Suppr超能文献

含5-巯基胞嘧啶碱基的单核苷酸和多核苷酸对人癌细胞系的体外抑制作用。

Inhibition of human cancer cell lines in vitro with mono- and polynucleotides containing 5-mercaptocytosine bases.

作者信息

Geng B Q, Ho Y K, Hughes R G, Bardos T J

机构信息

Department of Medicinal Chemistry, State University of New York, Buffalo 14260.

出版信息

Zhongguo Yao Li Xue Bao. 1991 Mar;12(2):115-20.

PMID:1776473
Abstract

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.

摘要

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。

相似文献

5
Poly I-Mercapto Poly C: antiviral, anticellular, and pharmacologic effects.
Res Commun Chem Pathol Pharmacol. 1984 Sep;45(3):407-19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验