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抗肿瘤药物对致癌RNA病毒逆转录酶和细胞核酸聚合酶抑制作用的碱基特异性

Base specificity in the inhibition of oncornavirus reverse transcriptase and cellular nucleic acid polymerases by antitumor drugs.

作者信息

Sethi V S

出版信息

Ann N Y Acad Sci. 1977 Mar 4;284:508-24. doi: 10.1111/j.1749-6632.1977.tb21984.x.

Abstract

Adriamycin, daunomycin, acridylmethanesulfonanilide, and alkoxybenzophenanthridine alkaloids (coralyne acetosulfate, fagaronine chloride, and nitidine chloride) inhibit template-directed nucleic acid polymerizing enzyme activities like reverse transcriptase, DNA polymerase, and RNA polymerase. Enzyme reactions with poly(dA-dT), poly(rA)-oligo(dT) and poly(dA)-oligo(dT) are more strongly inhibited by the drugs than those with poly(dC)-poly(dG) and poly(rC)-oligo(dG). These results suggest that the antitumor drugs inhibit nucleic acid polymerases by a specific interaction with A:T base pairs of the templates.

摘要

阿霉素、柔红霉素、吖啶甲磺酰苯胺以及烷氧基苯菲啶生物碱(珊瑚硫酸乙酰酯、氯化法卡林二醇和氯化两面针碱)可抑制诸如逆转录酶、DNA聚合酶和RNA聚合酶等模板导向的核酸聚合酶活性。与聚(dA-dT)、聚(rA)-寡聚(dT)和聚(dA)-寡聚(dT)的酶反应比与聚(dC)-聚(dG)和聚(rC)-寡聚(dG)的酶反应更易受到这些药物的抑制。这些结果表明,抗肿瘤药物通过与模板的A:T碱基对特异性相互作用来抑制核酸聚合酶。

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