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四跨膜蛋白CD9受miR-518f-5p调控并在乳腺细胞迁移和体内肿瘤生长中发挥作用。

Tetraspanin CD9 is Regulated by miR-518f-5p and Functions in Breast Cell Migration and In Vivo Tumor Growth.

作者信息

Bond Danielle R, Kahl Richard, Brzozowski Joshua S, Jankowski Helen, Naudin Crystal, Pariyar Mamta, Avery-Kiejda Kelly A, Scarlett Christopher J, Boucheix Claude, Muller William J, Ashman Leonie K, Cairns Murray J, Roselli Séverine, Weidenhofer Judith

机构信息

School of Biomedical Science and Pharmacy, The University of Newcastle and Hunter Medical Research Institute (HMRI), Newcastle, NSW 2308, Australia.

Department of Pediatrics, Emory University, Atlanta, GA 30322, USA.

出版信息

Cancers (Basel). 2020 Mar 26;12(4):795. doi: 10.3390/cancers12040795.

Abstract

Breast cancer is the most commonly diagnosed and the second leading cause of cancer-related mortality among women worldwide. miR-518f-5p has been shown to modulate the expression of the metastasis suppressor CD9 in prostate cancer. However, the role of miR-518f-5p and CD9 in breast cancer is unknown. Therefore, this study aimed to elucidate the role of miR-518f-5p and the mechanisms responsible for decreased CD9 expression in breast cancer, as well as the role of CD9 in de novo tumor formation and metastasis. miR-518f-5p function was assessed using migration, adhesion, and proliferation assays. miR-518f-5p was overexpressed in breast cancer cell lines that displayed significantly lower CD9 expression as well as less endogenous CD9 3'UTR activity, as assessed using qPCR and dual luciferase assays. Transfection of miR-518f-5p significantly decreased CD9 protein expression and increased breast cell migration in vitro. Cd9 deletion in the MMTV/PyMT mouse model impaired tumor growth, but had no effect on tumor initiation or metastasis. Therefore, inhibition of miR-518f-5p may restore CD9 expression and aid in the treatment of breast cancer metastasis.

摘要

乳腺癌是全球女性中最常被诊断出的癌症,也是癌症相关死亡的第二大主要原因。在前列腺癌中,miR-518f-5p已被证明可调节转移抑制因子CD9的表达。然而,miR-518f-5p和CD9在乳腺癌中的作用尚不清楚。因此,本研究旨在阐明miR-518f-5p的作用以及乳腺癌中CD9表达降低的机制,以及CD9在肿瘤形成和转移中的作用。使用迁移、黏附和增殖试验评估miR-518f-5p的功能。通过qPCR和双荧光素酶试验评估,miR-518f-5p在显示出显著较低CD9表达以及较少内源性CD9 3'UTR活性的乳腺癌细胞系中过表达。miR-518f-5p转染显著降低了CD9蛋白表达,并增加了体外乳腺细胞迁移。在MMTV/PyMT小鼠模型中敲除Cd9会损害肿瘤生长,但对肿瘤起始或转移没有影响。因此,抑制miR-518f-5p可能会恢复CD9表达,并有助于治疗乳腺癌转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ef/7226392/d088b13d359f/cancers-12-00795-g001.jpg

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