Pigment epithelium-derived factor expression is down-regulated in bladder tumors and correlates with vascular endothelial growth factor and matrix metalloproteinase-9 |
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Authors: | Chen-chen Feng Qiang Ding Yuan-fang Zhang Hao-wen Jiang Hui Wen Pao-hsun Wang Zhong Wu |
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Affiliation: | (1) Department of Urology, Huashan Hospital, Fudan University, 12 Central Urumqi Rd, Shanghai, 200040, People’s Republic of China;(2) Institute of Urology, Huashan Hospital, Fudan University, Shanghai, 200040, People’s Republic of China;(3) Department of Surgery, Huashan Hospital, Fudan University, Shanghai, 200040, People’s Republic of China; |
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Abstract: | ![]() Growth of solid tumor depends on angiogenesis, a process regulated by the balance of pro- and anti-angiogenic factors. We investigated the expression of anti-angiogenic factor pigment epithelium-derived factor (PEDF) and proangiogenic factors vascular endothelial growth factor (VEGF) and matrix metalloproteinase-9 (MMP-9) with immunohistochemistry in 64 bladder tumor samples and 23 normal controls. Compared with normal urothelium, we identified decreased PEDF expression (P = 0.000) whereas increased expression of VEGF (P = 0.000) and MMP-9 (P = 0.000) in tumorous tissue as well as in papillary urothelial neoplasm of low malignant potential (PUNLMP) (P = 0.009 and P = 0.000 accordingly) but MMP-9 (P = 0.704). Decreased PEDF expression was revealed with higher tumor grade (P = 0.014) but stage (P = 0.687). There was no age or gender preference in PEDF, VEGF or MMP-9 expression. Negative correlation of expression in tumorous and cancerous tissue regarding PEDF and VEGF (P = 0.000, r = −0.56, and P = 0.000, r = −0.50, respectively), PEDF and MMP-9 (P = 0.002, r = −0.39, and P = 0.032, r = −0.30, respectively) was identified. There was a negative correlation of expression between PEDF and VEGF (P = 0.016, r = −0.677) and no correlation between PEDF and MMP-9 (P = 0.147, r = −0.45) in PUNLMP. Decreased PEDF and increased VEGF and MMP-9 expression may play considerable roles in differentiation and invasion of bladder tumor. |
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