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首页> 外文期刊>Biochemical and Biophysical Research Communications >CircRNA circ_0026344 as a prognostic biomarker suppresses colorectal cancer progression via microRNA-21 and microRNA-31
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CircRNA circ_0026344 as a prognostic biomarker suppresses colorectal cancer progression via microRNA-21 and microRNA-31

机译:CircRNA Circ_0026344作为预后生物标志物通过MicroRNA-21和MicroRNA-31抑制结肠直肠癌进展

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摘要

Recently, circular RNA (circRNA) is identified as a novel class of noncoding RNA with important roles in human diseases, such as cancer. However, how circRNA participates in colorectal cancer (CRC) remains unclear. In this study, we aimed to illustrate the role of circ_0026344 in CRC progression. We showed that circ_0026344 expression was downregulated in CRC tissues compared to adjacent normal tissues. Moreover, the level of circ_0026344 was inversely correlated with CRC advance and lymphoid node metastasis. Additionally, circ_0026344 low expression predicted poor prognosis in CRC patients. We identified circ_0026344 as a miRNA sponge for microRNA-21 (miR-21) and microRNA-31 (miR-31) whose expression levels were elevated in CRC tissues. And the level of circ_0026344 was reversely correlated with both miR-21 and miR-31 levels in CRC tissues. Functionally, we found that ectopic expression of circ_0026344 decreased the growth and invasion of CRC cells while promoting apoptosisin?vitro. The xenograft experiment indicated that circ_0026344 overexpress led to CRC growth inhibitionin?vivo. Rescue assays further demonstrated that circ_0026344 exerted biological functions by sponging miR-21 and miR-31 in CRC. In conclusion, this study revealed that circ_0026344/miR-21/miR-31 regulatory signaling was implicated in CRC progression.
机译:最近,循环RNA(CircrNA)被鉴定为具有重要作用的新型非分量RNA,具有癌症等人类疾病。但是,CircrNA如何参与结直肠癌(CRC)仍然尚不清楚。在这项研究中,我们旨在说明CRC进展中的Circ_0026344的作用。我们表明,与相邻的正常组织相比,CRC组织中的表达在CRC组织中下调。此外,Circ_0026344的水平与CRC提前和淋巴结转移相反。此外,CIRC_0026344低表达预测CRC患者的预后差。我们将Circ_0026344鉴定为miRRNA-21(miR-21)和microRNA-31(miR-31)的miRNA海绵,其表达水平在CRC组织中升高。 CIC_0026344的水平与CRC组织中的miR-21和miR-31水平反向相关。在功能上,我们发现Circ_0026344的异位表达降低了CRC细胞的生长和侵袭,同时促进凋亡素?体外。异种移植物实验表明,昼夜循环抑制率为CRC生长抑制素α体内。救援测定进一步证明了CIRC_0026344通过CRC中的MIR-21和MIR-31施加生物学功能。总之,本研究表明,循环_0026344 / miR-21 / miR-31调节信号传导涉及CRC进展。

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