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GNAS-AS1/miR-4319/NECAB3 轴通过改变巨噬细胞极化促进非小细胞肺癌细胞的迁移和侵袭。

GNAS-AS1/miR-4319/NECAB3 axis promotes migration and invasion of non-small cell lung cancer cells by altering macrophage polarization.

机构信息

Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Tongji University, No. 507 Zhengming Road, Shanghai, 200433, China.

Department of Thoracic surgery, PLA General Hospital, No. 28 Fuxing Road, Beijing, 100853, China.

出版信息

Funct Integr Genomics. 2020 Jan;20(1):17-28. doi: 10.1007/s10142-019-00696-x. Epub 2019 Jul 3.

Abstract

Non-small cell lung cancer (NSCLC) represents for approximately 85% of all lung cancers, which is the most common cancer worldwide. Tumor-associated macrophages (TAM) are crucial for tumor progression, which was widely believed to be mediated by long non-coding RNAs (LncRNAs). We aimed to explore the effect of one LncRNA, GNAS-AS1, in TAM-associated NSCLC progression. Relative mRNA levels were determined by qRT-PCR. Western blot and ELISA were used to detect protein levels. Proliferation in vitro was assessed by MTT and clone formation assays. Migration and invasion of cell lines were evaluated by transwell-based assays. Interaction between molecules was detected by luciferase report assay. GNAS-AS1 expression was dramatically enhanced in TAM, NSCLC cell lines, and clinical tumor tissues, and negatively correlated with overall survival of NSCLC patients. GNAS-AS1 promoted macrophage M2 polarization and NSCLC cell progression via directly inhibiting miR-4319, which could target N-terminal EF-hand calcium binding protein 3 (NECAB3) to inhibit its expression. GNAS-AS1/miR-4319/NECAB3 axis promotes tumor progression of NSCLC by altering macrophage polarization. This novel mechanism may provide potential strategy for NSCLC treatment.

摘要

非小细胞肺癌(NSCLC)约占所有肺癌的 85%,是全球最常见的癌症。肿瘤相关巨噬细胞(TAM)对于肿瘤的进展至关重要,这被广泛认为是由长链非编码 RNA(LncRNA)介导的。我们旨在探索一种 LncRNA,即 GNAS-AS1,在与 TAM 相关的 NSCLC 进展中的作用。通过 qRT-PCR 确定相对 mRNA 水平。Western blot 和 ELISA 用于检测蛋白水平。体外增殖通过 MTT 和克隆形成测定评估。通过基于 Transwell 的测定评估细胞系的迁移和侵袭。通过荧光素酶报告测定检测分子之间的相互作用。GNAS-AS1 在 TAM、NSCLC 细胞系和临床肿瘤组织中表达明显增强,并与 NSCLC 患者的总生存率呈负相关。GNAS-AS1 通过直接抑制 miR-4319 促进巨噬细胞 M2 极化和 NSCLC 细胞进展,miR-4319 可以靶向 N 端 EF 手钙结合蛋白 3(NECAB3)抑制其表达。GNAS-AS1/miR-4319/NECAB3 轴通过改变巨噬细胞极化促进 NSCLC 肿瘤进展。这种新的机制可能为 NSCLC 的治疗提供潜在的策略。

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