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一种新型长链非编码RNA,即缺氧诱导因子-2α启动子上游转录本,在体外作为骨肉瘤干细胞的抑制剂发挥作用。

A novel long non-coding RNA, hypoxia-inducible factor-2α promoter upstream transcript, functions as an inhibitor of osteosarcoma stem cells in vitro.

作者信息

Wang Yongcheng, Yao Jie, Meng Haoye, Yu Zhiguo, Wang Zhigang, Yuan Xueling, Chen Hong, Wang Aiyuan

机构信息

Institute of Orthopedics, Chinese PLA General Hospital, Beijing 100853, P.R. China.

Department of Oncology, PLA No. 161 Center Hospital, Wuhan, Hubei 430000, P.R. China.

出版信息

Mol Med Rep. 2015 Apr;11(4):2534-40. doi: 10.3892/mmr.2014.3024. Epub 2014 Dec 1.

Abstract

Long non‑coding RNAs (lncRNAs) have recently been identified as novel modulators of malignant tumors. However, the function of lncRNAs in cancer stem cells (CSCs) remains to be elucidated. The present study aimed to investigate the regulating role of a novel lncRNA, hypoxia‑inducible factor‑2α (HIF‑2α) promoter upstream transcript (HIF2PUT), in osteosarcoma stem cells. The expression levels of HIF2PUT were assessed by quantitative polymerase chain reaction in 17 osteosarcoma tissue specimens, and the correlation between the expression of HIF2PUT and its host transcript‑HIF‑2α was determined. In functional experiments, HIF2PUT expression was knocked down by small interfering RNAs, or overexpressed by transfection with pcDNA‑HIF2PUT, in order to evaluate the effects of HIF2PUT on cell proliferation, migration, expression rate of osteosarcoma stem cell marker CD133, and stem sphere‑forming ability in MG63 cells. HIF2PUT expression levels were positively correlated with HIF‑2α in osteosarcoma tissues. Overexpression of HIF2PUT markedly inhibited cell proliferation and migration, decreased the percentage of CD133 expressing cells, and impaired the osteosarcoma stem sphere‑forming ability of the MG63 cells. Whereas, knockdown of HIF2PUT expression had the opposite effect. Furthermore, altering the expression of HIF2PUT resulted in a concomitant change to HIF‑2α mRNA expression. These results indicate that the lncRNA HIF2PUT may be a novel regulatory factor of osteosarcoma stem cells, which may exert its function partly by controlling HIF‑2α expression. Further studies regarding HIF2PUT may provide a novel therapeutic target of osteosarcoma in the future.

摘要

长链非编码RNA(lncRNAs)最近被确定为恶性肿瘤的新型调节因子。然而,lncRNAs在癌症干细胞(CSCs)中的功能仍有待阐明。本研究旨在探讨一种新型lncRNA,即缺氧诱导因子-2α(HIF-2α)启动子上游转录本(HIF2PUT)在骨肉瘤干细胞中的调节作用。通过定量聚合酶链反应评估17例骨肉瘤组织标本中HIF2PUT的表达水平,并确定HIF2PUT表达与其宿主转录本HIF-2α之间的相关性。在功能实验中,通过小干扰RNA敲低HIF2PUT表达,或用pcDNA-HIF2PUT转染使其过表达,以评估HIF2PUT对MG63细胞增殖、迁移、骨肉瘤干细胞标志物CD133表达率及干细胞球形成能力的影响。骨肉瘤组织中HIF2PUT表达水平与HIF-2α呈正相关。HIF2PUT过表达显著抑制细胞增殖和迁移,降低CD133表达细胞的百分比,并损害MG63细胞的骨肉瘤干细胞球形成能力。而敲低HIF2PUT表达则产生相反的效果。此外,改变HIF2PUT的表达导致HIF-2α mRNA表达随之改变。这些结果表明,lncRNA HIF2PUT可能是骨肉瘤干细胞的一种新型调节因子,其可能部分通过控制HIF-2α表达发挥作用。关于HIF2PUT的进一步研究可能为未来骨肉瘤提供新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/686f/4337490/9564ab01ac1b/MMR-11-04-2534-g01.jpg

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