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人类实体瘤中复发性调控可变剪接事件的鉴定

Identification of recurrent regulated alternative splicing events across human solid tumors.

作者信息

Danan-Gotthold Miri, Golan-Gerstl Regina, Eisenberg Eli, Meir Keren, Karni Rotem, Levanon Erez Y

机构信息

Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan 52900, Israel.

Department of Biochemistry and Molecular Biology, the Institute for Medical Research Israel-Canada, Hebrew University-Hadassah Medical School, Ein Karem, 91120 Jerusalem, Israel.

出版信息

Nucleic Acids Res. 2015 May 26;43(10):5130-44. doi: 10.1093/nar/gkv210. Epub 2015 Apr 23.

Abstract

Cancer is a complex disease that involves aberrant gene expression regulation. Discriminating the modified expression patterns driving tumor biology from the many that have no or little contribution is important for understanding cancer molecular basis. Recurrent deregulation patterns observed in multiple cancer types are enriched for such driver events. Here, we studied splicing alterations in hundreds of matched tumor and normal RNA-seq samples of eight solid cancer types. We found hundreds of cassette exons for which splicing was altered in multiple cancer types and identified a set of highly frequent altered splicing events. Specific splicing regulators, including RBFOX2, MBNL1/2 and QKI, appear to account for many splicing alteration events in multiple cancer types. Together, our results provide a first global analysis of regulated splicing alterations in cancer and identify common events with a potential causative role in solid tumor development.

摘要

癌症是一种涉及异常基因表达调控的复杂疾病。从众多对肿瘤生物学没有贡献或贡献极小的表达模式中区分出驱动肿瘤生物学的修饰表达模式,对于理解癌症分子基础至关重要。在多种癌症类型中观察到的反复失调模式富含此类驱动事件。在此,我们研究了八种实体癌类型的数百对匹配肿瘤和正常RNA测序样本中的剪接改变。我们发现了数百个在多种癌症类型中剪接发生改变的盒式外显子,并鉴定出一组高度频繁的剪接改变事件。包括RBFOX2、MBNL1/2和QKI在内的特定剪接调节因子似乎在多种癌症类型中导致了许多剪接改变事件。总之,我们的结果首次对癌症中受调控的剪接改变进行了全局分析,并确定了在实体瘤发展中具有潜在致病作用的常见事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63c5/4446417/27ed5699ed27/gkv210fig1.jpg

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