally expresses hCGß. This difference might aid in differential diagnosis of some difficult-to-classify cases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Regulação Neoplásica da Expressão Gênica / Neoplasias Embrionárias de Células Germinativas / Gonadotropina Coriônica Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Regulação Neoplásica da Expressão Gênica / Neoplasias Embrionárias de Células Germinativas / Gonadotropina Coriônica Tipo de estudo: Prognostic_studies Limite: Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article