Artificial neural networks and decision tree model analysis of liver cancer proteomes

被引:37
作者
Luk, John M.
Lam, Brian Y.
Lee, Nikki P. Y.
Ho, David W.
Sham, Pak C.
Chen, Lei
Peng, Jirun
Leng, Xisheng
Day, Philip J.
Fan, Sheung-Tat
机构
[1] Univ Hong Kong, Fac Med, Dept Surg, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Fac Med, Ctr Canc Res, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Genome Res Ctr, Hong Kong, Hong Kong, Peoples R China
[4] Univ Hong Kong, Dept Psychiat, Hong Kong, Hong Kong, Peoples R China
[5] Peking Univ, Peoples Hosp, Dept Surg, Beijing 100871, Peoples R China
[6] Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester, Lancs, England
关键词
cancer proteome; classification; CART; ANN; hepatocellular carcinoma;
D O I
10.1016/j.bbrc.2007.06.172
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
Hepatocellular carcinoma (HCC) is a heterogeneous cancer and usually diagnosed at late advanced tumor stages of high lethality. The present study attempted to obtain a proteome-wide analysis of HCC in comparison with adjacent non-tumor liver tissues, in order to facilitate biomarkers' discovery and to investigate the mechanisms of HCC development. A cohort of 66 Chinese patients with HCC was included for proteomic profiling study by two-dimensional gel electrophoresis (2-DE) analysis. Artificial neural network (ANN) and decision tree (CART) data-mining methods were employed to analyze the profiling data and to delineate significant patterns and trends for discriminating HCC from non-malignant liver tissues. Protein markers were identified by tandem MS/MS. A total of 132 proteome datasets were generated by 2-DE expression profiling analysis, and each with 230 consolidated protein expression intensities. Both the data-mining algorithms successfully distinguished the HCC phenotype from other non-malignant liver samples. The detection sensitivity and specificity of ANN were 96.97% and 87.88%, while those of CART were 81.82% and 78.79%, respectively. The three biological classifiers in the CART model were identified as cytochrome b5, heat shock 70 kDa protein 8 isoform 2, and cathepsin B. The 2-DE-based proteomic profiling approach combined with the ANN or CART algorithm yielded satisfactory performance on identifying HCC and revealed potential candidate cancer biomarkers. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:68 / 73
页数:6
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