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肿瘤进展新途径的鉴定:HMGA1蛋白上调MicroRNA-181b并下调CBX7

Identification of a New Pathway for Tumor Progression: MicroRNA-181b Up-Regulation and CBX7 Down-Regulation by HMGA1 Protein.

作者信息

Mansueto Gelsomina, Forzati Floriana, Ferraro Angelo, Pallante Pierlorenzo, Bianco Mimma, Esposito Francesco, Iaccarino Antonino, Troncone Giancarlo, Fusco Alfredo

机构信息

Dipartimento di Biologia e Patologia Cellulare e Molecolare, Istituto di Endocrinologia ed Oncologia Sperimentale del CNR, Università di Napoli "Federico II", Naples, Italy.

出版信息

Genes Cancer. 2010 Mar;1(3):210-24. doi: 10.1177/1947601910366860.

Abstract

High mobility group A (HMGA) overexpression plays a critical role in neoplastic transformation. To investigate whether HMGA acts by regulating the expression of microRNAs, we analyzed the microRNA expression profile of human breast adenocarcinoma cells (MCF7) transfected with the HMGA1 gene, which results in a highly malignant phenotype. Among the microRNAs induced by HMGA1, we focused on miR-181b, which was overexpressed in several malignant neoplasias including breast carcinomas. We show that miR-181b regulates CBX7 protein levels, which are down-regulated in cancer, and promotes cell cycle progression. We also demonstrate that CBX7, being negatively regulated by HMGA, is able to negatively regulate miR-181b expression. Finally, there was a direct correlation between HMGA1 and miR-181b expression and an inverse correlation between HMGA1 and CBX7 expression in human breast carcinomas. These data indicate the presence of a novel pathway involving HMGA1, miR-181b, and CBX7, which leads to breast cancer progression.

摘要

高迁移率族蛋白A(HMGA)的过表达在肿瘤转化中起关键作用。为了研究HMGA是否通过调节微小RNA的表达发挥作用,我们分析了转染HMGA1基因的人乳腺腺癌细胞(MCF7)的微小RNA表达谱,该基因会导致高度恶性表型。在HMGA1诱导的微小RNA中,我们重点关注了miR-181b,它在包括乳腺癌在内的几种恶性肿瘤中均有过表达。我们发现miR-181b调节CBX7蛋白水平,CBX7在癌症中表达下调,且miR-181b促进细胞周期进程。我们还证明,受HMGA负调控的CBX7能够负向调节miR-181b的表达。最后,在人乳腺癌中,HMGA1与miR-181b的表达呈正相关,而HMGA1与CBX7的表达呈负相关。这些数据表明存在一条涉及HMGA1、miR-181b和CBX7的新途径,该途径导致乳腺癌进展。

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