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GABPB1-AS1 通过靶向 miRNA-566/F-box 蛋白 47 发挥肿瘤抑制因子的作用,抑制非小细胞肺癌的进展。

GABPB1-AS1 acts as a tumor suppressor and inhibits non-small cell lung cancer progression by targeting miRNA-566/F-box protein 47.

机构信息

Department of Pulmonary and Critical Care Medicine, Maoming People's Hospital, Maoming, China.

Department of Clinical Laboratory, Maoming People's Hospital, Maoming, China.

出版信息

Oncol Res. 2022 Nov 10;29(6):401-409. doi: 10.32604/or.2022.025262. eCollection 2021.

Abstract

It has been certified that GABPB1-AS1 is aberrantly expressed and plays as a vital role in some kinds of cancers. However, its expression pattern and functions in non-small cell lung cancer (NSCLC) are still largely unknown. This study aims to assess GABPB1-AS1 expression and biological roles in NSCLC. The expression of GABPB1-AS1 was detected in NSCLC specimens and adjacent normal specimens. CCK8 and Transwell assays were performed to evaluate the effects of GABPB1-AS1 on NSCLC cell proliferation, migration and invasion. Bioinformatics tools and luciferase reporter assays were applied to predict and verify GABPB1-AS1's direct targets. The results revealed that GABPB1-AS1 is sharply reduced in NSCLC specimens and cell lines. CCK8 assays indicated that overexpression of GABPB1-AS1 dramatically reduced NSCLC cell growth, and Transwell assays proved that NSCLC cell migration and invasion were distinctly inhibited by GABPB1-AS1. Exploration of the mechanism uncovered that miRNA-566 (miR-566)/F-box protein 47 (FBXO47) is directly targeted by GABPB1-AS1 in NSCLC. The study demonstrated that GABPB1-AS1 inhibited NSCLC cell proliferation, migration and invasion by targeting miR-566/FBXO47.

摘要

已证实 GABPB1-AS1 表达异常,并在某些癌症中发挥重要作用。然而,其在非小细胞肺癌(NSCLC)中的表达模式和功能仍知之甚少。本研究旨在评估 GABPB1-AS1 在 NSCLC 中的表达和生物学作用。检测了 NSCLC 标本和相邻正常标本中 GABPB1-AS1 的表达。CCK8 和 Transwell 测定法用于评估 GABPB1-AS1 对 NSCLC 细胞增殖、迁移和侵袭的影响。生物信息学工具和荧光素酶报告基因测定法用于预测和验证 GABPB1-AS1 的直接靶标。结果表明,GABPB1-AS1 在 NSCLC 标本和细胞系中明显减少。CCK8 测定法表明,GABPB1-AS1 的过表达显著降低了 NSCLC 细胞的生长,Transwell 测定法证明 GABPB1-AS1 明显抑制了 NSCLC 细胞的迁移和侵袭。机制探索表明,miRNA-566(miR-566)/F 盒蛋白 47(FBXO47)是 GABPB1-AS1 在 NSCLC 中的直接靶标。该研究表明,GABPB1-AS1 通过靶向 miR-566/FBXO47 抑制 NSCLC 细胞的增殖、迁移和侵袭。

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