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miR-107-5p 通过靶向雌激素受体-α促进子宫内膜癌的增殖和侵袭。

miR‑107‑5p promotes tumor proliferation and invasion by targeting estrogen receptor‑α in endometrial carcinoma.

机构信息

Department of Obstetrics and Gynecology, Shanghai General Hospital Affiliated with Shanghai Jiao Tong University School of Medicine, Shanghai 200080, P.R. China.

Department of Obstetrics and Gynecology, International Peace Maternity and Child Health Hospital Affiliated with Shanghai Jiao Tong University School of Medicine, Shanghai 200030, P.R. China.

出版信息

Oncol Rep. 2019 Mar;41(3):1575-1585. doi: 10.3892/or.2018.6936. Epub 2018 Dec 18.

Abstract

The aberrant expression of miR107‑5p is closely related to the development of several types of human cancers. However, the role of miR‑107‑5p in endometrial carcinoma (EC) has not been fully confirmed. In the present study, we aimed to explore the function of miR‑107‑5p in EC carcinogenesis. EC samples and normal endometrial tissues were obtained by laser capture microdissection. It was determined that the expression of miR‑107‑5p in EC was significantly higher than that in normal endometrium, and higher miR‑107‑5p expression was related to advanced FIGO stages, lymph node metastasis and myometrial invasion in EC patients. Blocking miR‑107‑5p significantly inhibited cell proliferation, migration and invasion of EC cells in vitro and in vivo. The results of bioinformatic algorithms and luciferase reporter assays revealed that estrogen receptor α (ERα) was a direct target of miR‑107‑5p. miR‑107‑5p downregulated the expression of ERα mRNA and protein. In conclusion, our results highlighted that miR‑107‑5p is a novel prognostic factor that targets ERα to promote tumor proliferation and invasion of EC.

摘要

miR107-5p 的异常表达与几种人类癌症的发展密切相关。然而,miR-107-5p 在子宫内膜癌(EC)中的作用尚未得到充分证实。在本研究中,我们旨在探讨 miR-107-5p 在 EC 发生中的作用。通过激光捕获显微切割获得 EC 样本和正常子宫内膜组织。结果表明,EC 中 miR-107-5p 的表达明显高于正常子宫内膜,并且 miR-107-5p 的高表达与 EC 患者的 FIGO 晚期分期、淋巴结转移和肌层浸润有关。阻断 miR-107-5p 显著抑制 EC 细胞在体外和体内的增殖、迁移和侵袭。生物信息学算法和荧光素酶报告基因检测结果表明,雌激素受体α(ERα)是 miR-107-5p 的直接靶标。miR-107-5p 下调 ERα mRNA 和蛋白的表达。综上所述,我们的研究结果表明,miR-107-5p 是一种新型的预后因子,通过靶向 ERα 促进 EC 的肿瘤增殖和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a9b/6365687/df57b1b092d5/OR-41-03-1575-g00.jpg

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