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长链非编码RNA LINC00689通过海绵化miR-526b-3p上调ADAM9促进胃癌进展。

LncRNA LINC00689 Promotes the Progression of Gastric Cancer Through Upregulation of ADAM9 by Sponging miR-526b-3p.

作者信息

Yin Gang, Tian PeiRong, BuHe Amin, Yan Wei, Li TianXiong, Sun ZhiPeng

机构信息

Oncology Surgery Department, Beijing Shijitan Hospital, Capital Medical University (Peking University Ninth School of Clinical Medicine), Beijing 100038, People's Republic of China.

出版信息

Cancer Manag Res. 2020 Jun 4;12:4227-4239. doi: 10.2147/CMAR.S231042. eCollection 2020.

DOI:10.2147/CMAR.S231042
PMID:32581594
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7280092/
Abstract

INTRODUCTION

Increasing studies have demonstrated that noncoding RNAs, including miRNAs and lncRNAs, have vital roles in mediating cancer progression. However, the expression features and biological functions of LINC00689 in gastric cancer (GC) remain largely unknown. This study was designed to investigate the functions of LINC00689, miR-526b-3p and ADAM9 as well as their interactions in GC.

METHODS

Real time PCR(RT-PCR) was used to detect the expression of LINC0068, miR-526b-3p and ADAM9 in both GC tissues or cell lines. Gain- and loss- of functions of assays were conducted to verify the role of LINC0068, miR-526b-3p and ADAM9 in GC development. Cell proliferation were determined by CCK8 assay and transwell assay and scratch wound-healing assay were used to test cell invasion and migration. Further, the relationships between LINC00689 and miR-526b-3p, miR-526b-3p and ADAM9 were predicted by bioinformatics analysis and then proved by Luciferase reporter assay and RNA Immunoprecipitation(RIP) assay.

RESULTS

We found that LINC00689 was upregulated in GC tissues and positively correlated with advanced tumor stage and tumor size, while miR-526b-3p was downregulated. Furthermore, gain- and loss-of-function experiments revealed that LINC00689 promoted the proliferation, migration, invasion and epithelial-mesenchymal transition (EMT) of GC cells, while miR-526b-3p had the opposite effects. The underlying mechanisms indicated that LINC00689 functioned as a competing endogenous RNA (ceRNA) by sponging miR-526b-3p in GC cells. Further investigations confirmed that ADAM9 was a direct target of miR-526b-3p and positively modulated the progression of GC.

CONCLUSION

Our study suggests that LINC00689 functions as a novel oncogenic lncRNA in the development of GC by promoting ADAM9 expression through suppression of miR-526b-3p.

摘要

引言

越来越多的研究表明,包括微小RNA(miRNA)和长链非编码RNA(lncRNA)在内的非编码RNA在介导癌症进展中起着至关重要的作用。然而,LINC00689在胃癌(GC)中的表达特征和生物学功能仍 largely未知。本研究旨在探讨LINC00689、miR-526b-3p和ADAM9的功能及其在GC中的相互作用。

方法

采用实时定量聚合酶链反应(RT-PCR)检测LINC0068、miR-526b-3p和ADAM9在GC组织或细胞系中的表达。进行功能获得和功能缺失实验以验证LINC0068、miR-526b-3p和ADAM9在GC发生发展中的作用。通过CCK8法检测细胞增殖,采用Transwell实验和划痕伤口愈合实验检测细胞侵袭和迁移。此外,通过生物信息学分析预测LINC00689与miR-526b-3p、miR-526b-3p与ADAM9之间的关系,然后通过荧光素酶报告基因实验和RNA免疫沉淀(RIP)实验进行验证。

结果

我们发现LINC00689在GC组织中上调,且与肿瘤晚期和肿瘤大小呈正相关,而miR-526b-3p下调。此外,功能获得和功能缺失实验表明,LINC00689促进GC细胞的增殖、迁移、侵袭和上皮-间质转化(EMT),而miR-526b-3p则具有相反的作用。潜在机制表明,LINC00689在GC细胞中通过海绵吸附miR-526b-3p发挥竞争性内源RNA(ceRNA)的作用。进一步研究证实,ADAM9是miR-526b-3p的直接靶点,并正向调节GC的进展。

结论

我们的研究表明,LINC00689在GC发生发展中作为一种新型致癌lncRNA,通过抑制miR-526b-3p促进ADAM9表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/cf7ca029af89/CMAR-12-4227-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/e27ca291a8e7/CMAR-12-4227-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/2afc563e9d9d/CMAR-12-4227-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/055915b61edd/CMAR-12-4227-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/cf7ca029af89/CMAR-12-4227-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/e27ca291a8e7/CMAR-12-4227-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/57e518730d0a/CMAR-12-4227-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/f4ede3ba06ae/CMAR-12-4227-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/68dd4de85ffc/CMAR-12-4227-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/2afc563e9d9d/CMAR-12-4227-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/055915b61edd/CMAR-12-4227-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07d4/7280092/cf7ca029af89/CMAR-12-4227-g0007.jpg

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