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全反式维甲酸调节子宫肌瘤中 PI3K 和维甲酸信号蛋白的变化。

All-trans-retinoic acid mediates changes in PI3K and retinoic acid signaling proteins of leiomyomas.

机构信息

Department of Obstetrics and Gynecology, Hadassah-Hebrew University Medical Center, Ein-Kerem, Jerusalem, Israel.

出版信息

Fertil Steril. 2011 May;95(6):2080-6. doi: 10.1016/j.fertnstert.2011.01.155. Epub 2011 Feb 26.

DOI:10.1016/j.fertnstert.2011.01.155
PMID:21354561
Abstract

OBJECTIVE

To detect changes induced by all-trans-retinoic acid (ATRA) on the expression and activation of target proteins of the retinoic acid (RA) and PI3K/Akt pathways involved in leiomyoma growth.

DESIGN

A study on human tissue cultures.

SETTING

Hadassah University Hospital.

PATIENT(S): Premenopausal women with uterine leiomyomas.

INTERVENTION(S): Paired cultures of normal myometrium and leiomyomas, from women undergoing hysterectomy, were obtained.

MAIN OUTCOME MEASURE(S): The effect of ATRA was examined on the expression and phosphorylation of relevant RA, PI3K/Akt, and Bcl2 proteins (immunochemical analysis), cell proliferation, cell cycle distribution, and apoptosis.

RESULT(S): Applying our cell culture model, we demonstrated that ATRA induced changes in the expression and activation of the RA and PI3K/Akt pathway proteins in leiomyoma cells, with significant increases of alcohol dehydrogenase 1 and cyclin D2 protein levels. In part of the leiomyoma cells, ATRA induced a relative increase of Bax (proapoptotic) as well as a relative decrease of phosphorylated glycogen synthase kinase 3β (proapoptotic).

CONCLUSION(S): Our results highlight the involvement of ATRA in the RA and PI3K/Akt pathways, whose specific signaling products may influence the outcome of leiomyoma growth by regulating cell proliferation, apoptosis, and survival. These results might be useful for the on-going research into alternative methods for treating and preventing this disorder.

摘要

目的

检测全反式维甲酸(ATRA)对涉及子宫肌瘤生长的维甲酸(RA)和 PI3K/Akt 通路靶蛋白表达和激活的变化。

设计

人体组织培养研究。

地点

哈达萨大学医院。

患者

行子宫切除术的绝经前子宫肌瘤妇女。

干预措施

从接受子宫切除术的妇女中获得正常子宫肌层和子宫肌瘤的配对培养物。

主要观察指标

检测 ATRA 对相关 RA、PI3K/Akt 和 Bcl2 蛋白(免疫化学分析)表达和磷酸化、细胞增殖、细胞周期分布和细胞凋亡的影响。

结果

应用我们的细胞培养模型,我们证明 ATRA 诱导子宫肌瘤细胞中 RA 和 PI3K/Akt 通路蛋白的表达和激活发生变化,醇脱氢酶 1 和细胞周期蛋白 D2 蛋白水平显著增加。在部分子宫肌瘤细胞中,ATRA 诱导 Bax(促凋亡)的相对增加和磷酸化糖原合成激酶 3β(促凋亡)的相对减少。

结论

我们的结果强调了 ATRA 参与 RA 和 PI3K/Akt 通路,其特定的信号产物可能通过调节细胞增殖、凋亡和存活来影响子宫肌瘤生长的结果。这些结果可能对正在进行的治疗和预防这种疾病的替代方法的研究有用。

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