Miura T, Kubota Y, Sakuramoto T, Hosaka M
Department of Urology, Yokahama City University, School of Medicine, Japan.
Urol Res. 1987;15(4):187-90. doi: 10.1007/BF00262096.
An in vitro chemosensitivity test was applied to clinical specimens of urogenital cancer tissues obtained at operation. Incorporation of 3H-leucine into primary cultured cells 24 h after treatment with cytotoxic drugs was used as an index for cell viability. Primary cell culture was performed using specimens obtained from 37 patients including 20 with transitional cell carcinoma, 15 with renal cell carcinoma and 2 with testicular cancer. Primary cell growth was achieved in 27 (73%) out of 37 specimens and 10 were tested for chemosensitivity. Each specimen of the tumor revealed different sensitivity to drugs, and results of quadruplicate tests for each specimen were identical. It was concluded that the present method of measuring incorporation of radioactivity using urogenital cancer cells primarily cultured in microtiter plate is practically applicable to an in vitro chemosensitivity test.
对手术获取的泌尿生殖系统癌组织临床标本进行了体外化学敏感性试验。用细胞毒性药物处理24小时后,将3H-亮氨酸掺入原代培养细胞中的情况用作细胞活力指标。使用从37例患者获取的标本进行原代细胞培养,其中包括20例移行细胞癌、15例肾细胞癌和2例睾丸癌患者。37个标本中有27个(73%)实现了原代细胞生长,对其中10个进行了化学敏感性测试。每个肿瘤标本对药物显示出不同的敏感性,每个标本的四次重复测试结果均相同。得出结论,目前使用在微量滴定板中原代培养的泌尿生殖系统癌细胞测量放射性掺入的方法实际上适用于体外化学敏感性试验。