Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/136706
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Type: Journal article
Title: N-glycolylneuraminic acid serum biomarker levels are elevated in breast cancer patients at all stages of disease
Author: Shewell, L.K.
Day, C.J.
Kutasovic, J.R.
Abrahams, J.L.
Wang, J.
Poole, J.
Niland, C.
Ferguson, K.
Saunus, J.M.
Lakhani, S.R.
von Itzstein, M.
Paton, J.C.
Paton, A.W.
Jennings, M.P.
Citation: BMC Cancer, 2022; 22(1):1-11
Publisher: BioMed Central
Issue Date: 2022
ISSN: 1471-2407
1471-2407
Statement of
Responsibility: 
Lucy K. Shewell, Christopher J. Day, Jamie R. Kutasovic, Jodie L. Abrahams, Jing Wang, Jessica Poole, Colleen Niland, Kaltin Ferguson, Jodi M. Saunus, Sunil R. Lakhani, Mark von Itzstein, James C. Paton, Adrienne W. Paton, and Michael P. Jennings
Abstract: Background: Normal human tissues do not express glycans terminating with the sialic acid N-glycolylneuraminic acid (Neu5Gc), yet Neu5Gc-containing glycans have been consistently found in human tumor tissues, cells and secretions and have been proposed as a cancer biomarker. We engineered a Neu5Gc-specifc lectin called SubB2M, and previously reported elevated Neu5Gc biomarkers in serum from ovarian cancer patients using a Surface Plasmon Resonance (SPR)-based assay. Here we report an optimized SubB2M SPR-based assay and use this new assay to analyse sera from breast cancer patients for Neu5Gc levels. Methods: To enhance specifcity of our SPR-based assay, we included a non-sialic acid binding version of SubB, SubBA12, to control for any non-specifc binding to SubB2M, which improved discrimination of cancer-free controls from early-stage ovarian cancer. We analysed 96 serum samples from breast cancer patients at all stages of disease compared to 22 cancer-free controls using our optimized SubB2M-A12-SPR assay. We also analysed a collection of serum samples collected at 6 monthly intervals from breast cancer patients at high risk for disease recurrence or spread. Results: Analysis of sera from breast cancer cases revealed signifcantly elevated levels of Neu5Gc biomarkers at all stages of breast cancer. We show that Neu5Gc serum biomarker levels can discriminate breast cancer patients from cancer-free individuals with 98.96% sensitivity and 100% specifcity. Analysis of serum collected prospectively, postdiagnosis, from breast cancer patients at high risk for disease recurrence showed a trend for a decrease in Neu5Gc levels immediately following treatment for those in remission. Conclusions: Neu5Gc serum biomarkers are a promising new tool for early detection and disease monitoring for breast cancer that may complement current imaging- and biopsy-based approaches.
Keywords: N-glycolylneuraminic acid; Neu5Gc; Biomarker; Breast cancer; Diagnostic; Ovarian cancer
Rights: © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
DOI: 10.1186/s12885-022-09428-0
Grant ID: http://purl.org/au-research/grants/nhmrc/1071659
http://purl.org/au-research/grants/nhmrc/1084050
http://purl.org/au-research/grants/nhmrc/1138466
http://purl.org/au-research/grants/nhmrc/1113867
Published version: http://dx.doi.org/10.1186/s12885-022-09428-0
Appears in Collections:Molecular and Biomedical Science publications

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