Geng B Q, Ho Y K, Hughes R G, Bardos T J
Department of Medicinal Chemistry, State University of New York, Buffalo 14260.
Zhongguo Yao Li Xue Bao. 1991 Mar;12(2):115-20.
Partially thiolated polycytidylic acid (5-mercaptopolycytidylic, MPC) and its double-stranded complex with polyinosinic acid [poly (I)].poly(I).MPC, were assayed in both antiproliferative and cytotoxicity tests against human cell lines: lung carcinoma A549, colon carcinoma HT-29, osteosarcoma HOS, and amnion cells (WISH). Inhibitory effects of MPC were noted in the antiproliferative assay with ID50 of 7, 24, 33, and 35 micrograms.ml-1, and in the cytotoxicity test with ID50 of 164, 174, 210, and 290 micrograms.ml-1 against the HOS, A549, HT-29, and WISH cells respectively. Comparison with the corresponding partially thiolated mononucleotide (5-mercapto-CMP + CMP) and the nucleoside (5-mercapto-cytidine) demonstrated that MPC was a more potent antiproliferative agent than either of its monomeric constituents. The inhibitory effect of MPC upon the incorporation of [3H]thymidine into the DNA of growing A549 cells paralleled its antiproliferative activity.
对部分硫醇化的聚胞苷酸(5-巯基聚胞苷酸,MPC)及其与聚肌苷酸的双链复合物[聚(I)]·聚(I)·MPC,进行了针对人细胞系的抗增殖和细胞毒性测试:肺癌A549细胞系、结肠癌HT-29细胞系、骨肉瘤HOS细胞系和羊膜细胞(WISH)。在抗增殖试验中,观察到MPC的抑制作用,对HOS、A549、HT-29和WISH细胞的半数抑制浓度(ID50)分别为7、24、33和35微克·毫升-1;在细胞毒性试验中,其ID50分别为164、174、210和290微克·毫升-1。与相应的部分硫醇化单核苷酸(5-巯基胞苷酸+胞苷酸)和核苷(5-巯基胞苷)相比,结果表明MPC是一种比其任何一种单体成分更有效的抗增殖剂。MPC对生长中的A549细胞DNA中[3H]胸腺嘧啶核苷掺入的抑制作用与其抗增殖活性平行。