首页> 外文期刊>Cancer biotherapy and radiopharmaceuticals >YY1-Induced Upregulation of Long Noncoding RNA ARAP1-AS1 Promotes Cell Migration and Invasion in Colorectal Cancer Through the Wnt/beta-Catenin Signaling Pathway
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YY1-Induced Upregulation of Long Noncoding RNA ARAP1-AS1 Promotes Cell Migration and Invasion in Colorectal Cancer Through the Wnt/beta-Catenin Signaling Pathway

机译:YY1诱导的长度非编码RNA ARAP1-AS1的上调促进通过WNT /β-Catenin信号通路促进结肠直肠癌中的细胞迁移和侵袭

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Introduction: It has been reported that long noncoding RNAs (lncRNAs) are crucial regulators in progression of human cancers, including colorectal cancer (CRC). However, the function of lncRNA ARAP1 antisense RNA 1 (ARAP1-AS1) in CRC remains unclear. Aim: The aim of this study was to investigate the function and molecular mechanism of lncRNA ARAP1-AS1 in CRC. Results: ARAP1-AS1 was highly expressed in CRC tissues and cell lines. ARAP1-AS1 knockdown suppressed cell migration, invasion, and epithelial-mesenchymal transition (EMT). YY1 transcription factor (YY1) enhanced the transcription activity of ARAP1-AS1. The YY1/ARAP1-AS1 axis promoted CRC cell migration and invasion. YY1/ARAP1-AS1 could regulate the Wnt/beta-catenin signaling pathway. Conclusions: This study revealed that YY1-induced upregulation of ARAP1-AS1 promoted cell migration, invasion, and EMT process in CRC through the Wnt/beta-catenin signaling pathway.
机译:介绍:据报道,长期非编码RNA(LNCRNA)是人类癌症进展中的关键调节因子,包括结肠直肠癌(CRC)。 然而,CRC中LNCRNA ARAP1反义RNA 1(ARAP1-AS1)的功能仍不清楚。 目的:本研究的目的是研究CRC中LNCRNA ARAP1-AS1的功能和分子机制。 结果:ARAP1-AS1在CRC组织和细胞系中高度表达。 ARAP1-AS1敲除抑制细胞迁移,侵袭和上皮间充质转换(EMT)。 YY1转录因子(YY1)增强了ARAP1-AS1的转录活性。 YY1 / ARAP1-AS1轴促进了CRC细胞迁移和侵袭。 YY1 / ARAP1-AS1可以调节WNT / BETA-Catenin信号通路。 结论:本研究表明,YY1诱导的ARAP1-AS1促进细胞迁移,侵袭和CRC中的EMT过程通过WNT /β-catenin信号传导途径。

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