Integrated Analysis of Oncogenic Networks in Colorectal Cancer Identifies GUCA2A as a Molecular Marker

Zhang, Hui; Du, Yuanyuan; Wang, Zhuo; Lou, Rui; Wu, Jianzhong; Feng, Jifeng

Integrated Analysis of Oncogenic Networks in Colorectal Cancer Identifies GUCA2A as a Molecular Marker

2019

Zhang, Hui(Research Center for Clinical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University) | Du, Yuanyuan(Research Center for Clinical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University) | Wang, Zhuo(Research Center for Clinical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University) | Lou, Rui(Department of Oncology, The Affiliated Hospital of Jiangnan University) | Wu, Jianzhong(Research Center for Clinical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University) | Feng, Jifeng(Research Center for Clinical Oncology, The Affiliated Cancer Hospital of Nanjing Medical University)

Colorectal cancer (CRC) is one of the most common and deadly malignancies in the world. In China, the morbidity rate of CRC has increased during the period 2000 to 2011. Biomarker detection for early CRC diagnosis can effectively reduce the mortality of patients with CRC. To explore the underlying mechanisms of effective biomarkers and identify more of them, we performed weighted correlation network analysis (WGCNA) on a GSE68468 dataset generated from 378 CRC tissue samples. We screened the gene set (module), which was significantly associated with CRC histology, and analyzed the hub genes. The key genes were identified by obtaining six colorectal raw data (i.e., GSE25070, GSE44076, GSE44861, GSE21510, GSE9348, and GSE21815) from the GEO database (https://www.ncbi.nlm.nih.gov/geo). The robust differentially expressed genes (DEGs) in all six datasets were calculated and obtained using the library “RobustRankAggreg” package in R 3.5.1. An integrated analysis of CRC based on the top 50 downregulated DEGs and hub genes in the red module from WGCNA was conducted, and the intersecting genes were screened. The Kaplan–Meier plot was further analyzed, and the genes associated with CRC prognosis based on patients from the TCGA database were determined. Finally, we validated the candidate gene in our clinical CRC specimens. We postulated that the candidate genes screened from the database and verified by our clinical pathological data may contribute to understanding the molecular mechanisms of tumorigenesis and may serve as potential biomarkers for CRC diagnosis and treatment.

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