Detecting glycan cancer biomarkers in serum samples using MALDI FT-ICR mass spectrometry data

被引:31
作者
Barkauskas, Donald A. [1 ]
An, Hyun Joo [2 ]
Kronewitter, Scott R. [2 ]
de Leoz, Maria Lorna [2 ]
Chew, Helen K. [3 ]
de Vere White, Ralph W. [4 ]
Leiserowitz, Gary S. [5 ]
Miyamoto, Suzanne [3 ]
Lebrilla, Carlito B. [2 ]
Rocke, David M. [6 ]
机构
[1] Univ Calif Davis, Sch Med, Grad Grp Biostat Designated Emphasis Biotechnol, Davis, CA 95616 USA
[2] Univ Calif Davis, Sch Med, Dept Chem, Davis, CA 95616 USA
[3] Univ Calif Davis, Sch Med, Ctr Canc, Div Hematol Oncol, Davis, CA 95616 USA
[4] Univ Calif Davis, Sch Med, Ctr Canc, Div Urol, Davis, CA 95616 USA
[5] Univ Calif Davis, Sch Med, Ctr Canc, Div Gynecol Oncol, Davis, CA 95616 USA
[6] Univ Calif Davis, Sch Med, Div Biostat, Davis, CA 95616 USA
基金
美国国家卫生研究院;
关键词
N-GLYCOLYLNEURAMINIC ACID; OVARIAN-CANCER; CELL-SURFACE; BIOSYNTHESIS; DISCOVERY;
D O I
10.1093/bioinformatics/btn610
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: The development of better tests to detect cancer in its earliest stages is one of the most sought-after goals in medicine. Especially important are minimally invasive tests that require only blood or urine samples. By pro. ling oligosaccharides cleaved from glycosylated proteins shed by tumor cells into the blood stream, we hope to determine glycan profiles that will help identify cancer patients using a simple blood test. The data in this article were generated using matrix-assisted laser desorption/ionization Fourier transform ion cyclotron resonance mass spectrometry (MALDI FT-ICR MS). We have developed novel methods for analyzing this type of mass spectrometry data and applied it to eight datasets from three different types of cancer (breast, ovarian and prostate). Results: The techniques we have developed appear to be effective in the analysis of MALDI FT-ICR MS data. We found significant differences between control and cancer groups in all eight datasets, including two structurally related compounds that were found to be significantly different between control and cancer groups in all three types of cancer studied.
引用
收藏
页码:251 / 257
页数:7
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