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LINC01614 通过 miR-520a-3p/SNX3 轴促进骨肉瘤进展。

LINC01614 promotes osteosarcoma progression via miR-520a-3p/SNX3 axis.

机构信息

The Key Laboratory of Zoonosis Research, Chinese Ministry of Education, College of Basic Medical Science, Jilin University, Changchun 130021, China.

Orthopaedic Medical Center, The Second Hospital of Jilin University, Changchun 130041, China.

出版信息

Cell Signal. 2021 Jul;83:109985. doi: 10.1016/j.cellsig.2021.109985. Epub 2021 Mar 20.

Abstract

Long noncoding RNAs (lncRNAs) have been reported as essential regulators in osteosarcoma (OS), the most malignant bone tumor usually observed in children and adolescents. In the present study, we detected differentially expressed lncRNAs among OS tissues through RNA-sequencing. Then through bioinformatics analysis, we constructed the aberrant lncRNAs regulatory networks, and detected the key-lncRNAs. We identified LINC01614 was most significantly up-regulated among OS tissues, which was positively correlated with the worse prognosis. Through related in vitro experiments, we confirmed that knockdown of LINC01614 could inhibit the proliferation, invasion, and metastasis activities of OS cells. Furthermore, we identified LINC01614 may promote the proliferation and invasion activities of OS cells, via binding miR-520a-3p and increase the expression of SNX3. In conclusion, we identified lncRNAs participate in various malignant behaviors in OS. We also proved that LINC01614 could function as competing endogenous RNAs and promote the proliferation, and invasion of OS cells through miR-520a-3p/SNX3 axis, and thus acts as a novel prognostic marker for OS in clinic.

摘要

长链非编码 RNA(lncRNAs)已被报道为骨肉瘤(OS)中必不可少的调节因子,OS 是儿童和青少年中最常见的恶性骨肿瘤。在本研究中,我们通过 RNA 测序检测了 OS 组织中差异表达的 lncRNAs。然后通过生物信息学分析,构建了异常 lncRNAs 调控网络,并检测了关键-lncRNAs。我们发现 LINC01614 在 OS 组织中表达最显著上调,与预后较差呈正相关。通过相关的体外实验,我们证实敲低 LINC01614 可抑制 OS 细胞的增殖、侵袭和转移活性。此外,我们发现 LINC01614 可能通过结合 miR-520a-3p 并增加 SNX3 的表达,促进 OS 细胞的增殖和侵袭活性。总之,我们发现 lncRNAs 参与了 OS 中的各种恶性行为。我们还证明,LINC01614 可以作为竞争性内源性 RNA,通过 miR-520a-3p/SNX3 轴促进 OS 细胞的增殖和侵袭,因此可作为 OS 临床的一种新的预后标志物。

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