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基于生物信息学分析筛选宫颈癌进展中的关键基因 被引量:1

Identification of key genes in cervical cancer progression by integrated bioinformatics analysis
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摘要 目的:通过生物信息学分析的方法,筛选宫颈癌进展中的关键基因,寻找潜在的分子标志物和治疗靶点。方法:在GEO(Gene Expression Omnibus)数据库中检索宫颈癌进展相关的mRNA和miRNA基因芯片数据,借助GEO2R分析差异表达基因(DEG)和差异表达miRNA(DEM),进行富集分析以及构建蛋白质-蛋白质相互作用(PPI)网络和miRNA-靶基因调控网络。结果:共筛选出250个DEG和166个DEM,并构建出由123个节点(node)和283项互相作用(edge)构成的PPI网络以及由66个节点和137个相互作用构成的miRNA-靶基因调控网络。经分析,ATAD2、SMC4和POLQ基因不仅是筛选出的表达上调的DEG,而且是PPI网络中枢纽蛋白的编码基因,并在miRNA-靶基因调控网络中同时受DEM—miR-20A、miR-20B、miR-106B和miR-17-5P的调控。结论:ATAD2、SMC4和POLQ基因可能在宫颈癌进展过程中发挥着重要作用。 Objective:To identify the key genes in cervical cancer progression by integrated bioinformatics analysis to search for potential biomarkers and therapeutic targets.Methods:The mRNA and miRNA microarray datasets related to the progression of cervical cancer were searched on the GEO(the Gene Expression Omnibus)database and differentially expressed gene(DEG)and differentially expressedmiRNA(DEM)were analyzed by GEO2R.Then,the functional enrichment analyses,protein-protein interaction(PPI)network and miRNA-target regulatory network construction were conducted.Results:Totally,250 DEGs and 166 DEMs in the progression of cervical cancer were screened out,and a PPI network composed of 123 nodes and 283 edges and a miRNA-target regulatory network composed of 66 nodes and 137 edges were constructed.Based on a series of analyses,the genes ATAD2,SMC4 and POLQ were not only identified as the overexpressed DEGs,but also the coding genes of hub proteins in the PPI network and regulated by the DEMs,miR-20A,miR-20B,miR-106B and miR-17-5P in the miRNA-target gene regulatory network.Conclusion:ATAD2,SMC4 and POLQ genes may play important roles in the progression of cervical cancer.
作者 刘玉林 臧玉琴 王颖梅 薛凤霞 LIU Yu-lin;ZANG Yu-qin;WANG Ying-mei;XUE Feng-xia(Department of Gynecology and Obstetrics,The General Hospital,Tianjin Medical University;Tianjin Key Laboratory of Female Reproductive Health and Eugenics,Tianjin 300052,China)
出处 《天津医科大学学报》 2022年第1期8-14,共7页 Journal of Tianjin Medical University
基金 国家自然科学基金(81972448) 天津市科委基金(20JCZDJC00330)。
关键词 宫颈癌 生物信息学分析 差异表达基因 差异表达miRNA 蛋白质-蛋白质相互作用网络 miRNA-靶基因调控网络 cervical cancer bioinformatics analysis differentially expressed gene differentially expressed miRNA protein-protein interaction network miRNA-target regulatory network
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  • 1Arbyn M, Castelisague X, de Sanjose S, Bruni L, Saraiya M, Bray F, et al. Worldwide burden of cervical cancer in 2008. Ann Oncol 2011; 22: 2675-2686.
  • 2Kim VN, Han J, Siomi MC. Biogenesis of small RNAs in animals. Nat Rev Mol Cell Biol 2009; 10: 126-139.
  • 3Bartel DP. MicroRNAs: target recognition and regulatory functions. Cell 2009; 136: 215-233.
  • 4Calin GA, Dumitru CD, Shimizu M, Bichi R, Zupo S, Noch E, et al. Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia. Proc Natl Acad Sci USA 2002; 99: 15524-15529.
  • 5Rao Q, Zhou H, Peng Y, Li J, Lin Z. Aberrant microRNA expression in human cervical carcinomas. Med Oncol 2012; 29: 1242-1248.
  • 6Hudelist G, Czerwenka K, Singer C, Pischinger K, Kubista E, Manavi M. cDNA array analysis of cytobrush-collected normal and malignant cervical epithelial cells: a feasibility study. Cancer Genet Cytogenet 2005; 158: 35-42.
  • 7Wright GW, Simon RM. A random variance model for detection of differential gene expression in small microarray experiments. Bioinformatics 2003; 19: 2448-2455.
  • 8Dupuy D, Bertin N, Hidalgo CA, Venkatesan K, Tu D, Lee D, et al. Genome-scale analysis of in vivo spatiotemporal promoter activity in Caenorhabditis elegans. Nat Biotechnol 2007; 25: 663-668.
  • 9Yi M, Horton JD, Cohen JC, Hobbs HH, Stephens RM. WholePathwayScope: a comprehensive pathway-based analysis tool for high-throughput data. BMC Bioinformatics 2006; 7: 30.
  • 10Kanehisa M, Goto S, Kawashima S, Okuno Y, Hattori M. The KEGG resource for deciphering the genome. Nucleic Acids Res 2004: 32: D277-D280.

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