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微小RNA-21通过PTEN/Akt信号通路促进人骨肉瘤细胞系MG63的增殖、侵袭并抑制其凋亡。

MicroRNA-21 promotes proliferation, invasion and suppresses apoptosis in human osteosarcoma line MG63 through PTEN/Akt pathway.

作者信息

Lv Chen, Hao Yuehan, Tu Guanjun

机构信息

Department of Orthopedics, The First Affiliated Hospital of China Medical University, No. 155 Nanjingbei Street, Heping District, Shenyang, 110001, China.

Department of Neurology, The First Affiliated Hospital of China Medical University, Shenyang, 110001, Liaoning, China.

出版信息

Tumour Biol. 2016 Jul;37(7):9333-42. doi: 10.1007/s13277-016-4807-6. Epub 2016 Jan 16.

Abstract

Osteosarcoma, which accounts for 5 % of pediatric tumor, remains the major cause of death among orthopedic malignancies. However, the factors associated with its malignant biological behavior are still poorly understood. MicroRNAs are a class of small noncoding RNAs, which have been considered to associate with malignant progression including cell differentiation, proliferation, apoptosis, invasion, and distant metastasis. In our research, we found that microRNA-21 (miR-21) was significantly overexpressed in human osteosarcoma cell line MG63 compared to human fetal osteoblastic cell line hFOB1.19 by using quantitative real-time polymerase chain reaction (qRT-PCR). Moreover, miR-21 overexpression in MG63 caused a significant raise in cell proliferation and invasion and a significant reduction in cell apoptosis. However, miR-21 underexpression in MG63 caused an opposite result. Western blotting displayed that proteins related with proliferation, apoptosis, and invasion were significantly changed in different groups, respectively. Furthermore, we demonstrated that PTEN may be a potential target of miR-21 in MG63 cells and miR-21 could activate PI3K/Akt pathway by suppressing PTEN expression. In summary, our findings suggested that miR-21 played an active role in osteosarcoma and it could predict the occurrence and development of osteosarcoma.

摘要

骨肉瘤占儿童肿瘤的5%,仍是骨科恶性肿瘤死亡的主要原因。然而,与其恶性生物学行为相关的因素仍知之甚少。微小RNA是一类小的非编码RNA,已被认为与包括细胞分化、增殖、凋亡、侵袭和远处转移在内的恶性进展有关。在我们的研究中,通过定量实时聚合酶链反应(qRT-PCR)发现,与人类胎儿成骨细胞系hFOB1.19相比,微小RNA-21(miR-21)在人类骨肉瘤细胞系MG63中显著过表达。此外,MG63中miR-21的过表达导致细胞增殖和侵袭显著增加,细胞凋亡显著减少。然而,MG63中miR-21的低表达则产生相反的结果。蛋白质印迹显示,不同组中与增殖、凋亡和侵袭相关的蛋白质分别发生了显著变化。此外,我们证明PTEN可能是MG63细胞中miR-21的潜在靶点,miR-21可通过抑制PTEN表达激活PI3K/Akt通路。总之,我们的研究结果表明,miR-21在骨肉瘤中发挥着积极作用,并且可以预测骨肉瘤的发生和发展。

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