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组蛋白去乙酰化酶抑制剂曲古抑菌素A和丙戊酸可诱导永生化人子宫内膜基质细胞发生细胞周期阻滞并表达p21。

Histone deacetylase inhibitors trichostatin A and valproic acid induce cell cycle arrest and p21 expression in immortalized human endometrial stromal cells.

作者信息

Wu Yan, Guo Sun-Wei

机构信息

Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2008 Apr;137(2):198-203. doi: 10.1016/j.ejogrb.2007.02.014. Epub 2007 Mar 21.

Abstract

OBJECTIVE

Following our observation that histone deacetylase inhibitors (HDACIs) trichostatin A (TSA) and valproic acid (VPA) can suppress proliferation of endometrial stromal cells, we sought to determine whether TSA and VPA do so by inducing cell cycle arrest and p21 expression.

STUDY DESIGN

A recently established immortalized endometrial stromal cell line was treated with TSA, VPA, and/or all-trans retinoic acid (ATRA) and the consequent cell cycle progression was measured by flow cytometry and p21 protein expression by Western blot analysis.

RESULTS

Both TSA and VPA induced cell cycle arrest and p21 expression in a concentration-dependent manner. Treatment with ATRA alone also induced cell cycle arrest and moderate increase in p21 expression but joint treatment of ATRA and TSA/VPA did not further enhance cell cycle arrest as compared with TSA/VPA treatment alone.

CONCLUSIONS

HDACIs suppress proliferation of endometrial stromal cells through induction of cell cycle arrest and possibly also through apoptosis as well. RA also induces cell cycle arrest but it does not synergize with HDACIs in inducing cell cycle arrest. HDACIs may be promising compounds for treating endometriosis.

摘要

目的

在观察到组蛋白去乙酰化酶抑制剂(HDACIs)曲古抑菌素A(TSA)和丙戊酸(VPA)可抑制子宫内膜基质细胞增殖后,我们试图确定TSA和VPA是否通过诱导细胞周期停滞和p21表达来实现这一作用。

研究设计

用TSA、VPA和/或全反式维甲酸(ATRA)处理最近建立的永生化子宫内膜基质细胞系,通过流式细胞术检测随后的细胞周期进程,并用蛋白质印迹分析检测p21蛋白表达。

结果

TSA和VPA均以浓度依赖的方式诱导细胞周期停滞和p21表达。单独用ATRA处理也诱导细胞周期停滞并使p21表达适度增加,但与单独用TSA/VPA处理相比,ATRA与TSA/VPA联合处理并未进一步增强细胞周期停滞。

结论

HDACIs通过诱导细胞周期停滞以及可能还通过凋亡来抑制子宫内膜基质细胞增殖。维甲酸也诱导细胞周期停滞,但在诱导细胞周期停滞方面它与HDACIs没有协同作用。HDACIs可能是治疗子宫内膜异位症的有前景的化合物。

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