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长链非编码 RNA-SNHG1 可能通过作为 miR-497 的海绵体促进非小细胞肺癌的进展。

Lnc-SNHG1 may promote the progression of non-small cell lung cancer by acting as a sponge of miR-497.

机构信息

Department of Intensive Care Unit, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.

Department of Respiratory Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China.

出版信息

Biochem Biophys Res Commun. 2018 Nov 30;506(3):632-640. doi: 10.1016/j.bbrc.2018.10.086. Epub 2018 Oct 25.

Abstract

Lnc-SNHG1 (small nucleolar RNA host gene 1) is considered an important regulating factor in several types of cancers. However, the biological functions and underlying molecular mechanisms in which lnc-SNHG1 is involved in non-small cell lung cancer (NSCLC) still need to be explored. In this study, we investigated the detailed effects and possible molecular mechanisms. The transcript level of lnc-SNHG1 was higher in lung adenocarcinoma specimens and NSCLC cell lines than in noncancer tissue and cells. The level of expression was positively correlated with invasiveness and was negatively correlated with the level of miR-497 in vivo and in vitro. In exploring the regulatory mechanism, we found that lnc-SNHG1 might modulate tumor growth by sponging miR-497. The inhibitory effect of si-lnc-SNHG1 on NSCLC cell proliferation, migration and invasion could be rescued by miR-497 inhibition, while the overexpression of miR-497 could reverse the effect of lnc-SNHG1 overexpression. Furthermore, our study demonstrated that the lnc-SNHG1 regulated the expression of the insulin-like growth factor 1 receptor (IGF1-R) by acting as a sponge of miR-497 in NSCLC. lnc-SNHG1 could be a novel biomarker as well as a curative target.

摘要

Lnc-SNHG1(小核仁 RNA 宿主基因 1)被认为是几种类型癌症中的重要调节因子。然而,lnc-SNHG1 在非小细胞肺癌(NSCLC)中所涉及的生物学功能和潜在的分子机制仍需要进一步探索。在本研究中,我们对其进行了详细的研究。lnc-SNHG1 在肺腺癌标本和 NSCLC 细胞系中的转录水平高于非癌组织和细胞。表达水平与侵袭性呈正相关,与体内和体外 miR-497 的水平呈负相关。在探索调控机制时,我们发现 lnc-SNHG1 可能通过海绵吸附 miR-497 来调节肿瘤生长。si-lnc-SNHG1 对 NSCLC 细胞增殖、迁移和侵袭的抑制作用可被 miR-497 抑制所挽救,而过表达 miR-497 则可逆转 lnc-SNHG1 过表达的作用。此外,我们的研究还表明,lnc-SNHG1 通过作为 miR-497 的海绵吸附物来调节 NSCLC 中胰岛素样生长因子 1 受体(IGF1-R)的表达。lnc-SNHG1 可能是一种新的生物标志物和治疗靶点。

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