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长链非编码 RNA XIST 通过海绵吸附 microRNA-448 来调控 GRHL2 促进结直肠癌细胞的恶性行为。

LncRNA XIST sponges microRNA-448 to promote malignant behaviors of colorectal cancer cells via regulating GRHL2.

机构信息

General Surgery Department, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, No. 99 LongCheng Street, Taiyuan, 030001, Shanxi, China.

Department of Breast Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, No. 99 LongCheng Street, Taiyuan, 030001, Shanxi, China.

出版信息

Funct Integr Genomics. 2022 Oct;22(5):977-988. doi: 10.1007/s10142-022-00873-5. Epub 2022 Jun 20.

Abstract

Long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) are essential regulators in human cancers, while the role of lncRNA X-inactive-specific transcript (XIST) in colorectal cancer (CRC) via regulating miR-448 remains largely unknown. Herein, we aimed to elucidate the effect of the XIST/miR-448/grainyhead-like 2 (GRHL2) axis on CRC development. XIST, miR-448, and GRHL2 expression in CRC tissues from patients and in human CRC cell lines was assessed. Loss- and gain-function assays were implemented to unveil the roles of XIST, miR-448, and GRHL2 in screened CRC cells. The tumor growth in vivo was observed in nude mice. Binding relations among XIST, miR-448, and GRHL2 were evaluated. XIST and GRHL2 expressed highly whereas miR-448 expressed lowly in CRC tissues and cells. XIST or GRHL2 downregulation, or miR-448 elevation suppressed the malignant behaviors of CRC cells in vitro, and downregulated XIST or upregulated miR-448 also inhibited the tumor growth in vivo. miR-448 upregulation reversed the role of XIST elevation in CRC cells. XIST particularly bound to miR-448, and miR-448 targeted GRHL2. Knockdown of XIST upregulates miR-448 to impede malignant behaviors of CRC cells via inhibiting GRHL2. This study may provide novel biomarkers for CRC diagnosis and treatment.

摘要

长链非编码 RNA(lncRNA)和 microRNA(miRNA)是人类癌症中的重要调节因子,而 X 染色体失活特异性转录物(XIST)通过调节 miR-448 在结直肠癌(CRC)中的作用在很大程度上尚不清楚。本文旨在阐明 XIST/miR-448/颗粒头样蛋白 2(GRHL2)轴对 CRC 发展的影响。评估了 XIST、miR-448 和 GRHL2 在患者 CRC 组织和人 CRC 细胞系中的表达。实施了缺失和增益功能测定,以揭示 XIST、miR-448 和 GRHL2 在筛选出的 CRC 细胞中的作用。在裸鼠中观察体内肿瘤生长。评估 XIST、miR-448 和 GRHL2 之间的结合关系。XIST 和 GRHL2 在 CRC 组织和细胞中高表达,而 miR-448 低表达。XIST 或 GRHL2 下调或 miR-448 上调体外抑制 CRC 细胞的恶性行为,下调 XIST 或上调 miR-448 也抑制体内肿瘤生长。miR-448 上调逆转了 XIST 升高在 CRC 细胞中的作用。XIST 特别与 miR-448 结合,miR-448 靶向 GRHL2。敲低 XIST 可上调 miR-448 通过抑制 GRHL2 来阻碍 CRC 细胞的恶性行为。这项研究可为 CRC 的诊断和治疗提供新的生物标志物。

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