Ovarian cancer detection by logical analysis of proteomic data

被引:73
作者
Alexe, G
Alexe, S
Liotta, LA
Petricoin, E
Reiss, M
Hammer, PL
机构
[1] Rutgers State Univ, Rutgers Ctr Operat Res, RUTCOR, Piscataway, NJ 08854 USA
[2] NCI, Pathol Lab, NIH, Bethesda, MD 20892 USA
[3] US FDA, Ctr Biol Evaluat & Res, NIH, Clin Proteom Program,Dept Therapeut, Bethesda, MD 20014 USA
[4] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Inst Canc, Dept Med, New Brunswick, NJ USA
关键词
logical analysis of data; ovarian cancer;
D O I
10.1002/pmic.200300574
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new type of efficient and accurate proteomic ovarian cancer diagnosis systems is proposed. The system is developed using the combinatorics and optimization-based methodology of logical analysis of data (LAD) to the Ovarian Dataset 8-7-02 (http://clinicalproteomics.steem.com), which updates the one used by Petricoin et al, in The Lancet 2002, 359, 572-577. This mass spectroscopy-generated dataset contains expression profiles of 15154 peptides defined by their mass/charge ratios (m/z) in serum of 162 ovarian cancer and 91 control cases. Several fully reproducible models using only 7-9 of the 15 154 peptides were constructed, and shown in multiple cross-validation tests (k-folding and leave-one-out) to provide sensitivities and specificities of up to 100%. A special diagnostic system for stage I ovarian cancer patients is shown to have similarly high accuracy. Other results: (i) expressions of peptides with relatively low m/z values in the dataset are shown to be better at distinguishing ovarian cancer cases from controls than those with higher m/z values; (ii) two large groups of patients with a high degree of similarities among their formal (mathematical) profiles are detected; (iii) several peptides with a blocking or promoting effect on ovarian cancer are identified.
引用
收藏
页码:766 / 783
页数:18
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