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组蛋白去乙酰化酶抑制剂可增强HAMLET的杀肿瘤作用。

Histone deacetylase inhibitors promote the tumoricidal effect of HAMLET.

作者信息

Brest Patrick, Gustafsson Mattias, Mossberg Ann-Kristin, Gustafsson Lotta, Duringer Caroline, Hamiche Ali, Svanborg Catharina

机构信息

Institute of Laboratory Medicine, Section of Microbiology, Immunology, and Glycobiology, Lund University, Lund, Sweden.

出版信息

Cancer Res. 2007 Dec 1;67(23):11327-34. doi: 10.1158/0008-5472.CAN-07-1153.

Abstract

Histone deacetylase inhibitors (HDIs) and HAMLET (human alpha-lactalbumin made lethal to tumor cells) interact with histones, modify the structure of chromatin, and trigger tumor cell death. This study investigated how the combination of HDIs and HAMLET influences cell viability, histone acetylation, and DNA integrity. The pretreatment of tumor cells with HDIs was shown to enhance the lethal effect of HAMLET and the histone hyperacetylation response to HDIs increased even further after HAMLET treatment. HDIs and HAMLET were shown to target different histone domains as HAMLET bound tailless core histones, whereas HDIs modify the acetylation of the histone tail. DNA damage in response to HAMLET was increased by HDIs. The DNA repair response (p21WAFI expression) was induced by both agonists but abolished when the two agonists were combined. The results suggest that the synergy of HDIs and HAMLET is based on different but converging death pathways, both involving chromatin alterations. We speculate that HAMLET and HDIs might be combined to promote tumor cell death in vivo.

摘要

组蛋白去乙酰化酶抑制剂(HDIs)和HAMLET(对肿瘤细胞具有致死性的人α-乳白蛋白)与组蛋白相互作用,改变染色质结构,并引发肿瘤细胞死亡。本研究调查了HDIs与HAMLET的联合使用如何影响细胞活力、组蛋白乙酰化和DNA完整性。结果显示,用HDIs预处理肿瘤细胞可增强HAMLET的致死效应,且在HAMLET处理后,对HDIs的组蛋白高乙酰化反应进一步增强。由于HAMLET结合无尾核心组蛋白,而HDIs修饰组蛋白尾部的乙酰化,因此HDIs和HAMLET显示出靶向不同的组蛋白结构域。HDIs会增加对HAMLET产生反应的DNA损伤。两种激动剂均诱导了DNA修复反应(p21WAFI表达),但当两种激动剂联合使用时,该反应被消除。结果表明,HDIs与HAMLET的协同作用基于不同但相互汇聚的死亡途径,二者均涉及染色质改变。我们推测,HAMLET和HDIs或许可以联合使用,以促进体内肿瘤细胞死亡。

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