Shi Ji, Gong Lijie, Chen Legao, Luo Jungang, Song Guangyuan, Xu Ji, Lv Zhenye, Tao Houquan, Xia Yingjie, Ye Zaiyuan
Zhejiang Province Tongde Hospital, Hangzhou, Zhejiang, China.
Key Laboratory of Gastroenterology of Zhejiang Province, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, Zhejiang, China.
Anat Rec (Hoboken). 2019 Jun;302(6):931-940. doi: 10.1002/ar.24083. Epub 2019 Feb 25.
Recent studies have demonstrated that microRNAs regulate gene expression and are related to cancer progression. Increasing evidence shows that miR-618 plays an important role in a variety of tumors, including thyroid carcinomas, breast cancer and lymphoma cancer. However, no studies have examined the expression or function of miR-618 in gastric cancer (GC). In this study, we examined the effects and molecular mechanisms of miR-618 in GC. We compared the expression levels of miR-618 in 90 paired GC tissues and adjacent noncancerous tissues. Cell cycle, apoptosis and transwell assays were performed in GC cells with miR-618 mimic or inhibitor in vitro. We first used quantitative PCR(qPCR) to show that miR-618 expression levels were downregulated in GC tissues, which showed statistical significance. Next we used transwell assays to prove that miR-618 suppressed the invasion and migration capacity of GC cells. Furthermore, screening of the miRDB and Target Scan Human databases indicated TGF-β2 as a downstream target of miR-618. In further research, we identified TGF-β2 as a target gene of miR-618 by the luciferase reporter assay. Western blot analysis confirmed that TGF-β2 expression was inversely correlated with miR-618 expression. In situ hybridization showed that miR-618 expression level was downregulated in GC tissues. In conclusion, our findings suggest that miR-618 may function as a tumor suppressor in GC and suppresses metastasis in GC by negatively regulating the transcriptional level of TGF-β2. Anat Rec, 302:931-940, 2019. © 2019 Wiley Periodicals, Inc.
最近的研究表明,微小RNA可调节基因表达并与癌症进展相关。越来越多的证据表明,miR-618在包括甲状腺癌、乳腺癌和淋巴瘤在内的多种肿瘤中发挥重要作用。然而,尚无研究检测miR-618在胃癌(GC)中的表达或功能。在本研究中,我们检测了miR-61八在GC中的作用及其分子机制。我们比较了90对GC组织和癌旁非癌组织中miR-618的表达水平。在体外对转染了miR-618模拟物或抑制剂的GC细胞进行细胞周期、凋亡和Transwell实验。我们首先使用定量PCR(qPCR)显示GC组织中miR-618表达水平下调,具有统计学意义。接下来,我们使用Transwell实验证明miR-618抑制了GC细胞的侵袭和迁移能力。此外,通过对miRDB和Target Scan Human数据库的筛选,表明TGF-β2是miR-618的下游靶点。在进一步的研究中,我们通过荧光素酶报告基因实验确定TGF-β2是miR-618的靶基因。蛋白质免疫印迹分析证实TGF-β2的表达与miR-618的表达呈负相关。原位杂交显示GC组织中miR-618表达水平下调。总之,我们的研究结果表明,miR-618在GC中可能起肿瘤抑制作用,并通过负调控TGF-β2的转录水平抑制GC转移。《解剖学记录》,302:931 - 940,2019年。©2019威利期刊公司。