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沉默含菱形结构域蛋白1以抑制人乳腺癌细胞的转移

Silencing of rhomboid domain containing 1 to inhibit the metastasis of human breast cancer cells .

作者信息

Huang Chunjun, Ji Xiaochun, Peng Yinyin, Wu Minghua, Wu Weizhu, Luo Yong, Cheng Gaoxiang, Zhu Ye

机构信息

Thyroid Breast Surgery, Ningbo Medical Center Lihuili Eastern Hospital, Ningbo, 315000, China.

Thyroid Breast Surgery, Ningbo Medical Center Lihuili Hospital, Ningbo, 315000, China.

出版信息

Iran J Basic Med Sci. 2018 Nov;21(11):1161-1166. doi: 10.22038/IJBMS.2018.29788.7191.

DOI:10.22038/IJBMS.2018.29788.7191
PMID:30483390
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6251397/
Abstract

OBJECTIVES

A growing body of evidence indicates that rhomboid domain containing 1 (RHBDD1) plays an important role in a variety of physiological and pathological processes, including tumorigenesis. We aimed to determine the function of RHBDD1 in breast cancer cells.

MATERIALS AND METHODS

In this study, we used the Oncomine™ database to determine the expression patterns of RHBDD1 in normal and breast cancer tissues. We performed lentiviral transfection of RHBDD1-specific small interfering RNA into the breast cancer cell lines ZR-75-30 and MDA-MB-231 in order to investigate the effects of RHBDD1 deficiency on breast cancer metastasis.

RESULTS

We found that knockdown of inhibited breast cancer cell migration and invasion . Moreover, knockdown of promoted epithelial-mesenchymal transition (EMT) by suppressing the expression of MPP2, MPP9, fibronectin 1, vimentin, SRY-box 2, zinc finger E-box binding homeobox 1, and snail family transcriptional repressor 1, and promoting the expression of cadherin 1. Additionally, knockdown of inhibited the protein expression and phosphorylation of Akt.

CONCLUSION

Our data indicate that RHBDD1 overexpression may promote breast cancer metastasis via the regulation of EMT, suggesting that RHBDD1 may be an important regulator of breast cancer metastasis.

摘要

目的

越来越多的证据表明,含菱形结构域蛋白1(RHBDD1)在包括肿瘤发生在内的多种生理和病理过程中发挥重要作用。我们旨在确定RHBDD1在乳腺癌细胞中的功能。

材料与方法

在本研究中,我们使用Oncomine™数据库来确定RHBDD1在正常和乳腺癌组织中的表达模式。我们将针对RHBDD1的特异性小干扰RNA进行慢病毒转染至乳腺癌细胞系ZR-75-30和MDA-MB-231中,以研究RHBDD1缺失对乳腺癌转移的影响。

结果

我们发现敲低[此处原文缺失具体基因名]可抑制乳腺癌细胞的迁移和侵袭。此外,敲低[此处原文缺失具体基因名]通过抑制MPP2、MPP9、纤连蛋白1、波形蛋白、SRY盒转录因子2、锌指E盒结合同源盒蛋白1和蜗牛家族转录抑制因子1的表达,并促进钙黏蛋白1的表达,从而促进上皮-间质转化(EMT)。此外,敲低[此处原文缺失具体基因名]可抑制Akt的蛋白表达和磷酸化。

结论

我们的数据表明,RHBDD1的过表达可能通过调节EMT来促进乳腺癌转移,提示RHBDD1可能是乳腺癌转移的重要调节因子。

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