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一类新型抗肿瘤药物:硅氮烷衍生物对体外侵袭活性的抑制作用

Inhibition of invasion activity in vitro by a novel class of antitumor agents: silatrane derivatives.

作者信息

Grna A, Ledinko N, Fazely F, Darling S, Hogan J

机构信息

Department of Chemistry, University of Akron, Ohio 44325.

出版信息

Anticancer Res. 1988 Mar-Apr;8(2):249-53.

PMID:3364936
Abstract

The effect of several silatranes on in vitro invasion of the human amnion basement membrane (BM) by A549 human lung carcinoma cells was examined. Cells treated for two days with the derivatives were examined for invasive activity in the absence of the compounds. From silatrane dose-invasion response curves, an 80% inhibition of invasiveness compared to untreated cells was obtained with 40 micrograms/mg of 1-vinyl silatrane, 50 micrograms/ml of 1-(p-aminophenyl) silatrane, 80 micrograms/mg of 1-(3-phenylthiocarbamidopropyl) silatrane, 66 micrograms/ml of parent silatrane or 171 micrograms/ml of 1-bromosilatrane. Treatment with these doses had no effect on viability, growth or BM attachment of A549 cells.

摘要

研究了几种硅氮烷对A549人肺癌细胞体外侵袭人羊膜基底膜(BM)的影响。用这些衍生物处理细胞两天后,在无化合物的情况下检测细胞的侵袭活性。从硅氮烷剂量-侵袭反应曲线可知,与未处理细胞相比,40微克/毫克的1-乙烯基硅氮烷、50微克/毫升的1-(对氨基苯基)硅氮烷、80微克/毫克的1-(3-苯基硫脲基丙基)硅氮烷、66微克/毫升的母体硅氮烷或171微克/毫升的1-溴硅氮烷可使侵袭性抑制80%。用这些剂量处理对A549细胞的活力、生长或与基底膜的附着没有影响。

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