Copyright
©The Author(s) 2016.
World J Gastrointest Pathophysiol. Feb 15, 2016; 7(1): 27-37
Published online Feb 15, 2016. doi: 10.4291/wjgp.v7.i1.27
Published online Feb 15, 2016. doi: 10.4291/wjgp.v7.i1.27
Ref. | Bio-sample | Sample size | Proteomic technique | Results |
Meuwis et al[22] | Serum | CD: 30 | SELDI-TOF | 4 candidate proteins selected for high diagnostic value; PF4, MRP8, FIBA, Hpα 2. PF4 and Hpα 2 were also confirmed and correlated using ELISA and immunoblotting |
UC: 30 | ||||
Inflammatory control: 30 | ||||
Healthy controls: 30 | ||||
Kanmura et al[23] | Blood | CD: 22 | SELDI-TOF | Plasma concentrations of HNP1, 2 and 3 were significantly higher in active UC compared to inactive UC, CD and control patients |
UC: 48 | ||||
Colorectal Cancer: 5 | ||||
Infectious colitis: 6 | ||||
Healthy controls: 13 | ||||
Hatsugai et al[24] | Blood | CD: 13 | 2-DE | Multivariate analysis of peripheral blood mononuclear cells protein profile 58 protein) allowed for accurate discrimination between UC and CD |
UC: 17 | MALDI-TOF | |||
Healthy controls: 17 | ||||
Nanni et al[25] | Blood | Healthy controls: 48 | Liquid chromatography quadrupole-TOF | Exopeptidase activity may distinguish CD from UC. Label free method developed could accurately distinguish synthetic spiked samples of serum |
CD: 15 | SELDI-TOF | |||
Sumramanian et al[26] | Serum | CD: 48 | Protein signature of 12 mass: Charge peaks could classify CD with approximately equal 95% sensitivity/specificity | |
UC: 62 | 4 proteins identified as clinically useful | |||
Nanni et al[27] | Serum | Healthy controls: 48 | Solid-phase extraction MALDI-TOF | 20 protein signals could be used to accurately classify IBD patients |
CD: 15 | ||||
UC: 26 | ||||
Vaiopoulou et al[28] | Serum | CD: 24 (12 adults, 12 children) | 2-DE | Clusterin was found to be overexpressed in adult CD. Ceruloplasmin and apolipoprotein B-100 was over-expressed in children |
MALDI-TOF | ||||
Han et al[34] | Intestinal biopsy | CD: 3 | Liquid chromatography quadrupole-TOF | Increased in UC: TTBK2, SYNE2, SUCLG2, POSTN |
UC: 4 | Up-regulated in CD: ANXA2, EPX, LAP3, RDX | |||
Inflammatory polyps: 2 | Up-regulated in IBD: S100A8, MPO, DEFA1B | |||
Up-regulated in CD (P < 0.05 AND > 2x increase): PRG2, LCP1, PSME1 | ||||
Normal colon: 3 | ||||
M’koma et al[35] | Colon samples | CD: 27 | Histology directed MALDI-TOF | 5 m:z peaks were identified and cross-validated for the differentiation of UC and CD |
UC: 24 | ||||
Seeley et al[36] | Colon samples | CD: 26 | Histology directed MALDI-TOF | Using a support vector machine and 25 m:z peaks, UC and CD cases were predicted in 93.3% and 60.4% respectively. A lower spectral accuracy cut-off increased sensitivity |
UC: 36 | ||||
Wasinger et al[39] | Serum | UC: 27 | MRM | SPP24 differentiated IBD patients from healthy controls |
CD: 56 | α-1-microglobulin distinguished patients with UC in remission from healthy controls | |||
Controls: 14 | ||||
RA controls: 12 |
- Citation: Chan PP, Wasinger VC, Leong RW. Current application of proteomics in biomarker discovery for inflammatory bowel disease. World J Gastrointest Pathophysiol 2016; 7(1): 27-37
- URL: https://www.wjgnet.com/2150-5330/full/v7/i1/27.htm
- DOI: https://dx.doi.org/10.4291/wjgp.v7.i1.27