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Mol Biol Rep ; 51(1): 693, 2024 May 25.
Artigo em Inglês | MEDLINE | ID: mdl-38796656

RESUMO

BACKGROUND: Testicular germ cell tumors (TGCTs) exhibit diverse biological and pathological features and are divided in two main types, seminomas and nonseminomatous germ cell tumors (NSGCTs). CD44 is a cell surface receptor, which is highly expressed in malignancies and is implicated in tumorigenesis affecting cell-matrix interactions and cell signaling. METHODS AND RESULTS: Here, we examined the expression of CD44 in tumor cell lines and in patients' material. We found that CD44 is over-expressed in TGCTs compared to normal tissues. Immunohistochemical staining in 71 tissue specimens demonstrated increased expression of CD44 in some patients, whereas CD44 was absent in normal tissue. In seminomas, a high percentage of tumor and stromal cells showed cytoplasmic and/or cell surface staining for CD44 as well as increased staining for CD44 in the tumor stroma was found in some cases. The increased expression of CD44 either in tumor cells or in stromal components was associated with tumor size, nodal metastasis, vascular/lymphatic invasion, and disease stage only in seminomas. The increased stromal expression of CD44 in TGCTs was positively associated with angiogenesis. CONCLUSIONS: CD44 may exhibit diverse biological functions in seminomas and NSGCTs. The expression of CD44 in tumor cells as well as in tumor stroma fosters an aggressive phenotype in seminomas and should be considered in disease treatment.


Assuntos
Receptores de Hialuronatos , Seminoma , Neoplasias Testiculares , Humanos , Receptores de Hialuronatos/metabolismo , Seminoma/metabolismo , Seminoma/patologia , Seminoma/genética , Masculino , Neoplasias Testiculares/metabolismo , Neoplasias Testiculares/patologia , Adulto , Linhagem Celular Tumoral , Pessoa de Meia-Idade , Neoplasias Embrionárias de Células Germinativas/metabolismo , Neoplasias Embrionárias de Células Germinativas/patologia , Neoplasias Embrionárias de Células Germinativas/genética , Biomarcadores Tumorais/metabolismo , Regulação Neoplásica da Expressão Gênica , Imuno-Histoquímica/métodos
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