Suppr超能文献

miR-374b 通过调控 FOXM1 减少宫颈癌的细胞增殖和侵袭。

MiR-374b reduces cell proliferation and cell invasion of cervical cancer through regulating FOXM1.

机构信息

Department of Gynaecology, Maternal and Child Health Hospital of HuBei Province, Wuhan, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Jan;23(2):513-521. doi: 10.26355/eurrev_201901_16863.

Abstract

OBJECTIVE

Deregulation of microRNAs (miRNAs) has been identified as critical event in tumor initiation and progression. We aimed to explore the role of miR-374b in cervical cancer progression.

PATIENTS AND METHODS

MiR-374b expression was detected using qRT-PCR in cervical cancer tissues compared with normal counterparts. Cell proliferation and invasion ability were detected using Cell Counting Kit-8 (CCK8) cell proliferation and transwell invasion assay. Dual luciferase reporter assay, qRT-PCR, and Western blot analysis were used to demonstrate that FOXM1 was a target of miR-374b.

RESULTS

We demonstrated that downregulation of miR-374b was frequently examined in cervical cancer tissues compared with normal counterparts. Furthermore, we showed the lower miR-374b expression associated with lymph node metastasis and advanced FIGO stage in patients with cervical cancer. Furthermore, ectopic expression of miR-374b could significantly decrease cell proliferation and invasion ability. However, inhibition of miR-374b had opposite effects. Dual luciferase reporter assay, qRT-PCR, and Western blot analysis revealed that miR-374b overexpression suppressed cell proliferation and invasion ability via affecting FOXM1 expression.

CONCLUSIONS

These results indicated that miR-374b acted as tumor suppressor and may serve as a potential target for cervical cancer treatment.

摘要

目的

microRNAs(miRNAs)的失调已被确定为肿瘤发生和进展的关键事件。我们旨在探讨 miR-374b 在宫颈癌进展中的作用。

患者和方法

采用 qRT-PCR 检测宫颈癌组织与正常对照中 miR-374b 的表达。采用细胞计数试剂盒-8(CCK8)细胞增殖和 Transwell 侵袭实验检测细胞增殖和侵袭能力。双荧光素酶报告基因实验、qRT-PCR 和 Western blot 分析用于证明 FOXM1 是 miR-374b 的靶基因。

结果

我们证明与正常对照相比,miR-374b 在宫颈癌组织中经常下调。此外,我们发现 miR-374b 表达水平较低与宫颈癌患者的淋巴结转移和 FIGO 晚期分期相关。此外,外源性表达 miR-374b 可显著降低细胞增殖和侵袭能力。然而,抑制 miR-374b 则有相反的效果。双荧光素酶报告基因实验、qRT-PCR 和 Western blot 分析表明,miR-374b 通过影响 FOXM1 表达来抑制细胞增殖和侵袭能力。

结论

这些结果表明,miR-374b 作为肿瘤抑制因子发挥作用,可能成为宫颈癌治疗的潜在靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验