Suppr超能文献

EWSR1 过表达是多发性骨髓瘤中的一个致癌事件。

EWSR1 overexpression is a pro-oncogenic event in multiple myeloma.

机构信息

Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto, 602-8566, Japan.

Department of Hematology, Fukuchiyama City Hospital, Fukuchiyama, Japan.

出版信息

Int J Hematol. 2021 Mar;113(3):381-394. doi: 10.1007/s12185-020-03027-0. Epub 2020 Oct 23.

Abstract

Multiple myeloma (MM) is cytogenetically, genetically and molecularly heterogenous even among subclones in one patient, therefore, it is essential to identify both frequent and patient-specific drivers of molecular abnormality. Following previous molecular investigations, we in this study investigated the expression patterns and function of the Ewing sarcoma breakpoint region 1 (EWSR1) gene in MM. The EWSR1 transcriptional level in CD138-positive myeloma cells was higher in 36.4% of monoclonal gammopathy of undetermined significance, in 67.4% of MM patients compared with normal plasma cells, and significantly higher in ten human myeloma-derived cell lines (HMCLs) examined. EWSR1 gene knockdown caused growth inhibition with an increase of apoptotic cells in NCI-H929 and KMS-12-BM cells. Gene expression profiling using microarray analysis suggested EWSR1 gene knockdown caused transcriptional modulation of several genes associated with processes such as cell proliferation, cell motility, cell metabolism, and gene expression. Of particular, EWSR1 gene knockdown caused upregulation of let-7c and downregulation of its known targets K-RAS and AKT. Finally, our analysis using community database suggested that high EWSR1 expression positively associates with poor prognosis and advanced disease stage in MM. These findings suggest that EWSR1 overexpression is a pro-oncogenic molecular abnormality that may participate in MM progression.

摘要

多发性骨髓瘤(MM)即使在同一患者的亚克隆中也存在细胞遗传学、遗传学和分子异质性,因此,识别频繁出现的和患者特异性的分子异常驱动因素至关重要。在之前的分子研究之后,我们在这项研究中调查了尤文肉瘤断点区域 1(EWSR1)基因在 MM 中的表达模式和功能。在 36.4%的意义未明单克隆丙种球蛋白血症、67.4%的 MM 患者的 CD138 阳性骨髓瘤细胞中,EWSR1 的转录水平高于正常浆细胞,并且在 10 个人类骨髓瘤衍生细胞系(HMCL)中显著升高。EWSR1 基因敲低导致 NCI-H929 和 KMS-12-BM 细胞的生长抑制和凋亡细胞增加。使用微阵列分析的基因表达谱分析表明,EWSR1 基因敲低导致与细胞增殖、细胞迁移、细胞代谢和基因表达等过程相关的几个基因的转录调节。特别地,EWSR1 基因敲低导致 let-7c 的上调和其已知靶标 K-RAS 和 AKT 的下调。最后,我们使用社区数据库的分析表明,高 EWSR1 表达与 MM 中的不良预后和晚期疾病阶段呈正相关。这些发现表明 EWSR1 过表达是一种致癌的分子异常,可能参与 MM 的进展。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验