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Profiling of isomer-specific IgG N-glycosylation in cohort of Chinese colorectal cancer patients.
Biochimica et Biophysica Acta (BBA) - General Subjects ( IF 3 ) Pub Date : 2019-12-27 , DOI: 10.1016/j.bbagen.2019.129510
Si Liu 1 , Zhiwen Huang 1 , Qiwei Zhang 2 , Yang Fu 1 , Liming Cheng 3 , Bi-Feng Liu 1 , Xin Liu 1
Affiliation  

BACKGROUD Given the increasing morbidity and mortality of colorectal cancer (CRC), it is urgent to develop a noninvasive screening strategy for early diagnosis of CRC. Altered IgG glycosylation is associated with CRC progression, whereas the association of IgG isomeric glycosylation with CRC were not investigated. METHODS Methylamidation of IgG N-glycans was conducted prior to PGC-based nanoLC-ESI-MS/MS analysis. Data processing was operated by a self-developed application based on MATLAB solution. Statistical analysis including K-S test, t-test, ROC curve and OPLS-DA were successively performed. Additionally, an independent set was utilized to validate the results. RESULTS Total 28 IgG glycans and 79 compositional isomers were identified, over half of which are firstly identified so far. Statistical analysis showed that CRC associates with increase in IgG agalactosylation, decrease in IgG sialylation and fucosylation of sialylated glycans. Additionally, it was found that three compositional isomers (H3N4F1-a, H3N4F1-b and H4N3S1F1-e) could distinguish CRC and early stages from controls with an accurate area under the receiver operating characteristic curve. Significantly, these results were validated in an independent set by multivariate statistical analysis. CONCLUSIONS This is the first comprehensively profiling of isomer-specific IgG N-glycosylation, which could differentiate normal controls from colorectal disease patients. The candidate IgG glyco-biomarkers provide important screening indicators for early diagnosis of CRC. GENERAL SIGNIFICANCE Colorectal cancer progression is strongly associated with isomer-specific IgG N-glycosylation.
更新日期:2019-12-27
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