Wei Min, Yu Hailang, Cai Cuixia, Gao Rui, Liu Xuhua, Zhu Huimin
Clinical Laboratory, Nanshan Maternity and Child Healthcare Hospital, Shenzhen, China.
Department of Science and Education, Nanshan Maternity and Child Healthcare Hospital, Shenzhen, China.
Front Oncol. 2020 Aug 7;10:1513. doi: 10.3389/fonc.2020.01513. eCollection 2020.
Increasing evidence indicates that the Aquaporin1 (AQP1) aberrant expression may be related to a wide variety of human cancers, including breast cancer (BC). In the present study, we explore the effects and possible mechanism of miR-3194-3p on the biological behaviors of BC. At first, miR-3194-3p is found to modulate expression targeting the 3'-UTR using miRNA target prediction algorithms. MiR-3194-3p expression is markedly downregulated, and expression is upregulated in BC tissues compared with adjacent normal breast tissues. Moreover, the differential expression of miR-3194-3p and are observed in four BC cells with different malignancy degree. Meanwhile, a significant negative correlation between and miR-3194-3p expressions in tumor tissues from 30 BC patients is revealed. miR-3194-3p mimic remarkably inhibits cell proliferation, migration, and invasion as well as promotes apoptosis in MDA-MB-231 cells while miR-3194-3p inhibitors exert an opposite role in MCF-7 cells. Dual-luciferase reporter system demonstrates that is a direct target gene of miR-3194-3p. Overexpression of by pBABE-puro- vector partially abrogates the effect of miR-3194-3p mimic in MDA-MB-231 cells. In short, our results suggest that miR-3194-3p suppresses BC cell proliferation, migration, and invasion by targeting , providing a novel insight into BC tumorigenesis and treatment.
越来越多的证据表明,水通道蛋白1(AQP1)异常表达可能与包括乳腺癌(BC)在内的多种人类癌症有关。在本研究中,我们探讨了miR - 3194 - 3p对BC生物学行为的影响及可能机制。首先,使用miRNA靶标预测算法发现miR - 3194 - 3p通过靶向3'-UTR调节表达。与相邻正常乳腺组织相比,miR - 3194 - 3p表达在BC组织中明显下调,而[此处原文缺失一个基因名称]表达上调。此外,在四种恶性程度不同的BC细胞中观察到miR - 3194 - 3p和 [此处原文缺失一个基因名称] 的差异表达。同时,揭示了30例BC患者肿瘤组织中[此处原文缺失一个基因名称]与miR - 3194 - 3p表达之间存在显著负相关。miR - 3194 - 3p模拟物显著抑制MDA - MB - 231细胞的增殖、迁移和侵袭,并促进其凋亡,而miR - 3194 - 3p抑制剂在MCF - 7细胞中发挥相反作用。双荧光素酶报告系统表明[此处原文缺失一个基因名称]是miR - 3194 - 3p的直接靶基因。通过pBABE - puro - 载体过表达[此处原文缺失一个基因名称]部分消除了miR - 3194 - 3p模拟物对MDA - MB - 231细胞的作用。简而言之,我们的结果表明miR - 3194 - 3p通过靶向[此处原文缺失一个基因名称]抑制BC细胞增殖、迁移和侵袭,为BC肿瘤发生和治疗提供了新的见解。