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Identification of differentially expressed genes and fusion genes associated with malignant progression of spinal cord gliomas by transcriptome analysis

机译:通过转录组分析鉴定差异表达基因和脊髓胶质瘤恶性进展相关的融合基因

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摘要

Glioma, the most common histological subtype of primary spinal cord tumors, is considered as a rare central nervous system neoplasm. In this study, 9 glioma samples (4 of grade II and 5 of grade IV with H3K27M positive) were analyzed to examine the molecular mechanisms underlying the malignant progression of gliomas, transcriptome sequencing. Differentially expressed genes (DEGs) in grade IV vs. grade II were analyzed by using the Limma package in R. Enrichment analysis was performed for the individual DEGs through VennPlex software and the Database for Annotation. Gene mutations and fusions were analyzed using the Genome Analysis Toolkit and STAR-Fusion. A total of 416 DEGs were identified in grade IV vs. grade II. Functional analysis of the DEGs showed that GALR1 and GRM5 of neuroactive ligand-receptor interactions signaling pathways may be relaed to malignant progression of gliomas. Further systematic transcriptional profiling identified 11 in-frame/frameshift gene fusions in the tumors. Notably, one novel gene fusions, GATSL2-GTF2I was detected in all of the grade II samples. In summary, the molecular alterations observed in glioma progression may improve the characterization of different human spinal cord glioma grades. The transcriptome analysis of intramedullary spinal cord glioma will provide a new candidate gene list for further mechanism research.
机译:胶质瘤是原发性脊髓瘤的最常见的组织学亚型,被认为是罕见的中枢神经系统肿瘤。在本研究中,分析了9种胶质瘤样品(II级和5级,含有H3K27M阳性的5级)以检查神经瘤的恶性进展,转录组测序的分子机制。通过使用R.在R中的尿玛包来分析IV级Vs级II级的差异表达基因(DEGS)。通过VENNPPLEX软件和数据库进行富集分析进行富集分析。使用基因组分析工具包和恒星分析基因突变和融合。 IV级与II级均确定了416次。对DEG的功能分析表明,神经活性配体 - 受体相互作用信号传导途径的GALR1和GRM5可令对胶质瘤的恶性进展。进一步系统的转录分析鉴定了肿瘤中11个内框架/框架基因融合。值得注意的是,在所有二级样品中检测到一种新的基因融合因子Gatsl2-GTF2i。总之,在胶质瘤进展中观察到的分子改变可以改善不同人脊髓胶质瘤等级的表征。髓内脊髓胶质瘤的转录组分析将为进一步机制研究提供新的候选基因列表。

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