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miR-129 通过抑制 TET1 参与子宫肌瘤的发生。

MiR-129 is involved in the occurrence of uterine fibroid through inhibiting TET1.

机构信息

Department of Gynecology and Obstetrics, The Second Hospital of Dalian Medical University, Dalian, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Jul;22(14):4419-4426. doi: 10.26355/eurrev_201807_15492.

Abstract

OBJECTIVE

To detect the expressions of micro ribonucleic acid (miR)-129 and its target gene in uterine fibroid tissues and to investigate the role of miR-129 in the occurrence of uterine fibroid.

PATIENTS AND METHODS

The expressions of miR-129 and its target gene ten-eleven translocation 1 (TET1) were detected via quantitative reverse transcription-polymerase chain reaction (qRT-PCR). Dual-luciferase reporter gene and Western blotting were used to verify the regulatory relation between miR-129 and target gene. The effects of miR-129 on the proliferation, apoptosis, cycle and extracellular matrix (ECM) of uterine fibroid cells were investigated via transfection with miR-129 mimics and TET1 small-interfering RNA (siRNA).

RESULTS

MiR-129 was lowly expressed in uterine fibroid. The expression of miR-129 was regulated by sex hormones. The highly expressed miR-129 promoted apoptosis and inhibited proliferation through reducing the low expression of TET1. At the same time, miR-129 affected the accumulation of ECM.

CONCLUSIONS

The expression of miR-129 in uterine fibroid is lower, and the proliferation capacity of tumor cells is enhanced, thus promoting the occurrence and development of uterine fibroid.

摘要

目的

检测微小核糖核酸(miR)-129 及其靶基因在子宫肌瘤组织中的表达,探讨 miR-129 在子宫肌瘤发生中的作用。

患者与方法

采用实时定量逆转录聚合酶链反应(qRT-PCR)检测 miR-129 及其靶基因 ten-eleven translocation 1(TET1)的表达。采用双荧光素酶报告基因和 Western blot 验证 miR-129 与靶基因的调控关系。通过转染 miR-129 模拟物和 TET1 小干扰 RNA(siRNA)研究 miR-129 对子宫肌瘤细胞增殖、凋亡、周期和细胞外基质(ECM)的影响。

结果

miR-129 在子宫肌瘤中低表达。miR-129 的表达受性激素调节。高表达的 miR-129 通过降低 TET1 的低表达促进凋亡并抑制增殖。同时,miR-129 影响 ECM 的积累。

结论

子宫肌瘤中 miR-129 的表达较低,肿瘤细胞的增殖能力增强,从而促进子宫肌瘤的发生发展。

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