Crew J P, O'Brien T, Bradburn M, Fuggle S, Bicknell R, Cranston D, Harris A L
Molecular Angiogenesis Group, Imperial Cancer Research Fund, The Institute of Molecular Medicine, University of Oxford, United Kingdom.
Cancer Res. 1997 Dec 1;57(23):5281-5.
Tumor development is angiogenesis dependent, and vascular endothelial growth factor (VEGF) is a key growth factor in this process. We demonstrate that high expression of VEGF mRNA in 55 superficial bladder cancers was associated with earlier recurrence (P = 0.001; hazard ratio, 3.09) and progression to a more invasive phenotype (P = 0.02; hazard ratio, 5.33). VEGF mRNA expression correlated with protein levels in superficial tumors (r = 0.59, P = 0.003) and normal bladder (r = 0.65, P < 0.05), although the ratio of VEGF protein to mRNA was elevated in tumors compared to normal bladder (P = 0.004), suggesting posttranscriptional regulation. In this study, VEGF is implicated as a major downstream mediator of the effects of the p53 tumor suppressor gene by the association between high p53 protein (determined immunochemically) and high VEGF protein and mRNA expression (P < 0.02), although in cases without high p53 protein expression, high VEGF mRNA also predicts a poor prognosis. The relationship between VEGF and early tumor recurrence suggests that seeding via angiogenesis may be a major mechanism in the pathogenesis of recurrence. These studies indicate that VEGF can predict the behavior of superficial bladder tumors and is a therapeutic target for intravesical therapy.
肿瘤的发展依赖于血管生成,而血管内皮生长因子(VEGF)是这一过程中的关键生长因子。我们证明,55例浅表性膀胱癌中VEGF mRNA的高表达与早期复发相关(P = 0.001;风险比,3.09),并进展为更具侵袭性的表型(P = 0.02;风险比,5.33)。VEGF mRNA表达与浅表肿瘤(r = 0.59,P = 0.003)和正常膀胱组织(r = 0.65,P < 0.05)中的蛋白水平相关,尽管与正常膀胱相比,肿瘤中VEGF蛋白与mRNA的比例升高(P = 0.004),提示存在转录后调控。在本研究中,通过高p53蛋白(免疫化学测定)与高VEGF蛋白和mRNA表达之间的关联(P < 0.02),VEGF被认为是p53肿瘤抑制基因作用的主要下游介质,尽管在无高p53蛋白表达的病例中,高VEGF mRNA也预示预后不良。VEGF与肿瘤早期复发之间的关系表明,通过血管生成进行播散可能是复发发病机制中的主要机制。这些研究表明,VEGF可以预测浅表性膀胱肿瘤的行为,并且是膀胱内治疗的治疗靶点。