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lncRNA HOTTIP facilitates osteosarcoma cell migration invasion and epithelial-mesenchymal transition by forming a positive feedback loop with c-Myc

机译:lncRNA HOTTIP通过与c-Myc形成正反馈环来促进骨肉瘤细胞迁移侵袭和上皮间质转化

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摘要

Homeobox A transcript at the distal tip (HOTTIP) is an oncogenic long non-coding RNA in cancer. The aim of the present study was to investigate the function and mechanism of HOTTIP in the aggressive behaviors of human osteosarcoma (OS) cells. Expression levels of HOTTIP and epithelial-mesenchymal transition (EMT) markers were determined by reverse transcription-quantitative PCR. Cell invasive and migratory abilities were evaluated in vitro using Matrigel and wound healing assays, respectively. Knockdown of HOTTIP expression was achieved by small interfering RNA-mediated silencing. Overexpression of c-Myc was accomplished by transfecting cultured cells with a c-Myc overexpression plasmid. HOTTIP was demonstrated to be upregulated in OS tissues and cell lines; knockdown of HOTTIP inhibited OS cell migration, invasion and EMT, and suppressed c-Myc expression. In addition, overexpression of c-Myc increased HOTTIP expression and enhanced OS cell migration and invasion. HOTTIP promoted cell migration and invasion by upregulating c-Myc in OS. The positive feedback loop formed by HOTTIP and c-Myc may contribute to OS progression, and HOTTIP may act as a therapeutic target for OS.
机译:同源框远端的转录物(HOTTIP)是癌症中的致癌性长非编码RNA。本研究的目的是研究HOTTIP在人类骨肉瘤(OS)细胞侵袭行为中的功能和机制。通过逆转录定量PCR确定HOTTIP和上皮-间质转化(EMT)标记的表达水平。分别使用Matrigel和伤口愈合试验对细胞的侵袭和迁移能力进行了评估。抑制HOTTIP表达的方法是通过小的RNA干扰介导的沉默来实现的。通过用c-Myc过表达质粒转染培养的细胞来实现c-Myc的过表达。 HOTTIP被证明在OS组织和细胞系中表达上调;击倒HOTTIP抑制OS细胞迁移,侵袭和EMT,并抑制c-Myc表达。另外,c-Myc的过表达增加了HOTTIP表达并增强了OS细胞的迁移和侵袭。 HOTTIP通过上调OS中的c-Myc促进细胞迁移和侵袭。由HOTTIP和c-Myc形成的正反馈回路可能有助于OS进展,HOTTIP可以作为OS的治疗靶标。

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