Comprehensive Quantitative Analysis of Ovarian and Breast Cancer Tumor Peptidomes

被引:22
作者
Xu, Zhe [1 ]
Wu, Chaochao [1 ]
Xie, Fang [1 ]
Slysz, Gordon W. [1 ]
Tolic, Nikola [2 ]
Monroe, Matthew E. [1 ]
Petyuk, Vladislav A. [1 ]
Payne, Samuel H. [1 ]
Fujimoto, Grant M. [1 ]
Moore, Ronald J. [1 ]
Fillmore, Thomas L. [2 ]
Schepmoes, Athena A. [1 ]
Levine, Douglas A. [3 ]
Townsend, R. Reid [4 ]
Davies, Sherri R. [4 ]
Li, Shunqiang [4 ]
Ellis, Matthew [4 ]
Boja, Emily [5 ]
Rivers, Robert [5 ]
Rodriguez, Henry [5 ]
Rodland, Karin D. [1 ]
Liu, Tao [1 ]
Smith, Richard D. [1 ]
机构
[1] Pacific NW Natl Lab, Div Biol Sci, Richland, WA 99354 USA
[2] Pacific NW Natl Lab, Environm Mol Sci Lab, Richland, WA 99354 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Surg, Gynecol Serv, New York, NY 10065 USA
[4] Washington Univ, Dept Med, St Louis, MO 63130 USA
[5] NCI, Off Canc Clin Prote Res, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
protein degradation; peptidomics; proteases; tumor; ovarian cancer; breast cancer; ischemia; MOLECULAR-WEIGHT PROTEOME; SOFTWARE PACKAGE; ACCURATE MASS; PROTEASOME; SERUM; METHIONINE; NEUROPEPTIDES; STABILITY;
D O I
10.1021/pr500840w
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aberrant degradation of proteins is associated with many pathological states, including cancers. Mass spectrometric analysis of tumor peptidomes, the intracellular and intercellular products of protein degradation, has the potential to provide biological insights on proteolytic processing in cancer. However, attempts to use the information on these smaller protein degradation products from tumors for biomarker discovery and cancer biology studies have been fairly limited to date, largely due to the lack of effective approaches for robust peptidomics identification and quantification and the prevalence of confounding factors and biases associated with sample handling and processing. Herein, we have developed an effective and robust analytical platform for comprehensive analyses of tissue peptidomes, which is suitable for high-throughput quantitative studies. The reproducibility and coverage of the platform, as well as the suitability of clinical ovarian tumor and patient-derived breast tumor xenograft samples with postexcision delay of up to 60 min before freezing for peptidomics analysis, have been demonstrated. Moreover, our data also show that the peptidomics profiles can effectively separate breast cancer subtypes, reflecting tumor-associated protease activities. Peptidomics complements results obtainable from conventional bottom-up proteomics and provides insights not readily obtainable from such approaches.
引用
收藏
页码:422 / 433
页数:12
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