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通过小 RNA 测序对人类 T 细胞急性淋巴细胞白血病进行全面的 miRNA 表达谱分析。

Comprehensive miRNA expression profiling in human T-cell acute lymphoblastic leukemia by small RNA-sequencing.

机构信息

Center for Medical Genetics Ghent, Ghent University, Ghent, Belgium.

Cancer Research Institute Ghent, Ghent, Belgium.

出版信息

Sci Rep. 2017 Aug 11;7(1):7901. doi: 10.1038/s41598-017-08148-x.

Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is a genetically heterogeneous disease that can be classified into different molecular genetic subtypes according to their mRNA gene expression profile. In this study, we applied RNA sequencing to investigate the full spectrum of miRNA expression in primary T-ALL patient samples, T-ALL leukemia cell lines and healthy donor thymocytes. Notably, this analysis revealed that genetic subtypes of human T-ALL also display unique miRNA expression signatures, which are largely conserved in human T-ALL cell lines with corresponding genetic background. Furthermore, small RNA-sequencing also unraveled the variety of isoforms that are expressed for each miRNA in T-ALL and showed that a significant number of miRNAs are actually represented by an alternative isomiR. Finally, comparison of CD34 and CD4CD8 healthy donor thymocytes and T-ALL miRNA profiles allowed identifying several novel miRNAs with putative oncogenic or tumor suppressor functions in T-ALL. Altogether, this study provides a comprehensive overview of miRNA expression in normal and malignant T-cells and sets the stage for functional evaluation of novel miRNAs in T-ALL disease biology.

摘要

T 细胞急性淋巴细胞白血病(T-ALL)是一种遗传异质性疾病,可以根据其 mRNA 基因表达谱分为不同的分子遗传亚型。在这项研究中,我们应用 RNA 测序来研究原发性 T-ALL 患者样本、T-ALL 白血病细胞系和健康供体胸腺细胞中完整的 miRNA 表达谱。值得注意的是,这项分析表明,人类 T-ALL 的遗传亚型也显示出独特的 miRNA 表达特征,这些特征在具有相应遗传背景的人类 T-ALL 细胞系中基本保守。此外,小 RNA 测序还揭示了每个 miRNA 在 T-ALL 中表达的各种异构体,并且表明大量 miRNA 实际上由替代的 isomiR 代表。最后,比较 CD34 和 CD4CD8 健康供体胸腺细胞和 T-ALL 的 miRNA 谱,鉴定出了一些在 T-ALL 中具有潜在致癌或肿瘤抑制功能的新 miRNA。总之,这项研究提供了正常和恶性 T 细胞中 miRNA 表达的全面概述,并为 T-ALL 疾病生物学中新型 miRNA 的功能评估奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c084/5554241/a2049d5f67e5/41598_2017_8148_Fig1_HTML.jpg

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