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环状GLIS3/miR-644a/PTBP1正反馈环促进非小细胞肺癌的恶性生物学进展。

A circGLIS3/miR-644a/PTBP1 positive feedback loop promotes the malignant biological progressions of non-small cell lung cancer.

作者信息

Wu Zhixiong, Jiang Hong, Fu Hong, Zhang Yan

机构信息

Department of Oncology, Tongji Hospital of Tongji University Shanghai, China.

出版信息

Am J Cancer Res. 2021 Jan 1;11(1):108-122. eCollection 2021.

Abstract

Non-small cell lung cancer (NSCLC) is a severe cancer which critically threatens human health in the world. Circular RNAs (circRNAs) are non-coding RNAs that involve in cancer progression. We want to explore the roles of circRNAs in NSCLC in this study. In current study, circGLIS3 was found to be highly expressed in NSCLC tissues and cell lines and high circGLIS3 level was correlated to malignant characteristics and poor prognosis of NSCLC. Functional experiments suggested that circGLIS3 promoted proliferation, migration and invasion and arrested apoptosis of NSCLC cells in vitro. CircGLIS3 also participated in the in vivo process by accelerate NSCLC tumor growth and metastasis. Mechanistically, circGLIS3 could sponging multiple anti-cancer miRNAs including miR-526b, miR-198, miR-498 and miR-664a. Here, we for the first time confirmed that miR-644a was downregulated and functioned as a tumor suppression gene in NSCLC. In addition, we found PTBP1 as a novel target of miR-644a and circGLIS3 could raise the expression of PTBP1 via miR-644a. And PTBP1 could bind to the flanking introns of circGLIS3 and thereby promoting looping of circGLIS3. In conclusion, CircGLIS3 functions as an oncogene via sponging multiple tumor-suppressive miRNAs in NSCLC. A circGLIS3/miR-644a/PTBP1 positive feedback loop exists in the tumorigenesis and development of NSCLC.

摘要

非小细胞肺癌(NSCLC)是一种严重的癌症,在全球范围内严重威胁着人类健康。环状RNA(circRNAs)是非编码RNA,参与癌症进展。在本研究中,我们想探索circRNAs在NSCLC中的作用。在当前研究中,发现circGLIS3在NSCLC组织和细胞系中高表达,且circGLIS3水平高与NSCLC的恶性特征和不良预后相关。功能实验表明,circGLIS3在体外促进NSCLC细胞的增殖、迁移和侵袭,并阻止其凋亡。circGLIS3还通过加速NSCLC肿瘤生长和转移参与体内过程。机制上,circGLIS3可以 sponge 多种抗癌miRNA,包括miR-526b、miR-198、miR-498和miR-664a。在这里,我们首次证实miR-644a在NSCLC中下调并作为肿瘤抑制基因发挥作用。此外,我们发现PTBP1是miR-644a的新靶点,circGLIS3可以通过miR-644a提高PTBP1的表达。并且PTBP1可以结合circGLIS3的侧翼内含子,从而促进circGLIS3的环化。总之,circGLIS3在NSCLC中通过 sponge 多种肿瘤抑制性miRNA发挥癌基因作用。在NSCLC的发生发展中存在circGLIS3/miR-644a/PTBP1正反馈环。

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