Xiang Yang, Ma Bing, Li Tao, Gao Jun-Wei, Yu He-Ming, Li Xue-Jun
Department of Pharmacology, School of Basic Medical Sciences, Peking University, Beijing 100083, China.
Acta Pharmacol Sin. 2004 Jun;25(6):812-6.
To study effects of acetazolamide on aquaporin-1 (AQP(1)) protein expression and angiogenesis.
Establishing Lewis-lung-carcinoma model, the localization of AQP(1) in tumor tissues was investigated by immunohistochemical methods; The biological activity of acetazolamide was detected by endothelial cells proliferation test (MTT) assay and chorioallantoic membrane (CAM) vascular inhibition test.
Immunohistochemical localization of AQP(1) in mice tumor was labeled in capillaries, post capillary venules endothelial cells. After being treated with acetazolamide, the number of capillaries and post capillary venules was significantly decreased in tumor tissue. Acetazolamide showed significant inhibitory effect on angiogenesis in CAM and endothelial cell proliferation.
Acetazolamide might be identified and developed as one of potential lead compounds for a new therapeutic intervention in inhibiting cancer angiogenesis.
研究乙酰唑胺对水通道蛋白-1(AQP(1))蛋白表达及血管生成的影响。
建立Lewis肺癌模型,采用免疫组化方法研究AQP(1)在肿瘤组织中的定位;通过内皮细胞增殖试验(MTT)和鸡胚绒毛尿囊膜(CAM)血管抑制试验检测乙酰唑胺的生物学活性。
免疫组化显示小鼠肿瘤中AQP(1)定位于毛细血管、毛细血管后微静脉内皮细胞。乙酰唑胺处理后,肿瘤组织中毛细血管和毛细血管后微静脉数量显著减少。乙酰唑胺对CAM血管生成和内皮细胞增殖具有显著抑制作用。
乙酰唑胺可能被识别并开发为一种潜在的先导化合物,用于癌症血管生成抑制的新治疗干预。