| Literature DB >> 24239682 |
Xiaoli Qu1, Ruiqiang Xie2, Lina Chen3, Chenchen Feng4, Yanyan Zhou5, Wan Li6, Hao Huang7, Xu Jia8, Junjie Lv9, Yuehan He10, Youwen Du11, Weiguo Li12, Yuchen Shi13, Weiming He14.
Abstract
Identifying differences between normal and tumor samples from a modular perspective may help to improve our understanding of the mechanisms responsible for colon cancer. Many cancer studies have shown that signaling transduction and biological pathways are disturbed in disease states, and expression profiles can distinguish variations in diseases. In this study, we integrated a weighted human signaling network and gene expression profiles to select risk modules associated with tumor conditions. Risk modules as classification features by our method had a better classification performance than other methods, and one risk module for colon cancer had a good classification performance for distinguishing between normal/tumor samples and between tumor stages. All genes in the module were annotated to the biological process of positive regulation of cell proliferation, and were highly associated with colon cancer. These results suggested that these genes might be the potential risk genes for colon cancer.Entities:
Keywords: Colon cancer; Module
Mesh:
Year: 2013 PMID: 24239682 DOI: 10.1016/j.ygeno.2013.11.002
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736