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Published in: Pathology & Oncology Research 3/2015

01-07-2015 | Research

Identification of Key Genes Associated with Colorectal Cancer Based on the Transcriptional Network

Authors: Guoting Chen, Hengping Li, Xianping Niu, Guofeng Li, Ning Han, Xin Li, Guang Li, Yangzhou Liu, Guixin Sun, Yong Wang, Zengchun Li, Qinchuan Li

Published in: Pathology & Oncology Research | Issue 3/2015

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Abstract

Colorectal cancer (CRC) is among the most lethal human cancers, but the mechanism of the cancer is still unclear enough. We aimed to explore the key genes in CRC progression. The gene expression profile (GSE4183) of CRC was obtained from Gene Expression Omnibus database which included 8 normal samples, 15 adenoma samples, 15 CRC samples and 15 inflammatory bowel disease (IBD) samples. Thereinto, 8 normal, 15 adenoma, and 15 CRC samples were chosen for our research. The differentially expressed genes (DEGs) in normal vs. adenoma, normal vs. CRC, and adenoma vs. CRC, were identified using the Wilcoxon test method in R respectively. The interactive network of DEGs was constructed to select the significant modules using the Pearson’s correlation. Meanwhile, transcriptional network of DEGs was also constructed using the g: Profiler. Totally, 2,741 DEGs in normal vs. adenoma, 1,484 DEGs in normal vs. CRC, and 396 DEGs in adenoma vs. CRC were identified. Moreover, function analysis of DEGs in each group showed FcR-mediated phagocytosis pathway in module 1, cardiac muscle contraction pathway in module 6, and Jak-STAT signaling pathway in module 19 were also enriched. Furthermore, MZF1 and AP2 were the transcription factor in module 6, with the target SP1, while SP1 was also a transcription in module 20. DEGs like NCF1, AKT, SP1, AP2, MZF1, and TPM might be used as specific biomarkers in CRC development. Therapy targeting on the functions of these key genes might provide novel perspective for CRC treatment.
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Metadata
Title
Identification of Key Genes Associated with Colorectal Cancer Based on the Transcriptional Network
Authors
Guoting Chen
Hengping Li
Xianping Niu
Guofeng Li
Ning Han
Xin Li
Guang Li
Yangzhou Liu
Guixin Sun
Yong Wang
Zengchun Li
Qinchuan Li
Publication date
01-07-2015
Publisher
Springer Netherlands
Published in
Pathology & Oncology Research / Issue 3/2015
Print ISSN: 1219-4956
Electronic ISSN: 1532-2807
DOI
https://doi.org/10.1007/s12253-014-9880-9

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