Volume 17, Issue 4 pp. 875-883
Original Article

Proteomic profiling of mucosal and submucosal colonic tissues yields protein signatures that differentiate the inflammatory colitides

Amosy E. M'Koma MD, PhD

Corresponding Author

Amosy E. M'Koma MD, PhD

Department of Biochemistry and Cancer Biology, Meharry Medical College, Nashville, Tennessee

Department of General Surgery, Vanderbilt University Medical Center Nashville, Tennessee

Inflammatory Bowel Disease Center, Vanderbilt University Medical Center Nashville, Tennessee

Meharry Medical College School of Medicine, Department of Biochemistry and Cancer Biology, 1005 Dr. D. B. Todd Jr. Blvd., Nashville, TN 37208-3599Search for more papers by this author
Erin H. Seeley PhD

Erin H. Seeley PhD

Mass Spectrometry Research Center, Vanderbilt University Medical Center Nashville, Tennessee

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Mary K. Washington MD, PhD

Mary K. Washington MD, PhD

Inflammatory Bowel Disease Center, Vanderbilt University Medical Center Nashville, Tennessee

Department of Surgical Pathology, Vanderbilt University Medical Center Nashville, Tennessee

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David A. Schwartz MD

David A. Schwartz MD

Inflammatory Bowel Disease Center, Vanderbilt University Medical Center Nashville, Tennessee

Department of Gastroenterology, Vanderbilt University Medical Center Nashville, Tennessee

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Roberta L. Muldoon MD

Roberta L. Muldoon MD

Department of General Surgery, Vanderbilt University Medical Center Nashville, Tennessee

Inflammatory Bowel Disease Center, Vanderbilt University Medical Center Nashville, Tennessee

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Alan J. Herline MD

Alan J. Herline MD

Department of General Surgery, Vanderbilt University Medical Center Nashville, Tennessee

Inflammatory Bowel Disease Center, Vanderbilt University Medical Center Nashville, Tennessee

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Paul E. Wise MD

Paul E. Wise MD

Department of General Surgery, Vanderbilt University Medical Center Nashville, Tennessee

Inflammatory Bowel Disease Center, Vanderbilt University Medical Center Nashville, Tennessee

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Richard M. Caprioli PhD

Richard M. Caprioli PhD

Mass Spectrometry Research Center, Vanderbilt University Medical Center Nashville, Tennessee

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First published: 30 August 2010
Citations: 10

Presented, in part, at the 7th NIH-Network of Research Investigators, Bethesda, MD, April 23–24, 2009; at The American Gastroenterological Association Academic Skills Workshop, Phoenix, AZ, March 13–14, 2009; at The Annual Congress of The American Society of Colon and Rectal Surgeons, Hollywood, FL, May 2–6, 20096 (receiving the “New Jersey Society of Colon and Rectal Surgeons” award for the best basic science presentation); at the Annual Congress of Digestive Disease Week, Chicago, IL, May 30 to June 4, 20097; at the Annual Congress of Digestive Disease Week, New Orleans, LA, May 2–5, 20108; and at the Annual Congress of the American Society of Colon and Rectal Surgeons, Minneapolis, MN, May 15–19, 2010.9

Abstract

Background:

Differentiating ulcerative colitis (UC) from Crohn's colitis (CC) can be difficult and may lead to inaccurate diagnoses in up to 30% of inflammatory bowel disease (IBD) patients. Much of the diagnostic uncertainty arises from the overlap of clinical and histologic features. Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) permits a histology-directed cellular protein analysis of tissues. As a pilot study, we evaluated the ability of histology-directed MALDI-MS to determine the proteomic patterns for potential differences between CC and UC specimens.

Methods:

Mucosal and submucosal layers of CC and UC colon resection samples were analyzed after histologic assessment. To determine whether MALDI-MS would distinguish inflammation, the uninflamed (n = 21) versus inflamed submucosa (n = 22) were compared in UC and the uninflamed (n = 17) versus inflamed submucosa (n = 20) in CC. To determine whether there were proteomic differences between the colitides, the uninflamed UC submucosa (n = 21) was compared versus the uninflamed CC submucosa (n = 17), the inflamed UC submucosa (n = 22) was compared versus the inflamed CC submucosa (n = 20), and inflamed UC mucosa versus inflamed CC mucosa. Pairwise statistics comparisons of the subsets were performed.

Results:

Pairwise comparative analyses of the clinical groups allowed identifying subsets of features important for classification. Comparison of inflamed versus uninflamed CC submucosa showed two significant peaks: m/z 6445 (P = 0.0003) and 12692 (P = 0.003). In the case of inflamed versus uninflamed UC submucosa, several significant differentiating peaks were found, but classification was worse. Comparisons of the proteomic spectra of inflamed submucosa between UC and CC identified two discrete significant peaks: m/z 8773 (P = 0.006) and 9245 (P = 0.0009). Comparisons of the proteomic spectra of uninflamed submucosa between UC and CC identified three discrete significant peaks: m/z 2778 (P = 0.005), 9232 (P = 0.005), and 9519 (P = 0.005). No significantly different features were found between UC and CC inflamed mucosa.

Conclusions:

MALDI-MS was able to distinguish CC and UC specimens while profiling the colonic submucosa. Further analyses and protein identification of the differential protein peaks may aid in accurately diagnosing IBD and developing appropriate personalized therapies. (Inflamm Bowel Dis 2011;)

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