Qiu C, Ouyang Q
Department of Internal Medicine. First Hospital, West China University of Medical Sciences, Chengdu 610041, China.
Zhonghua Nei Ke Za Zhi. 2001 Jun;40(6):377-80.
To investigate the mechanism of COX-2's selective inhibitor, NS-398, on human colorectal adenoma development.
The human colorectal adenoma cells were isolated and cultured identified. The cell growth rates were assessed, when treated with NS-398, by using MTT method. Expression of COX-2 protein in human colorectal tumor was examined by immunohistochemistry.
23 of 30 colorectal adenomas were primary cultured successfully. NS-398 inhibited the proliferation of the cells in a dose- and time-dependent manner. COX-2 was overexpressed in colorectal adenoma(83.1%) and cancer(80.0%)compared with normal colon mucosa.
The key of the several culture conditions for the survival of human colorectal adenoma cells have been improved. Such as, best of the digestive time and number of cell. The cells can be inhibited by NS-398 with dose-dependent. Overexpression of COX-2 protein occurs early during colorectal carcinogenesis which contribute to tumour formation.
探讨环氧化酶-2(COX-2)选择性抑制剂NS-398对人结肠腺瘤发生发展的作用机制。
分离培养人结肠腺瘤细胞并进行鉴定。采用MTT法评估NS-398处理后人结肠腺瘤细胞的生长速率。采用免疫组织化学法检测人结肠肿瘤组织中COX-2蛋白的表达。
30例结肠腺瘤中有23例原代培养成功。NS-398以剂量和时间依赖的方式抑制细胞增殖。与正常结肠黏膜相比,COX-2在结肠腺瘤(83.1%)和结肠癌(80.0%)中高表达。
优化了人结肠腺瘤细胞存活的几种培养条件,如最佳消化时间和细胞数量。NS-398可剂量依赖性地抑制细胞。COX-2蛋白在结直肠癌发生早期即高表达,促进肿瘤形成。