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蛋白激酶C抑制剂增强顺二氯二氨铂(II)和氮芥的抗增殖作用。

Enhancement of the antiproliferative effect of cis-diamminedichloroplatinum(II) and nitrogen mustard by inhibitors of protein kinase C.

作者信息

Hofmann J, Doppler W, Jakob A, Maly K, Posch L, Uberall F, Grunicke H H

机构信息

Institut für Medizinische Chemie und Biochemie, Universität Innsbruck, Austria.

出版信息

Int J Cancer. 1988 Sep 15;42(3):382-8. doi: 10.1002/ijc.2910420313.

Abstract

Quercetin (3,3',4',5,7-pentahydroxyflavone) has been shown to inhibit a variety of enzymes including the calcium- and phospholipid-dependent protein kinase (protein kinase C) in vivo and in vitro. We show that this compound synergistically enhances the antiproliferative activity of cis-diamminedichloroplatinum(II) (cis-DDP) and nitrogen mustard. Quercetin does not affect the repair of DNA interstrand cross-links introduced by cis-DDP. Long-term exposure to 12-O-tetradecanoylphorbol-13-acetate (TPA), which reduces total protein kinase C activity, also amplifies the growth-inhibitory effect of cis-DDP and acts synergistically with quercetin. A synergism is also observed if tamoxifen or staurosporine are combined with cis-DDP. For both drugs the dose-effect curves for the inhibition of protein kinase C closely resemble the dose-effect curves for the antiproliferative activities. Although alternative mechanisms cannot be definitively excluded, the effects of quercetin, TPA, tamoxifen and staurosporine may result from the inhibition of protein kinase C.

摘要

槲皮素(3,3',4',5,7 - 五羟基黄酮)已被证明在体内和体外均可抑制多种酶,包括钙和磷脂依赖性蛋白激酶(蛋白激酶C)。我们发现该化合物可协同增强顺 - 二氨二氯铂(II)(顺铂)和氮芥的抗增殖活性。槲皮素不影响顺铂引起的DNA链间交联的修复。长期暴露于12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)可降低总蛋白激酶C活性,也可增强顺铂的生长抑制作用,并与槲皮素协同发挥作用。当他莫昔芬或星形孢菌素与顺铂联合使用时也观察到协同作用。对于这两种药物,抑制蛋白激酶C的剂量效应曲线与抗增殖活性的剂量效应曲线非常相似。虽然不能完全排除其他机制,但槲皮素、TPA、他莫昔芬和星形孢菌素的作用可能是由于抑制了蛋白激酶C。

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