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微小 RNA-143 在骨肉瘤中下调,通过靶向 Bcl-2 促进细胞凋亡并抑制肿瘤生成。

microRNA-143, down-regulated in osteosarcoma, promotes apoptosis and suppresses tumorigenicity by targeting Bcl-2.

机构信息

Department of Orthopedics, Changhai Hospital, Second Military Medical University, Shanghai 200433, PR China.

出版信息

Oncol Rep. 2010 Nov;24(5):1363-9. doi: 10.3892/or_00000994.

Abstract

Deregulated microRNAs and their roles in tumorigenesis are still largely unknown. Here, we focused on the roles of miR-143 in osteosarcoma, as previous reports have suggested its importance in some other types of cancer. We found that miR-143 was down-regulated in osteosarcoma cell lines and primary tumor samples, and the restoration of miR-143 reduced cell viability, promoted cell apoptosis and suppressed tumorigenicity. Additionally, Bcl-2, an important antiapoptotic molecule, was identified to be a novel direct target of miR-143, and the proapoptotic function of miR-143 is further suggested to be mainly through the targeting of Bcl-2 expression. Collectively, our data identify the important roles of miR-143 in osteosarcoma pathogenesis and indicate its potential application in cancer therapy.

摘要

miR-143 在肿瘤发生中的作用及其调控机制尚不清楚。本研究旨在探讨 miR-143 在骨肉瘤中的作用,因为先前的研究表明其在其他一些类型的癌症中具有重要作用。研究发现 miR-143 在骨肉瘤细胞系和原发性肿瘤样本中表达下调,恢复 miR-143 的表达可降低细胞活力,促进细胞凋亡,抑制肿瘤生成。此外,Bcl-2 作为一种重要的抗凋亡分子,被鉴定为 miR-143 的一个新的直接靶标,miR-143 的促凋亡功能主要是通过靶向 Bcl-2 表达来实现的。综上所述,本研究结果表明 miR-143 在骨肉瘤发病机制中发挥着重要作用,并提示其在癌症治疗中的潜在应用价值。

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