首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >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
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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

机译:N-(4-甲基苯基磺酰基)-N'-(4-氯苯基)脲(LY181984)对表皮生长因子的抑制作用对NADH氧化酶活性和HeLa细胞生长的抑制作用

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摘要

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 μM. 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.
机译:从HeLa细胞分离的右侧质膜囊泡在其外表面表现出NADH氧化酶活性,该活性被抗肿瘤磺酰脲N-(4-甲基苯基磺酰基)-N'-(4-氯苯基)脲(LY181984)抑制。完整的HeLa细胞(新鲜或冷冻)在细胞外表面也显示出NADH氧化酶活性。通过添加表皮生长因子(EGF)增强了LY181984对这种活性的抑制。添加顺序至关重要。 EGF紧随LY181984之后。如果首先施用EGF,则对LY181984的反应不受EGF影响。 EGF也增强了[3H] LY181984与HeLa细胞的结合。 HeLa细胞的生长实验显示出对EGF的相似反应模式。 LY181984的生长抑制EC50为约100μM。但是,如果在LY181984之后添加10 nM EGF,则LY181984的EC50降低至约30 nM,这现在近似于先前确定的[nH] LY181984结合Kd 30 nM和EC50 30 nM对NADH的抑制作用。 LY181984通过分离的质膜囊泡产生氧化酶活性。在存在或不存在EGF的情况下,无肿瘤活性的磺酰脲类N-(甲基苯基磺酰基-N'-(苯基)脲)在抑制NADH氧化和HeLa细胞生长方面均无效。

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