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LINC00641通过靶向miR-320a抑制卵巢癌细胞的增殖和侵袭。

LINC00641 inhibits the proliferation and invasion of ovarian cancer cells by targeting miR-320a.

作者信息

Li Yan, Lv Mengmeng, Wang Jianhua, Gao Chengzhen, Wu Yuzhong

机构信息

Department of Obstetrics and Gynecology, The Yancheng Clinical College of Xuzhou Medical University & The First People's Hospital of Yancheng, Yancheng, China.

Department of Gynecologic Oncology, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research & The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Transl Cancer Res. 2021 Nov;10(11):4894-4904. doi: 10.21037/tcr-21-2314.

Abstract

BACKGROUND

Ovarian cancer is a common malignancy of the female reproductive system, with one of the highest mortality rates among all malignant tumors. However, the pathogenesis of ovarian cancer has not been fully elucidated. This study investigated the role and molecular mechanism of LINC00641 in the development and progression of ovarian cancer.

METHODS

Quantitative real-time polymerase chain reaction (qRT-PCR) was used to detect the expression level of LINC00641 in ovarian cancer tissue and adjacent normal tissue. Cell Counting Kit-8 (CCK-8), colony formation, and Transwell assays were used to detect the effects of LINC00641 overexpression on the proliferation and migration of ovarian cancer cells. Bioinformatics analysis and luciferase reporter gene assay were employed to detect the binding of LINC00641 to the downstream target molecule, microRNA-320a (miR-320a). Western blotting was used to determine the effect of miR-320a overexpression on the expression of proliferation-related proteins [Ki-67 and proliferating cell nuclear antigen (PCNA)] and invasion-related proteins (E-cadherin, N-cadherin, and vimentin) in overexpressed LINC00641 cells.

RESULTS

qRT-PCR results showed that LINC00641 was under-expressed in ovarian cancer tissue compared to adjacent tissue. Cell function experiments showed that the overexpression of LINC00641 could significantly inhibit the proliferation and migration of ovarian cancer cells. The luciferase reporter gene assay showed that LINC00641 could bind to miR-320a, and the overexpression of LINC00641 could markedly inhibit the expression of miR-320a in ovarian cancer cells. Overexpression of miR-320a could significantly block the inhibitory effect of LINC00641 on the proliferation and migration of ovarian cancer cells.

CONCLUSIONS

As a tumor suppressor gene, LINC00641 can inhibit the proliferation and invasion of ovarian cancer cells by targeting miR-320a. The LINC00641/miR-320a axis may be a new target for the early diagnosis, treatment, or prognosis of ovarian cancer patients.

摘要

背景

卵巢癌是女性生殖系统常见的恶性肿瘤,在所有恶性肿瘤中死亡率位居前列。然而,卵巢癌的发病机制尚未完全阐明。本研究旨在探讨LINC00641在卵巢癌发生发展中的作用及分子机制。

方法

采用定量实时聚合酶链反应(qRT-PCR)检测LINC00641在卵巢癌组织及癌旁正常组织中的表达水平。运用细胞计数试剂盒-8(CCK-8)、集落形成实验和Transwell实验检测LINC00641过表达对卵巢癌细胞增殖和迁移的影响。通过生物信息学分析和荧光素酶报告基因实验检测LINC00641与下游靶分子微小RNA-320a(miR-320a)的结合情况。采用蛋白质免疫印迹法检测miR-320a过表达对LINC00641过表达细胞中增殖相关蛋白[Ki-67和增殖细胞核抗原(PCNA)]及侵袭相关蛋白(E-钙黏蛋白、N-钙黏蛋白和波形蛋白)表达的影响。

结果

qRT-PCR结果显示,与癌旁组织相比,LINC00641在卵巢癌组织中表达下调。细胞功能实验表明,LINC00641过表达可显著抑制卵巢癌细胞的增殖和迁移。荧光素酶报告基因实验显示,LINC00641可与miR-320a结合,LINC00641过表达可显著抑制卵巢癌细胞中miR-320a的表达。miR-320a过表达可显著阻断LINC00641对卵巢癌细胞增殖和迁移的抑制作用。

结论

作为一种肿瘤抑制基因,LINC00641可通过靶向miR-320a抑制卵巢癌细胞的增殖和侵袭。LINC00641/miR-320a轴可能成为卵巢癌患者早期诊断、治疗或预后评估的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0720/8798150/33795b3d557a/tcr-10-11-4894-f1.jpg

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