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miR-223/Hsp70/JNK/JUN/miR-223反馈环调节骨肉瘤对顺铂的化疗耐药性。

miR-223/Hsp70/JNK/JUN/miR-223 feedback loop modulates the chemoresistance of osteosarcoma to cisplatin.

作者信息

Tang Qi, Yuan Qi, Li Hui, Wang Wanchun, Xie Guangrong, Zhu Kewei, Li Ding

机构信息

Department of Orthopedics, The Second Xiangya Hospital, Central South University, Changsha, Hunan, 410011, China.

Department of Hepatopathy, The Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, Hunan, 410002, China.

出版信息

Biochem Biophys Res Commun. 2018 Mar 11;497(3):827-834. doi: 10.1016/j.bbrc.2018.02.091. Epub 2018 Feb 9.

Abstract

Osteosarcoma (OS) is a primary bone malignancy with a five-year survival rate of 60%; the chemoresistance of OS still remains a huge challenge. Heat shock protein 70 (Hsp70), a member of HSP family, is overexpressed in OS cell lines and involved in the resistance of OS cell lines. In addition, miRNAs have been involved in the carcinogenesis and chemoresistance of OS; of them, miR-223 has been reported to be underexpressed and serve as a tumor suppressor in OS through targeting Hsp90B1, also a member of HSP family. Herein, online tools predicted that Hsp70 might be a direct target of miR-223. In the present study, miR-223 expression was down-regulated in OS tissues and cell lines; miR-223 overexpression enhanced the cellular effects of cisplatin (CDDP) on OS cell lines. Through binding to the HSPA1A 3'UTR, miR-223 could regulate Hsp70 protein levels and downstream JNK/JUN signaling pathway, thus modulating OS cell apoptosis through Hsp70 under CDDP stress. Finally, JUN, a downstream transcription factor of JNK signaling, could bind to the promoter region of miR-223 to promote its transcription. In summary, miR-223, Hsp70 and downstream JNK/JUN formed a feedback loop to modulate the chemoresistance of OS to CDDP.

摘要

骨肉瘤(OS)是一种原发性骨恶性肿瘤,其五年生存率为60%;OS的化疗耐药性仍然是一个巨大的挑战。热休克蛋白70(Hsp70)是热休克蛋白家族的成员之一,在OS细胞系中过表达,并参与OS细胞系的耐药性。此外,微小RNA(miRNA)已参与OS的致癌作用和化疗耐药性;其中,据报道miR-223表达下调,并通过靶向Hsp90B1(也是热休克蛋白家族的成员)在OS中发挥肿瘤抑制作用。在此,在线工具预测Hsp70可能是miR-223的直接靶点。在本研究中,miR-223在OS组织和细胞系中表达下调;miR-223过表达增强了顺铂(CDDP)对OS细胞系的细胞作用。通过与HSPA1A 3'非翻译区结合,miR-223可以调节Hsp70蛋白水平和下游JNK/JUN信号通路,从而在CDDP应激下通过Hsp70调节OS细胞凋亡。最后,JNK信号的下游转录因子JUN可以结合到miR-223的启动子区域以促进其转录。总之,miR-223、Hsp70和下游JNK/JUN形成了一个反馈环,以调节OS对CDDP的化疗耐药性。

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