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环状 RNA circEGFR 通过 miR-106a-5p/DDX5 轴调控结直肠癌的肿瘤进展。

Circular RNA circEGFR regulates tumor progression via the miR-106a-5p/DDX5 axis in colorectal cancer.

机构信息

Department of General Surgery, Jiangxi Provincial People's Hospital Affiliated to Nanchang University, Nanchang, Jiangxi, China.

Department of General Surgery, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.

出版信息

Braz J Med Biol Res. 2021 Jul 23;54(8):e10940. doi: 10.1590/1414-431X2020e10940. eCollection 2021.

Abstract

Recently, an increasing number of studies have reported that dysregulation of circular RNA (circRNA) expression plays critical roles in the progression of several cancers, including colorectal cancer (CRC). However, the detailed molecular mechanisms of circRNAs involvement in CRC remain largely unknown. Here, we confirmed that the level of circEGFR was significantly increased in CRC tissues compared to matched adjacent non-tumor tissues, and a high level of circEGFR was correlated with poor clinicopathological characteristics and poor prognosis in patients with CRC. Moreover, increased circEGFR expression promoted CRC cell proliferation, migration, and invasion in vitro. Mechanistically, circEGFR acted as a ceRNA for miR-106a-5p to relieve the repressive effect of miR-106a-5p on DDX5 mRNA. Moreover, circEGFR enhanced DDX5 expression, thereby upregulating p-AKT levels. Together, these findings showed that circEGFR promoted CRC cell proliferation, migration, and invasion through the miR-106a-5p/DDX5/AKT axis, and may serve as a promising diagnostic marker and therapeutic target for CRC patients.

摘要

最近,越来越多的研究报告称,环状 RNA(circRNA)表达失调在包括结直肠癌(CRC)在内的几种癌症的进展中发挥着关键作用。然而,circRNAs 参与 CRC 的详细分子机制在很大程度上仍然未知。在这里,我们证实 circEGFR 的水平在 CRC 组织中明显高于匹配的相邻非肿瘤组织,高水平的 circEGFR 与 CRC 患者的不良临床病理特征和预后不良相关。此外,circEGFR 的增加促进了 CRC 细胞在体外的增殖、迁移和侵袭。在机制上,circEGFR 作为 miR-106a-5p 的 ceRNA,减轻了 miR-106a-5p 对 DDX5 mRNA 的抑制作用。此外,circEGFR 增强了 DDX5 的表达,从而上调了 p-AKT 水平。综上所述,这些发现表明 circEGFR 通过 miR-106a-5p/DDX5/AKT 轴促进 CRC 细胞的增殖、迁移和侵袭,可能作为 CRC 患者有前途的诊断标志物和治疗靶点。

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