Borkowska Edyta M, Kruk Andrzej, Jedrzejczyk Adam, Rozniecki Marek, Jablonowski Zbigniew, Traczyk Magdalena, Constantinou Maria, Banaszkiewicz Monika, Pietrusinski Michal, Sosnowski Marek, Hamdy Freddie C, Peter Stefan, Catto James W F, Kaluzewski Bogdan
Department of Clinical Genetics, Medical University of Lodz, 3 Sterlinga Street, Lodz, 91-425, Poland; Institute for Cancer Studies and Academic Urology Unit, University of Sheffield, Beech Hill Road, Sheffield, S10 2RX, UK.
Cancer Med. 2014 Oct;3(5):1225-34. doi: 10.1002/cam4.217. Epub 2014 Aug 20.
Kohonen self-organizing maps (SOMs) are unsupervised Artificial Neural Networks (ANNs) that are good for low-density data visualization. They easily deal with complex and nonlinear relationships between variables. We evaluated molecular events that characterize high- and low-grade BC pathways in the tumors from 104 patients. We compared the ability of statistical clustering with a SOM to stratify tumors according to the risk of progression to more advanced disease. In univariable analysis, tumor stage (log rank P = 0.006) and grade (P < 0.001), HPV DNA (P < 0.004), Chromosome 9 loss (P = 0.04) and the A148T polymorphism (rs 3731249) in CDKN2A (P = 0.02) were associated with progression. Multivariable analysis of these parameters identified that tumor grade (Cox regression, P = 0.001, OR.2.9 (95% CI 1.6-5.2)) and the presence of HPV DNA (P = 0.017, OR 3.8 (95% CI 1.3-11.4)) were the only independent predictors of progression. Unsupervised hierarchical clustering grouped the tumors into discreet branches but did not stratify according to progression free survival (log rank P = 0.39). These genetic variables were presented to SOM input neurons. SOMs are suitable for complex data integration, allow easy visualization of outcomes, and may stratify BC progression more robustly than hierarchical clustering.
科霍宁自组织映射(SOM)是一种无监督人工神经网络(ANN),适用于低密度数据可视化。它们能够轻松处理变量之间复杂的非线性关系。我们评估了104例患者肿瘤中表征高级别和低级别BC通路的分子事件。我们比较了统计聚类与SOM根据进展为更晚期疾病的风险对肿瘤进行分层的能力。在单变量分析中,肿瘤分期(对数秩P = 0.006)、分级(P < 0.001)、HPV DNA(P < 0.004)、9号染色体缺失(P = 0.04)以及CDKN2A中的A148T多态性(rs 3731249)(P = 0.02)与进展相关。对这些参数进行多变量分析发现,肿瘤分级(Cox回归,P = 0.001,OR 2.9(95% CI 1.6 - 5.2))和HPV DNA的存在(P = 0.017,OR 3.8(95% CI 1.3 - 11.4))是进展的唯一独立预测因素。无监督层次聚类将肿瘤分组为离散的分支,但未根据无进展生存期进行分层(对数秩P = 0.39)。这些遗传变量被输入到SOM输入神经元。SOM适用于复杂的数据整合,能够轻松直观地呈现结果,并且可能比层次聚类更有力地对BC进展进行分层。