Network-Based Differential Analysis to Identify Molecular Features of Tumorigenesis for Esophageal Squamous Carcinoma.
Network-Based Differential Analysis to Identify Molecular Features of Tumorigenesis for Esophageal Squamous Carcinoma.
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基于网络的差异分析识别食管鳞癌肿瘤发生的分子特征
DOI:
10.3390/molecules23010088
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发表时间:
2018-01-01
期刊:
影响因子:
--
通讯作者:
Pan L
中科院分区:
文献类型:
--
作者:
Jiang S;Zhang Q;Su Y;Pan L
Esophageal cancer has a poor prognosis and high mortality rate across the world. The diagnosis and treatment of esophageal cancer are hindered by the limited knowledge about the pathogenesis mechanisms of esophageal cancer. Esophageal cancer has two major subtypes, squamous and adenocarcinoma. In this work, we proposed a method to select candidate biomarkers of esophageal squamous carcinoma based on the topological differential analysis between the gene–gene interaction networks for esophageal squamous carcinoma and normal cells. We established the gene–gene interaction networks for esophageal squamous carcinoma and normal based on the correlation of genes. For each gene, we firstly calculated and compared five centrality measures, which could reflect the topological property of a network. According to five centrality measures, the genes with large differences between the two networks were regarded as candidate biomarkers for esophageal squamous carcinoma. A total of 21 candidate biomarkers were identified for esophageal squamous carcinoma, and seven of them have been confirmed to be biomarkers of esophageal-12 squamous carcinoma by previous research. In addition, six genes (RBPMS2, PDK4, IGK, SBSN, IFIT3 and HSPB6) were likely to be the biomarkers of tumorigenesis for esophageal squamous carcinoma due to the fact that the biological processes in which they participate are closely related with the development of esophageal squamous carcinoma. Statistical analysis indicates that effectiveness of the detected biomarkers of esophageal squamous carcinoma. The proposed method could be extended to other complex diseases for detecting the molecular features of pathopoiesis and targets for targeted therapy.
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DOI:
10.12659/msm.897663
发表时间:
2016-10-23
期刊:
Medical science monitor : international medical journal of experimental and clinical research
影响因子:
--
作者:
Han Q;Zhang HY;Zhong BL;Wang XJ;Zhang B;Chen H
通讯作者:
Chen H
影响因子:
14.9
作者:
Kim MY;Koh DI;Choi WI;Jeon BN;Jeong DY;Kim KS;Kim K;Kim SH;Hur MW
通讯作者:
Hur MW
影响因子:
4.7
作者:
Li, Z;Szabolcs, M;Efstratiadis, A
通讯作者:
Efstratiadis, A
影响因子:
28.2
作者:
Esteller M;Pandolfi PP
通讯作者:
Pandolfi PP
DOI:
10.1158/1055-9965.epi-13-1329
发表时间:
2014-08
期刊:
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
影响因子:
--
作者:
Li WQ;Hu N;Burton VH;Yang HH;Su H;Conway CM;Wang L;Wang C;Ding T;Xu Y;Giffen C;Abnet CC;Goldstein AM;Hewitt SM;Taylor PR
通讯作者:
Taylor PR