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急性T淋巴细胞性白血病关键基因的筛选与验证

蒋光洁 陈燕华 郭维 张航 邹琳

南方医科大学学报2018,Vol.38Issue(3):261-267,7.
南方医科大学学报2018,Vol.38Issue(3):261-267,7.DOI:10.3969/j.issn.1673-4254.2018.03.04

急性T淋巴细胞性白血病关键基因的筛选与验证

Screening and verification of key genes in T-cell acute lymphoblastic leukemia

蒋光洁 1陈燕华 1郭维 1张航 1邹琳1

作者信息

  • 1. 重庆医科大学附属儿童医院临床分子医学中心//儿童发育疾病研究教育部重点实验室//儿童发育重大疾病国家国际科技合作基地//重庆市干细胞治疗工程技术研究中心,重庆400014
  • 折叠

摘要

Abstract

Objective To explore the key genes in T-cell acute lymphoblastic leukemia(T-ALL)using bioinformatics method to better understand the pathogenic mechanisms of T-ALL. Methods The gene expression profiles of GSE14317 were obtained from Gene Expression Omnibus database.The differentially expressed genes(DEGs)in T-ALL were analyzed using R package Limma. The online analysis tool DAVID was used to perform the functional and pathway enrichment analysis. The protein-protein interaction network was constructed by STRING and visualized by Cytoscape. Based on the JASPAR database, the transcription factors (TFs) of the hub genes were obtained. RT-PCR was used to test the mRNA expression level of the key genes.Results A total of 1443 DEGs were identified,including 800 up-regulated genes and 643 down-regulated genes.These DEGs were significantly enriched in the cell cycle,hematopoietic cell lineage,cytokine-cytokine receptor interaction and T cell receptor signaling pathway.The top 10 hub genes identified from the PPI networks included CDK1,PIK3R1,CCNB1,CCNA2, CDC20, JUN, GNG11, PLK1, PCNA and CCNB2, which were enriched in chemokine signaling pathway, ubiquition mediated proteolysis and cell cycle.In the TF-target gene network,42 differentially expressed TFs were identified,among which ELF5, HIC2 and MEISI had binding sites with 9 of the candidate hub genes.RT-PCR showed that the mRNA expression level of all the candidate hub genes except for GNG11 were consistent with the gene expression profiles. Conclusion The hub genes CDK1,PIK3R1,CCNB1,CCNA2,CDC20,JUN,PLK1,PCNA,CCNB2,ELF5,HIC2 and MEISI participate in the occurrence of T-ALL.Our finding provides new insights into the pathogenesis of T-ALL.

关键词

急性T淋巴细胞白血病/生物信息学/差异表达基因/转录因子

Key words

T-cell acute lymphoblastic leukemia/Bioinformatics analysis/differentially expressed gene/transcription factor

引用本文复制引用

蒋光洁,陈燕华,郭维,张航,邹琳..急性T淋巴细胞性白血病关键基因的筛选与验证[J].南方医科大学学报,2018,38(3):261-267,7.

基金项目

国家自然科学基金(81373444,81570142) Supported by National Natural Science Foundation of China(81373444, 81570142). (81373444,81570142)

南方医科大学学报

OA北大核心CSCDCSTPCDMEDLINE

1673-4254

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