Mining for novel tumor suppressor genes using a shortest path approach

被引:26
|
作者
Chen, Lei [1 ,2 ]
Yang, Jing [3 ,4 ]
Huang, Tao [3 ,4 ]
Kong, Xiangyin [3 ,4 ]
Lu, Lin [5 ]
Cai, Yu-Dong [1 ]
机构
[1] Shanghai Univ, Coll Life Sci, Shanghai 200444, Peoples R China
[2] Shanghai Maritime Univ, Coll Informat Engn, Shanghai 201306, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Inst Hlth Sci, Key Lab Stem Cell Biol, Shanghai 200025, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai 200025, Peoples R China
[5] Columbia Univ, Dept Radiol, Med Ctr, New York, NY 10032 USA
来源
基金
中国国家自然科学基金;
关键词
protein-protein interactions; tumor suppressor genes; shortest path approach; weighted graph; DAVID; NF-KAPPA-B; PROMOTER HYPERMETHYLATION; CANCER SUSCEPTIBILITY; CELL-PROLIFERATION; SIGNALING PATHWAY; PROTEIN FUNCTION; GASTRIC-CANCER; ZINC-FINGERS; EXPRESSION; PREDICTION;
D O I
10.1080/07391102.2015.1042915
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer, being among the most serious diseases, causes many deaths every year. Many investigators have devoted themselves to designing effective treatments for this disease. Cancer always involves abnormal cell growth with the potential to invade or spread to other parts of the body. In contrast, tumor suppressor genes (TSGs) act as guardians to prevent a disordered cell cycle and genomic instability in normal cells. Studies on TSGs can assist in the design of effective treatments against cancer. In this study, we propose a computational method to discover potential TSGs. Based on the known TSGs, a number of candidate genes were selected by applying the shortest path approach in a weighted graph that was constructed using protein-protein interaction network. The analysis of selected genes shows that some of them are new TSGs recently reported in the literature, while others may be novel TSGs.
引用
收藏
页码:664 / 675
页数:12
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