Expression of vascular endothelial growth factor isoforms and platelet-derived endothelial cell growth factor in bladder cancer

Citation
Nc. Li et al., Expression of vascular endothelial growth factor isoforms and platelet-derived endothelial cell growth factor in bladder cancer, UROL ONCOL, 6(1), 2001, pp. 10-15
Citations number
32
Categorie Soggetti
Urology & Nephrology
Journal title
UROLOGIC ONCOLOGY
ISSN journal
10781439 → ACNP
Volume
6
Issue
1
Year of publication
2001
Pages
10 - 15
Database
ISI
SICI code
1078-1439(200101/02)6:1<10:EOVEGF>2.0.ZU;2-R
Abstract
We analyzed the expression of vascular endothelial growth factor (VEGF) mes senger ribonucleic acid (mRNA) isoforms and platelet-derived endothelial ce ll growth factor (PDECGF) mRNA in bladder cancer. We also attempted to dete rmine if correlation exists between their expression level and conventional clinical variables in patients with bladder cancer. Tissues obtained from 60 patients with bladder carcinoma were used for analysis. Expression level s of VEGF isoforms and PDECGF were examined using reverse transcription-pol ymerase chain reaction (RT-PCR). Correlations between the expression levels of each VEGF isoform and PDECGF and histopathologic findings were evaluate d. Four VEGF isoforms corresponding to VEGF121. 165, 189. and 206 were dete cted in bladder cancer tissue by RT-PCR. Gene expression of all VEGF isofor ms as a ratio of the target to glyceraldehyde 3-phosphate dehydrogenase (GA PDH) showed no correlation with pathologic stage of bladder cancer. However , with regard to relative expression levels of VEGF isoform, which is the r atio to the sum of total VEGF isoforms. the levels of VEGF206 and VEGF189 i n tumor samples of grade pT2 or higher were significantly lower than those in tumors of grade pT1 or lower (P<.05). In contrast, the levels of VEGF121 in <greater than or equal to>pT2 tumors tended to be higher than those in less than or equal to pT1 tumors (P=.056). The expression level of PDECGF a s a ratio to GAPDH in pT2 less than or equal to tumors was significantly hi gher than that in either pTa or pT1 tumors (P<.05). Moreover. a higher expr ession level of PDECGF was observed in G3 tumors than in G1 tumors (P<.05). The results indicated that gene expression of VEGF isoforms do not play a significant role in tumor progression or invasion; however, the distributio n of VEGF isoforms may play a role in tumor progression of bladder cancer. A high expression level of PDECGF correlated significantly with the tumor p rogression of bladder cancer. (C) 2000 Elsevier Science Inc. All rights res erved.