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Depression of histone acetylation by alkylating antitumor agents in murine cells.

作者信息

Zwierzina H, Loidl A, Fuith L C, Helliger W, Puschendorf B, Grunicke H

出版信息

Cancer Res. 1984 Aug;44(8):3336-9.

PMID:6744267
Abstract

Treatment of Ehrlich ascites tumor cells with the alkylating agent triaziquone [2,3,5-tris(ethyleneimino)benzoquinone-1,4] and nitrogen mustard leads to a reduction of the posttranslational acetylation of histones. Acetylation of all core histones is affected. The reduction of labeling of acetylated sites is accompanied by a dose-dependent decrease in the extent of acetylation as indicated by the level of acetylation of H4. The depression of histone acetylation is expressed at all concentrations of the alkylating agents which cause significant inhibition of tumor cell proliferation. It could be excluded that the observed effects are caused by an impairment of acetyl coenzyme A synthesis.

摘要

相似文献

1
Depression of histone acetylation by alkylating antitumor agents in murine cells.
Cancer Res. 1984 Aug;44(8):3336-9.
2
Depression of histone acetylation by alkylating antitumor agents: significance for antitumor activity and possible biological consequences.烷基化抗肿瘤药物对组蛋白乙酰化的抑制作用:对抗肿瘤活性的意义及可能的生物学后果。
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3
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[Unfolding of nucleosome cores induced by chemical acetylation of histones].[组蛋白化学乙酰化诱导核小体核心解折叠]
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YM753, a novel histone deacetylase inhibitor, exhibits antitumor activity with selective, sustained accumulation of acetylated histones in tumors in the WiDr xenograft model.YM753是一种新型组蛋白去乙酰化酶抑制剂,在WiDr异种移植模型中,它通过在肿瘤中选择性、持续地积累乙酰化组蛋白而表现出抗肿瘤活性。
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引用本文的文献

1
Postsynthetic acetylation of histones during the cell cycle: a general function for the displacement of histones during chromatin rearrangements.细胞周期中组蛋白的合成后乙酰化:染色质重排过程中组蛋白置换的一般功能。
Nucleic Acids Res. 1987 Oct 26;15(20):8351-66. doi: 10.1093/nar/15.20.8351.