LINC00858 facilitates the malignant development of Wilms' Tumor by targeting miR-653-5p.

IF 4.7 4区医学 0 MEDICINE, GENERAL & INTERNAL

Minerva medica Pub Date : 2024-06-01 Epub Date: 2020-06-12 DOI:10.23736/S0026-4806.20.06566-0

Dan Zhou, Jilan Wang, Suping Xu, Zengming Li, Dan Kou

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引用次数: 0

Abstract

Background: To uncover the clinical significance of LINC00858 in the development of Wilms' Tumor and the potential molecular mechanism.

Methods: LINC00858 levels in Wilms' Tumor species and cell lines were determined by quantitative real-time polymerase chain reaction (qRT-PCR). The clinical significance of LINC00858 in influencing pathological features and prognosis in patients with Wilms' Tumor was analyzed. Proliferative and migratory changes in Wilms' Tumor cells with LINC00858 knockdown were assessed. The downstream gene of LINC00858 was verified by luciferase assay, and its involvement in the development of Wilms' Tumor was further explored.

Results: LINC00858 was highly expressed in Wilms' Tumor tissues and cell lines. High level of LINC00858 was correlated to high rate of lymphatic metastasis and poor prognosis in patients with Wilms' Tumor. Knockdown of LINC00858 suppressed proliferative and migratory potentials in HFWT and 17-94 cells. MiR-653-5p was targeted by LINC00858. It was lowly expressed in Wilms' Tumor tissues and negatively regulated by LINC00858. Knockdown of miR-653-5p partially abolished the regulatory effects of LINC00858 on proliferative and migratory potentials in Wilms' Tumor cells.

Conclusions: LINC00858 is highly expressed in Wilms' Tumor species and correlated to lymphatic metastasis rate and overall survival in patients with Wilms' Tumor. Knockdown of LINC00858 suppresses Wilms' Tumor cells to proliferate and migrate via targeting miR-653-3p.

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LINC00858 通过靶向 miR-653-5p 促进了 Wilms 肿瘤的恶性发展。

背景：揭示LINC00858在Wilms's肿瘤发生中的临床意义及潜在的分子机制：揭示LINC00858在Wilms's肿瘤发生发展中的临床意义和潜在的分子机制：方法：通过实时定量聚合酶链式反应（qRT-PCR）测定Wilms'肿瘤物种和细胞系中的LINC00858水平。分析了 LINC00858 在影响 Wilms 肿瘤患者病理特征和预后方面的临床意义。评估了 LINC00858 基因敲除后 Wilms 肿瘤细胞的增殖和迁移变化。通过荧光素酶实验验证了LINC00858的下游基因，并进一步探讨了其在Wilms'肿瘤发生发展中的参与作用：结果：LINC00858在Wilms'肿瘤组织和细胞系中高表达。结果：LINC00858在Wilms'肿瘤组织和细胞系中高表达，其高水平与Wilms'肿瘤患者的高淋巴转移率和预后不良相关。敲除 LINC00858 可抑制 HFWT 和 17-94 细胞的增殖和迁移潜能。LINC00858靶向了MiR-653-5p。它在 Wilms 肿瘤组织中低表达，并受 LINC00858 的负调控。敲除 miR-653-5p 可部分消除 LINC00858 对 Wilms 肿瘤细胞增殖和迁移潜能的调控作用：LINC00858在Wilms'肿瘤中高表达，并与Wilms'肿瘤患者的淋巴转移率和总生存率相关。敲除 LINC00858 可通过靶向 miR-653-3p 抑制 Wilms 肿瘤细胞的增殖和迁移。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Minerva medica 医学-医学：内科

CiteScore

6.40

自引率

6.40%

发文量

358

审稿时长

>12 weeks

期刊介绍： Minerva Medica publishes scientific papers on internal medicine. Manuscripts may be submitted in the form of editorials, original articles, review articles, case reports, special articles, letters to the Editor and guidelines. The journal aims to provide its readers with papers of the highest quality and impact through a process of careful peer review and editorial work. Duties and responsibilities of all the subjects involved in the editorial process are summarized at Publication ethics.