Discrimination analysis of mass spectrometry proteomics for ovarian cancer detection

被引:12
作者
Hong Y.-J. [1 ]
Wang X.-D. [1 ]
Shen D. [2 ]
Zeng S. [1 ]
机构
[1] College of Pharmaceutical Sciences, Zhejiang University
[2] Alps Biostatistics Services LLC, Philadelphia, PA
关键词
Discrimination analysis; Mass spectrometry; Ovarian cancer; Proteomics;
D O I
10.1111/j.1745-7254.2008.00861.x
中图分类号
学科分类号
摘要
Aim: A discrimination analysis has been explored for the probabilistic classification of healthy versus ovarian cancer serum samples using proteomics data from mass spectrometry (MS). Methods: The method employs data normalization, clustering, and a linear discriminant analysis on surface-enhanced laser desorption ionization (SELDI) time-of-flight MS data. The probabilistic classification method computes the optimal linear discriminant using the complex human blood serum SELDI spectra. Cross-validation and training/testing data-split experiments are conducted to verify the optimal discriminant and demonstrate the accuracy and robustness of the method. Results: The cluster discrimination method achieves excellent performance. The sensitivity, specificity, and positive predictive values are above 97% on ovarian cancer. The protein fraction peaks, which significantly contribute to the classification, can be available from the analysis process. Conclusion: The discrimination analysis helps the molecular identities of differentially expressed proteins and peptides between the healthy and ovarian patients. © 2008 CPS and SIMM.
引用
收藏
页码:1240 / 1246
页数:6
相关论文
共 18 条
  • [1] Liotta L.A., Ferrari M., Petricoin E., Clinical proteomics: Written in blood, Nature, 425, (2003)
  • [2] Rai A.J., Chan D.W., Cancer proteomics: Serum diagnostics for tumor marker discovery, Ann N Y Acad Sci, 1022, pp. 286-94, (2004)
  • [3] Diamandis E.P., Analysis of serum proteomic patterns for early cancer diagnosis: Drawing attention to potential problems, J Natl Cancer Inst, 96, pp. 353-6, (2004)
  • [4] Ransohoff D.F., Lessons from controversy: Ovarian cancer screening and serum proteomics, J Natl Cancer Inst, 97, pp. 315-9, (2005)
  • [5] Colantonio D.A., Chan D.W., The clinical application of proteomics, Clin Chim Acta, 357, pp. 151-8, (2005)
  • [6] Diamandis E.P., Mass spectrometry as a diagnostic and a cancer biomarker discovery tool: Opportunities and potential limitations, Mol Cell Proteomics, 3, pp. 367-78, (2004)
  • [7] Aebersold R., Mann M., Mass spectrometry-based proteomics, Nature, 422, pp. 198-207, (2003)
  • [8] Pusch W., Flocco M.T., Leung S., Thiele H., Kostrzewa M., Mass spectrometry-based clinical proteomics, Pharmacogenomics, 4, pp. 463-76, (2003)
  • [9] Diamandis E.P., Van Der Merwe D., Plasma protein profiling by mass spectrometry for cancer diagnosis: Opportunities and limitations, Clin Cancer Res, 11, pp. 963-5, (2005)
  • [10] Soltys S.G., Le Q.T., Shi G., Tibshirani R., Giaccia A.J., Koong A.C., The use of plasma surface-enhanced laser desorption/ionization time-of-flight mass spectrometry proteomic patterns for detection of head and neck squamous cell cancers, Clin Cancer Res, 10, pp. 4806-12, (2004)