Department of Pediatric Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning 530021, China.
Biomed Res Int. 2020 Aug 25;2020:9809347. doi: 10.1155/2020/9809347. eCollection 2020.
We explored the difference in expression of tubulin alpha 1b (TUBA1B) between Wilms' tumor (WT) and normal tissues (NT) from in-house patients and databases, to determine TUBA1B expression in WT and the predictive pathways of coexpressed genes. In-house RNA-sequencing data were performed with WT and NT from three patients from our institute. Other four RNA-sequencing and microarray data were also downloaded from multiple public databases. The TUBA1B expression between WT and NT was analyzed by Student's -test and meta-analysis. The correlation between the expression of TUBA1B and other genes in each study was analyzed. Genes with < 0.05 and > 0.5 were considered as the coexpressing genes of TUBA1B. Overlapping the coexpressed genes of the five studies, including three in-house patients (3 WT 3 NT), GTEx-TARGET (126 WT 51 NT), GSE2172 (18 WT 3 NT), GSE11024 (27 WT 12 NT), and GSE73209 (32 WT 6 NT), were performed with limma and VennDiagram packages in R software. The website of WEB-based GEne SeT AnaLysis toolkit were used to analyze the gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) functional annotations for the overlapped genes. The results showed that the relative expression of TUBA1B in WT tissues from in-house three patients was 280.0086, 141.7589, and 303.8292 and that in NT was 16.5836, 104.8141, and 12.79 (3 WT 3 NT, = 0.0285, ROC = 100%, SMD = 2.74). Student's -test and meta-analysis in all studies revealed that the expression of TUBA1B was upregulated in WT tissues compared to that in NT ( < 0.05, SMD = 2.89, sROC = 0.98). Finally, the research identified the expression of TUBA1B in WT tissues was significantly upregulated than that in NT. The coexpressed genes of TUBA1B were enriched in the pathway of DNA replication, mismatch repair, cell cycle, pathogenic Escherichia coli infection, and spliceosome.
我们探索了来自内部患者和数据库的威尔姆斯瘤(WT)和正常组织(NT)之间微管蛋白α 1b(TUBA1B)表达的差异,以确定 WT 中 TUBA1B 的表达及其共表达基因的预测途径。内部 RNA-seq 数据来自我们研究所的三名患者的 WT 和 NT。还从多个公共数据库下载了另外四个 RNA-seq 和微阵列数据。通过学生 t 检验和荟萃分析分析 WT 和 NT 之间的 TUBA1B 表达。分析了每个研究中 TUBA1B 表达与其他基因的相关性。将表达 < 0.05 和 > 0.5 的基因视为 TUBA1B 的共表达基因。通过 R 软件中的 limma 和 VennDiagram 软件包,对包括来自三名内部患者(3 个 WT 3 个 NT)、GTEx-TARGET(126 个 WT 51 个 NT)、GSE2172(18 个 WT 3 个 NT)、GSE11024(27 个 WT 12 个 NT)和 GSE73209(32 个 WT 6 个 NT)在内的五篇研究的共表达基因进行了重叠分析。使用 WEB 基因集分析工具包网站对重叠基因进行基因本体论(GO)和京都基因与基因组百科全书(KEGG)功能注释分析。结果显示,来自内部三名患者的 WT 组织中 TUBA1B 的相对表达分别为 280.0086、141.7589 和 303.8292,而在 NT 中为 16.5836、104.8141 和 12.79(3 个 WT 3 个 NT, = 0.0285,ROC = 100%,SMD = 2.74)。所有研究的学生 t 检验和荟萃分析表明,WT 组织中 TUBA1B 的表达与 NT 相比上调( < 0.05,SMD = 2.89,sROC = 0.98)。最后,研究确定 WT 组织中 TUBA1B 的表达明显上调。TUBA1B 的共表达基因在 DNA 复制、错配修复、细胞周期、致病性大肠杆菌感染和剪接体途径中富集。