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Supplementary_material: Prognostic significance and function of minichromosome maintenance protein 10 in human hepatocellular carcinoma.docx

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<b>Supplementary Figure 1</b> <b>Data for MCM10 expression in HCC from online databases.</b> (<b>A</b>) The transcription level of MCM10 in 20 different types of human cancers (ONCOMINE). Color is determined by the highest gene rank percentile genes based on log fold-change; red represents upregulation and blue indicates downregulation. Cut-off of <i>P</i>-value and fold change were as following: <i>P</i>-value: 0.05, fold change: 1.5, gene rank: 10%, data type: mRNA. (<b>B</b>) Relative expression of MCM10 in HCC tissues (n = 371) and adjacent normal liver tissues (n = 50) from TCGA database (UALCAN). (<b>C</b>) Relative expression of MCM10 in normal individuals (n = 50) and in HCC patients with different cancer stages (Stage 1, n = 168; Stage 2, n = 84; Stage 3, n = 82; Stage 4, n = 6). *<i>P</i> &lt; 0.05, **<i>P</i> &lt; 0.01, ***<i>P</i> &lt; 0.001. (<b>D</b>) Representative immunohistochemistry images of MCM10 protein in HCC tissues and normal liver tissues (Human Protein Atlas). <b> </b> <b>Supplementary Table 1 </b> Clinicopathological characteristics of 364 HCC patients. <b>Supplementary Table 2 </b> Estimated AUC value of TNM and MCM10 in 364 HCC patients after follow-up. <b>Supplementary Table 3 </b> Summary of significantly enriched GO annotations of MCM10 related network.

<b>补充图1</b> <b>肝细胞癌(HCC)中MCM10表达的在线数据库数据</b>。(<b>A</b>) MCM10在20种不同类型人类癌症中的转录水平(ONCOMINE数据库)。颜色由基于对数倍数变化的最高基因排名百分位基因决定;红色代表上调,蓝色代表下调。<i>P</i>值和倍数变化的cutoff值设置如下:<i>P</i>值:0.05,倍数变化:1.5,基因排名:10%,数据类型:mRNA。(<b>B</b>) 来自TCGA数据库(UALCAN平台)的肝细胞癌(HCC)组织(n=371)与癌旁正常肝组织(n=50)中MCM10的相对表达水平。(<b>C</b>) 正常个体(n=50)与不同分期肝细胞癌(HCC)患者(1期:168例;2期:84例;3期:82例;4期:6例)中MCM10的相对表达水平。*<i>P</i> < 0.05,**<i>P</i> < 0.01,***<i>P</i> < 0.001。(<b>D</b>) 肝细胞癌(HCC)组织与正常肝组织中MCM10蛋白的代表性免疫组化图像(人类蛋白质图谱数据库)。 <b>补充表1</b> 364例肝细胞癌(HCC)患者的临床病理特征。 <b>补充表2</b> 364例肝细胞癌(HCC)患者随访后TNM分期与MCM10的估计AUC值。 <b>补充表3</b> MCM10相关网络显著富集的基因本体(GO)注释总结。
提供机构:
Taylor & Francis
创建时间:
2021-08-05
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