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Expression of Platelet‐derived Endothelial Cell Growth Factor/Thymidine Phosphorylase in Human Bladder Cancer

We investigated the expression of platelet‐derived endothelial cell growth factor/thymidine phosphorylase (PD‐ECGF/TP) in primary bladder cancer, its association with clinicopathologic findings, and their prognostic value. mRNA was extracted from 20 bladder cancer specimens and 6 normal bladder muco...

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Detalles Bibliográficos
Autores principales: Tanaka, Tsutomu, Yoshiki, Tatsuhiro, Arai, Yoichi, Higuchi, Kayoko, Kageyama, Susumu, Ogawa, Yasutaka, Isono, Takahiro, Okada, Yusaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926031/
https://www.ncbi.nlm.nih.gov/pubmed/10665652
http://dx.doi.org/10.1111/j.1349-7006.1999.tb00718.x
Descripción
Sumario:We investigated the expression of platelet‐derived endothelial cell growth factor/thymidine phosphorylase (PD‐ECGF/TP) in primary bladder cancer, its association with clinicopathologic findings, and their prognostic value. mRNA was extracted from 20 bladder cancer specimens and 6 normal bladder mucosal tissues. Relative amounts of PD‐ECGF/TP mRNA were evaluated by reverse transcriptase‐polymerase chain reaction (RT‐PCR) and compared with the level of glycer‐aldehyde‐3‐phosphate dehydrogenase mRNA (used as an internal standard). PD‐ECGF/TP expression was examined by immunohistochemistry in 85 patients who underwent cystectomy for bladder cancer. Serum PD‐ECGF/TP levels were measured in 23 patients using a sandwich‐type enzyme‐linked immunosorbent assay. By RT‐PCR analysis, expression of PD‐ECGF/TP was found to be 7‐fold higher in invasive tumors than in superficial tumors (P<0.01) and 9‐fold higher than in normal bladder (P<0.01). Out of 85 transitional cell carcinoma tissue samples, 69 (81%) were evaluated as PD‐ECGF/TP‐positive by immunohistochemical staining. PD‐ECGF/TP expression correlated significantly with tumor grade (P=0.001), depth of invasion (P=0.012), and lymphatic invasion (P=0.01). No correlation was found between expression of PD‐ECGF/TP and the number of tumors, tumor configuration, lymph node involvement, venous invasion, c‐erbB‐2 expression, or overall survival. We could not detect a significant serum level of PD‐ECGF/TP in any patient. The results suggest that PD‐ECGF/TP might give valuable information for bladder cancer management, though it may not be a good new tumor marker for bladder cancer.