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人类髓母细胞瘤中的微小RNA分析

MicroRNA profiling in human medulloblastoma.

作者信息

Ferretti Elisabetta, De Smaele Enrico, Po Agnese, Di Marcotullio Lucia, Tosi Emanuele, Espinola Maria Salome B, Di Rocco Concezio, Riccardi Riccardo, Giangaspero Felice, Farcomeni Alessio, Nofroni Italo, Laneve Pietro, Gioia Ubaldo, Caffarelli Elisa, Bozzoni Irene, Screpanti Isabella, Gulino Alberto

机构信息

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

出版信息

Int J Cancer. 2009 Feb 1;124(3):568-77. doi: 10.1002/ijc.23948.

Abstract

Medulloblastoma is an aggressive brain malignancy with high incidence in childhood. Current treatment approaches have limited efficacy and severe side effects. Therefore, new risk-adapted therapeutic strategies based on molecular classification are required. MicroRNA expression analysis has emerged as a powerful tool to identify candidate molecules playing an important role in a large number of malignancies. However, no data are yet available on human primary medulloblastomas. A high throughput microRNA expression profiles was performed in human primary medulloblastoma specimens to investigate microRNA involvement in medulloblastoma carcinogenesis. We identified specific microRNA expression patterns which distinguish medulloblastoma differing in histotypes (anaplastic, classic and desmoplastic), in molecular features (ErbB2 or c-Myc overexpressing tumors) and in disease-risk stratification. MicroRNAs expression profile clearly differentiates medulloblastoma from either adult or fetal normal cerebellar tissues. Only a few microRNAs displayed upregulated expression, while most of them were downregulated in tumor samples, suggesting a tumor growth-inhibitory function. This property has been addressed for miR-9 and miR-125a, whose rescued expression promoted medulloblastoma cell growth arrest and apoptosis while targeting the proproliferative truncated TrkC isoform. In conclusion, misregulated microRNA expression profiles characterize human medulloblastomas, and may provide potential targets for novel therapeutic strategies.

摘要

髓母细胞瘤是一种侵袭性脑恶性肿瘤,在儿童期发病率较高。目前的治疗方法疗效有限且副作用严重。因此,需要基于分子分类的新的风险适应性治疗策略。微小RNA表达分析已成为识别在大量恶性肿瘤中起重要作用的候选分子的有力工具。然而,关于人类原发性髓母细胞瘤尚无相关数据。我们对人类原发性髓母细胞瘤标本进行了高通量微小RNA表达谱分析,以研究微小RNA在髓母细胞瘤致癌过程中的作用。我们鉴定出了特定的微小RNA表达模式,这些模式可区分组织学类型(间变性、经典型和促纤维增生型)、分子特征(ErbB2或c-Myc过表达肿瘤)以及疾病风险分层不同的髓母细胞瘤。微小RNA表达谱能清楚地将髓母细胞瘤与成人或胎儿正常小脑组织区分开来。只有少数微小RNA显示表达上调,而大多数在肿瘤样本中表达下调,提示其具有肿瘤生长抑制功能。我们已对miR-9和miR-125a进行了研究,它们的表达恢复可促进髓母细胞瘤细胞生长停滞和凋亡,同时靶向促增殖的截短型TrkC异构体。总之,微小RNA表达谱失调是人类髓母细胞瘤的特征,可能为新的治疗策略提供潜在靶点。

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