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Long noncoding RNA LINC01510 promotes the growth of colorectal cancer cells by modulating MET expression

机译:长非编码RNA LINC01510通过调节MET表达促进结直肠癌细胞的生长

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Abnormal expression of long non-coding RNA (lncRNAs) often facilitates unrestricted growth of cancer cells. Long intergenic non-protein coding RNA 1510, an enhancer lncRNA (LINC01510), a lncRNA enhancer is upregulated in colorectal cancer (CRC), and its expression might relate to MET as revealed by lncRNA microarray data. However, the potential biological role of LINC01510 and its regulatory mechanism in CRC remain unclear. Therefore, we investigated the involvement of LINC01510 in the proliferation of CRC cells. Microarray analysis, In situ hybridization, colony formation assay, MTT assay, Western blotting, quantitative RT-PCR and flow cytometry were applied. The two-tailed Student’s t test and analysis of variance or general linear model of single factor variable was used for statistical analyse. In the present study, we found that LINC01510 was significantly upregulated in CRC tissues and cell lines. The LINC01510 expression level were associated with the clinicopathological grade and stage. Meanwhile, gain- and loss-of-function assays demonstrated that LINC01510 overexpression increased CRC cell proliferation, and promoted cell cycle progression from the G1 phase to the S phase. Further study indicated that LINC01510 was positively correlated with the expression of MET, and its effects were most likely at the transcriptional level. Taken together, our findings suggested that upregulation of LINC01510 contributes to the proliferation of CRC cells, at least in part, through the regulation of MET protein. LINC01510 could be a candidate prognostic biomarker and a target for new therapies in CRC patients.
机译:长的非编码RNA(lncRNA)的异常表达通常促进癌细胞的不受限制的生长。长基因间非蛋白编码RNA 1510,增强子lncRNA(LINC01510),lncRNA增强子在结直肠癌(CRC)中被上调,如lncRNA基因芯片数据所揭示,其表达可能与MET有关。但是,LINC01510的潜在生物学作用及其在CRC中的调控机制仍不清楚。因此,我们研究了LINC01510与CRC细胞增殖的关系。应用了微阵列分析,原位杂交,集落形成测定,MTT测定,Western印迹,定量RT-PCR和流式细胞仪。使用两尾学生t检验和方差分析或单因素变量的一般线性模型进行统计分析。在本研究中,我们发现LINC01510在CRC组织和细胞系中显着上调。 LINC01510表达水平与临床病理学分级和阶段有关。同时,功能获得和功能丧失分析表明LINC01510过表达增加了CRC细胞增殖,并促进了细胞周期从G1期到S期的发展。进一步的研究表明,LINC01510与MET的表达呈正相关,其作用最可能在转录水平上。综上所述,我们的发现表明,LINC01510的上调至少部分通过调节MET蛋白来促进CRC细胞的增殖。 LINC01510可能是候选的预后生物标志物,并且是CRC患者新疗法的靶标。

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