首页> 美国卫生研究院文献>Aging (Albany NY) >LncRNA HIF1A-AS2 promotes osteosarcoma progression by acting as a sponge of miR-129-5p
【2h】

LncRNA HIF1A-AS2 promotes osteosarcoma progression by acting as a sponge of miR-129-5p

机译:LncRNA HIF1A-AS2通过充当miR-129-5p的海绵来促进骨肉瘤进展

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Increasing studies have demonstrated that long noncoding RNAs (lncRNAs) play vital roles in tumor development and progression. However, the relationship between osteosarcoma and HIF1AAS2 remains unknown. The expression of HIF1AAS2 and miR-129-5p was detected in osteosarcoma cell lines and samples via qRT-PCR. Cell Counting Kit-8 (CCK-8) and invasion assays were performed to determine cell proliferation and invasion ability, and a dual luciferase reporter assay was performed to determine the interaction between HIF1AAS2 and miR-129-5p. We showed that the expression of HIF1A-AS2 was upregulated in the osteosarcoma samples compared with the expression in noncancerous samples. Moreover, patients with high HIF1A-AS2 expression had a shorter overall survival. Ectopic expression of HIF1A-AS2 enhanced osteosarcoma cell proliferation, cell cycle progression and invasion. We found that overexpression of miR-129-5p decreased the luciferase activity of wild-type (WT) HIF1A-AS2 but not mutant HIF1A-AS2. Ectopic expression of HIF1A-AS2 suppressed miR-129-5p expression in MG-63 cells. We demonstrated that miR-129-5p was downregulated in osteosarcoma and was negatively associated with HIF1A-AS2 expression. Furthermore, ectopic expression of miR-129-5p suppressed osteosarcoma cell proliferation, cell cycle progression and invasion. In addition, overexpression of HIF1A-AS2 promoted cell proliferation, cell cycle progression and invasion of osteosarcoma cells through the modulation of miR-129-5p. These results indicated that HIF1A-AS2 might be a potential therapeutic target for osteosarcoma.
机译:越来越多的研究表明,长的非编码RNA(lncRNA)在肿瘤的发生和发展中起着至关重要的作用。但是,骨肉瘤和HIF1AAS2之间的关系仍然未知。通过qRT-PCR在骨肉瘤细胞系和样品中检测到HIF1AAS2和miR-129-5p的表达。进行了Cell Counting Kit-8(CCK-8)和侵袭测定,以确定细胞增殖和侵袭能力,并进行了双重荧光素酶报告基因测定,以确定HIF1AAS2与miR-129-5p之间的相互作用。我们显示,与非癌性样品中的表达相比,HIF1A-AS2在骨肉瘤样品中的表达上调。此外,HIF1A-AS2高表达的患者的总生存期较短。 HIF1A-AS2的异位表达增强了骨肉瘤细胞增殖,细胞周期进程和侵袭。我们发现,miR-129-5p的过表达降低了野生型(WT)HIF1A-AS2的荧光素酶活性,但没有降低突变体HIF1A-AS2的荧光素酶活性。 HIF1A-AS2的异位表达抑制了MG-63细胞中miR-129-5p的表达。我们证明,miR-129-5p在骨肉瘤中被下调,并且与HIF1A-AS2表达负相关。此外,miR-129-5p的异位表达抑制骨肉瘤细胞增殖,细胞周期进程和侵袭。此外,HIF1A-AS2的过表达通过调节miR-129-5p促进了骨肉瘤细胞的增殖,细胞周期进程和侵袭。这些结果表明,HIF1A-AS2可能是骨肉瘤的潜在治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号