Wu Balu, Liu Guohong, Jin Yanxia, Yang Tian, Zhang Dongdong, Ding Lu, Zhou Fuling, Pan Yunbao, Wei Yongchang
Department of Hematology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Department of Radiology, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Front Oncol. 2020 Feb 26;10:108. doi: 10.3389/fonc.2020.00108. eCollection 2020.
MicroRNAs (miRNAs) can participate in many behaviors of various tumors. Prior studies have reported that miR-15b-5p in different tumors can either promote or inhibit tumor progression. In breast cancer, the role of miR-15b-5p is unclear. The main objective of this paper is to explore miR-15b-5p effects and their mechanisms in breast cancer using both and experiments. This study showed that miR-15b-5p expression was upregulated in breast cancer compared with normal breast tissue and was positively correlated with poor overall survival in patients. Knockdown of miR-15b-5p in MCF-7 and MD-MBA-231 breast cancer cells restrained cell growth and invasiveness and induced apoptosis, whereas overexpression of miR-15b-5p achieved the opposite effects. We next revealed a negative correlation between miR-15b-5p and heparanase-2 (HPSE2) expression in breast cancer. Knockdown of miR-15b-5p significantly increased HPSE2 expression at both mRNA and protein levels in breast cancer cells . The underlying mechanisms of miR-15-5p in breast cancer were investigated using luciferase activity reporter assay and rescue experiments. In addition, miR-15b-5p knockdown significantly inhibited tumor growth in a xenograft model in mice. In summary, we showed that miR-15b-5p promotes breast cancer cell proliferation, migration, and invasion by directly targeting HPSE2. Accordingly, miR-15b-5p may serve both as a tool for prognosis and as a target for therapy of breast cancer patients.
微小RNA(miRNA)可参与多种肿瘤的多种行为。先前的研究报道,不同肿瘤中的miR-15b-5p既可以促进也可以抑制肿瘤进展。在乳腺癌中,miR-15b-5p的作用尚不清楚。本文的主要目的是通过体内和体外实验探索miR-15b-5p在乳腺癌中的作用及其机制。本研究表明,与正常乳腺组织相比,miR-15b-5p在乳腺癌中的表达上调,且与患者较差的总生存期呈正相关。在MCF-7和MD-MBA-231乳腺癌细胞中敲低miR-15b-5p可抑制细胞生长和侵袭并诱导凋亡,而miR-15b-5p的过表达则产生相反的效果。接下来,我们发现乳腺癌中miR-15b-5p与乙酰肝素酶-2(HPSE2)的表达呈负相关。敲低miR-15b-5p可显著提高乳腺癌细胞中HPSE2在mRNA和蛋白质水平的表达。使用荧光素酶活性报告基因检测和挽救实验研究了miR-15-5p在乳腺癌中的潜在机制。此外,敲低miR-15b-5p可显著抑制小鼠异种移植模型中的肿瘤生长。总之,我们表明miR-15b-5p通过直接靶向HPSE2促进乳腺癌细胞的增殖、迁移和侵袭。因此,miR-15b-5p既可以作为乳腺癌患者预后的工具,也可以作为治疗靶点。