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丁酸盐对GADD153的上调作用:丝裂原活化蛋白激酶的参与

Upregulation of GADD153 by butyrate: involvement of MAPK.

作者信息

Scott David W, Longpre Jennifer M, Loo George

机构信息

Department of Nutrition, Cellular and Molecular Nutrition Research Laboratory, University of North Carolina at Greensboro, Greensboro, North Carolina 27402-6170, USA.

出版信息

DNA Cell Biol. 2008 Nov;27(11):607-14. doi: 10.1089/dna.2008.0773.

Abstract

Butyrate inhibits the proliferation of cancer cells, but the early molecular events initiated by butyrate have not been fully identified. Herein, butyrate is shown to affect the growth arrest and DNA damage-inducible gene 153 (GADD153) in HCT-116 human colon adenocarcinoma cells. Despite absence of any detectable cellular DNA damage, the expression of GADD153 was upregulated before several features characteristic of apoptosis appeared. Butyrate-induced upregulation of GADD153 mRNA was attenuated by actinomycin D, but apparently not by cycloheximide. In investigating possible involvement of MAPK in mediating the effect of butyrate on GADD153 mRNA expression, the extracellular regulated kinase (ERK) inhibitor PD98059, but neither the JNK inhibitor SP600125 nor the p38 MAPK inhibitor SB203580, blunted the ability of butyrate to upregulate GADD153 mRNA expression. U0126, a selective inhibitor of upstream MEK, had a similar effect as PD98059 on butyrate-induced GADD153 mRNA upregulation. Collectively, these findings suggest that butyrate caused activation of the GADD153 gene at the level of transcription involving mainly the MEK/ERK branch of the MAPK signal transduction pathway. Moreover, these molecular events were not the result of any DNA damage and occurred before several features characteristic of apoptosis became evident.

摘要

丁酸盐可抑制癌细胞增殖,但丁酸盐引发的早期分子事件尚未完全明确。在此研究中,丁酸盐被证明可影响人结肠腺癌细胞HCT - 116中的生长停滞和DNA损伤诱导基因153(GADD153)。尽管未检测到任何可察觉的细胞DNA损伤,但在凋亡的几个特征出现之前,GADD153的表达就已上调。丁酸盐诱导的GADD153 mRNA上调被放线菌素D减弱,但显然不受环己酰亚胺的影响。在研究丝裂原活化蛋白激酶(MAPK)可能参与介导丁酸盐对GADD153 mRNA表达的作用时,细胞外调节激酶(ERK)抑制剂PD98059可减弱丁酸盐上调GADD153 mRNA表达的能力,而JNK抑制剂SP600125和p38 MAPK抑制剂SB203580则无此作用。上游MEK的选择性抑制剂U0126对丁酸盐诱导的GADD153 mRNA上调具有与PD98059类似的作用。总体而言,这些发现表明丁酸盐在转录水平上导致GADD153基因激活,主要涉及MAPK信号转导途径的MEK/ERK分支。此外,这些分子事件并非任何DNA损伤的结果,且在凋亡的几个特征变得明显之前就已发生。

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