Cancer Biology & Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Nat Genet. 2011 Jun 5;43(7):673-8. doi: 10.1038/ng.858.
The importance of individual microRNAs (miRNAs) has been established in specific cancers. However, a comprehensive analysis of the contribution of miRNAs to the pathogenesis of any specific cancer is lacking. Here we show that in T-cell acute lymphoblastic leukemia (T-ALL), a small set of miRNAs is responsible for the cooperative suppression of several tumor suppressor genes. Cross-comparison of miRNA expression profiles in human T-ALL with the results of an unbiased miRNA library screen allowed us to identify five miRNAs (miR-19b, miR-20a, miR-26a, miR-92 and miR-223) that are capable of promoting T-ALL development in a mouse model and which account for the majority of miRNA expression in human T-ALL. Moreover, these miRNAs produce overlapping and cooperative effects on tumor suppressor genes implicated in the pathogenesis of T-ALL, including IKAROS (also known as IKZF1), PTEN, BIM, PHF6, NF1 and FBXW7. Thus, a comprehensive and unbiased analysis of miRNA action in T-ALL reveals a striking pattern of miRNA-tumor suppressor gene interactions in this cancer.
个体 microRNAs(miRNAs)的重要性已在特定癌症中得到证实。然而,对于 miRNA 对任何特定癌症发病机制的贡献,还缺乏全面的分析。在这里,我们表明在 T 细胞急性淋巴细胞白血病(T-ALL)中,一小部分 miRNA 负责协同抑制多个肿瘤抑制基因。对人类 T-ALL 中的 miRNA 表达谱与无偏 miRNA 文库筛选的结果进行交叉比较,使我们能够鉴定出五种能够在小鼠模型中促进 T-ALL 发展的 miRNA(miR-19b、miR-20a、miR-26a、miR-92 和 miR-223),并且这些 miRNA 占人类 T-ALL 中 miRNA 表达的大部分。此外,这些 miRNA 对涉及 T-ALL 发病机制的肿瘤抑制基因(包括 IKAROS(也称为 IKZF1)、PTEN、BIM、PHF6、NF1 和 FBXW7)产生重叠和协同作用。因此,对 T-ALL 中 miRNA 作用的全面和无偏分析揭示了这种癌症中 miRNA-肿瘤抑制基因相互作用的惊人模式。