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抗肿瘤磺酰脲类药物N-(4-甲基苯基磺酰基)-N'-(4-氯苯基)脲(LY181984)对HeLa细胞NADH氧化酶活性和生长的抑制作用以及对表皮生长因子的反应

Inhibition of NADH oxidase activity and growth of HeLa cells by the antitumor sulfonylurea, N-(4-methylphenylsulfonyl)-N'-(4-chlorophenyl) urea (LY181984) and response to epidermal growth factor.

作者信息

Morré D J, Wu L Y, Morré D M

机构信息

Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907, USA.

出版信息

Biochim Biophys Acta. 1997 Feb 4;1355(2):114-20. doi: 10.1016/s0167-4889(96)00128-0.

Abstract

Right side-out plasma membrane vesicles isolated from HeLa cells exhibited an NADH oxidase activity at their external surfaces that was inhibited by the antitumor sulfonylurea, N-(4-methylphenylsulfonyl)-N'-(4-chlorophenyl)urea (LY181984). Intact HeLa cells (fresh or frozen) also exhibited an NADH oxidase activity at the external cell surface. The inhibition of this activity by LY181984 was enhanced by the addition of epidermal growth factor (EGF). The order of addition was critical. It was necessary that the LY181984 be followed by the EGF. If the EGF was administered first, the response to LY181984 was unaffected by EGF. Binding of [3H]LY181984 to HeLa cells also was enhanced by EGF. Growth experiments with HeLa cells revealed a similar pattern of response to EGF. The EC50 of growth inhibition of LY181984 was about 100 microM. However, if the LY181984 was followed by addition of 10 nM EGF, the EC50 for LY181984 was reduced to about 30 nM which now approximated the previously determined Kd of [3H]LY181984 binding of 30 nM and the EC50 of 30 nM for inhibition of NADH oxidase activity by LY181984 by isolated vesicles of plasma membranes. The tumor-inactive sulfonylurea N-(methylphenylsulfonyl-N'-(phenyl)urea (LY181985) was ineffective in the inhibition of NADH oxidation and of growth with HeLa cells either in the presence or absence of EGF.

摘要

从HeLa细胞中分离出的外翻式质膜囊泡在其外表面表现出NADH氧化酶活性,该活性受到抗肿瘤磺酰脲类药物N-(4-甲基苯基磺酰基)-N'-(4-氯苯基)脲(LY181984)的抑制。完整的HeLa细胞(新鲜的或冷冻的)在外细胞表面也表现出NADH氧化酶活性。表皮生长因子(EGF)的添加增强了LY181984对该活性的抑制作用。添加顺序至关重要。必须先加入LY181984,然后再加入EGF。如果先施用EGF,对LY181984的反应不受EGF影响。[3H]LY181984与HeLa细胞的结合也因EGF而增强。HeLa细胞的生长实验显示出对EGF的类似反应模式。LY181984生长抑制的EC50约为100 microM。然而,如果在LY181984之后加入10 nM EGF,LY181984的EC50会降至约30 nM,这现在接近先前测定的[3H]LY181984结合的Kd值30 nM以及LY181984对分离的质膜囊泡NADH氧化酶活性抑制的EC50值30 nM。肿瘤无活性的磺酰脲类药物N-(甲基苯基磺酰基-N'-(苯基)脲(LY181985)在有或没有EGF的情况下,对HeLa细胞的NADH氧化和生长抑制均无效。

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