College of Bioinformatics Science and Technology, Harbin Medical University,Harbin,Hei Longjiang Province, China.
PLoS One. 2014 Mar 18;9(3):e92395. doi: 10.1371/journal.pone.0092395. eCollection 2014.
Gene expression profiles have drawn broad attention in deciphering the pathogenesis of human cancers. Cancer-related gene modules could be identified in co-expression networks and be applied to facilitate cancer research and clinical diagnosis. In this paper, a new method was proposed to identify lung cancer-risk modules and evaluate the module-based disease risks of samples. The results showed that thirty one cancer-risk modules were closely related to the lung cancer genes at the functional level and interactional level, indicating that these modules and genes might synergistically lead to the occurrence of lung cancer. Our method was proved to have good robustness by evaluating the disease risk of samples in eight cancer expression profiles (four for lung cancer and four for other cancers), and had better performance than the WGCNA method. This method could provide assistance to the diagnosis and treatment of cancers and a new clue for explaining cancer mechanisms.
基因表达谱在解析人类癌症发病机制方面引起了广泛关注。在共表达网络中可以识别与癌症相关的基因模块,并将其应用于促进癌症研究和临床诊断。本文提出了一种新的方法来识别肺癌风险模块,并评估基于模块的样本疾病风险。结果表明,三十一个癌症风险模块在功能和交互水平上与肺癌基因密切相关,表明这些模块和基因可能协同导致肺癌的发生。通过评估八个癌症表达谱(四个肺癌和四个其他癌症)中样本的疾病风险,证明了我们的方法具有良好的稳健性,并且比 WGCNA 方法具有更好的性能。该方法可以为癌症的诊断和治疗提供帮助,并为解释癌症机制提供新线索。