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组蛋白去乙酰化酶抑制剂和萝卜菌素对肿瘤细胞的形态逆转作用

[Morphological reversion of tumor cells by histone deacetylase inhibitors and radicicol].

作者信息

Yoshida M, Honda A, Horinouchi S

机构信息

Dept. of Biotechnology, Graduate School of Agriculture and Life Sciences, Tokyo University.

出版信息

Gan To Kagaku Ryoho. 1997 Sep;24(11):1512-8.

PMID:9309149
Abstract

Trichostatins and trapoxins, structurally unrelated microbial metabolites, are specific inhibitors of histone deacetylases. Radicicol inhibits Src family protein-tyrosine kinases. Recently, these agents were found to induce morphological reversion and enhanced expression of gelsolin, an actin regulatory protein, in a variety of transformed cells. Microinjection of an anti-gelsolin antibody that neutralizes the gelsolin function caused inhibition of the morphological change, suggesting that gelsolin expression is associated with the suppression of transformation.

摘要

曲古抑菌素和陷阱霉素是结构不相关的微生物代谢产物,是组蛋白脱乙酰酶的特异性抑制剂。雷地昔尔抑制Src家族蛋白酪氨酸激酶。最近,发现这些药物能诱导多种转化细胞发生形态逆转,并增强肌动蛋白调节蛋白凝溶胶蛋白的表达。显微注射一种中和凝溶胶蛋白功能的抗凝溶胶蛋白抗体可抑制形态变化,这表明凝溶胶蛋白的表达与转化抑制有关。

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