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亚苄基内酰胺化合物KNK437,一种新型的人结肠癌细胞耐热性获得和热休克蛋白诱导抑制剂。

Benzylidene lactam compound, KNK437, a novel inhibitor of acquisition of thermotolerance and heat shock protein induction in human colon carcinoma cells.

作者信息

Yokota S, Kitahara M, Nagata K

机构信息

Takasago Research Laboratories, Research Institute, Kaneka Corporation, Japan.

出版信息

Cancer Res. 2000 Jun 1;60(11):2942-8.

Abstract

Cells exposed to heat or other types of stressors transiently synthesize a group of proteins known as heat shock proteins (HSPs). A nonlethal heat treatment can elicit in the cells an ability to resist subsequent lethal heat treatments. We report here that a novel benzylidene lactam compound, KNK437, dose-dependently inhibited the acquisition of thermotolerance and the induction of various HSPs including HSP105, HSP70, and HSP40 in COLO 320DM (human colon carcinoma) cells. The induction of heat-inducible HSP70, which is reported to be involved in the development of thermotolerance, was inhibited at mRNA levels by treatment with KNK437. This compound also inhibited the acquisition of thermotolerance as developed by sodium arsenite. However, it did not increase thermosensitivity in nontolerant cells. The effect of KNK437 was much greater than that of quercetin, a bioflavonoid that was previously reported to inhibit the acquisition of thermotolerance as well as the induction of HSPs. We conclude that this drug is a novel inhibitor of the acquisition of thermotolerance caused by the induction of HSPs.

摘要

暴露于热或其他类型应激源的细胞会短暂合成一组被称为热休克蛋白(HSPs)的蛋白质。非致死性热处理可使细胞产生抵抗后续致死性热处理的能力。我们在此报告,一种新型亚苄基内酰胺化合物KNK437,在COLO 320DM(人结肠癌细胞)中剂量依赖性地抑制耐热性的获得以及包括HSP105、HSP70和HSP40在内的各种热休克蛋白的诱导。据报道参与耐热性发展的热诱导型HSP70的诱导在mRNA水平上被KNK437处理所抑制。该化合物也抑制了由亚砷酸钠产生的耐热性的获得。然而,它并未增加非耐受细胞的热敏感性。KNK437的作用远大于槲皮素,槲皮素是一种先前报道可抑制耐热性获得以及热休克蛋白诱导的生物类黄酮。我们得出结论,该药物是一种由热休克蛋白诱导引起的耐热性获得的新型抑制剂。

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