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Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours
Spontaneously occurring canine mammary tumours (CMTs) are the most common neoplasms of female unspayed dogs and are of potential importance as models for human breast cancer as well. Mortality rates are thrice higher in dogs as compared to humans with breast cancer, which can partly be attributed to...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202347/ https://www.ncbi.nlm.nih.gov/pubmed/30361548 http://dx.doi.org/10.1038/s41598-018-34097-0 |
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author | Hussain, Shahid Saxena, Sonal Shrivastava, Sameer Arora, Richa Singh, Rajkumar James Jena, Subas Chandra Kumar, Naveen Sharma, Anil Kumar Sahoo, Monalisa Tiwari, Ashok Kumar Mishra, Bishnu Prasad Singh, Raj Kumar |
author_facet | Hussain, Shahid Saxena, Sonal Shrivastava, Sameer Arora, Richa Singh, Rajkumar James Jena, Subas Chandra Kumar, Naveen Sharma, Anil Kumar Sahoo, Monalisa Tiwari, Ashok Kumar Mishra, Bishnu Prasad Singh, Raj Kumar |
author_sort | Hussain, Shahid |
collection | PubMed |
description | Spontaneously occurring canine mammary tumours (CMTs) are the most common neoplasms of female unspayed dogs and are of potential importance as models for human breast cancer as well. Mortality rates are thrice higher in dogs as compared to humans with breast cancer, which can partly be attributed to lack of diagnostic techniques for their early detection. Human breast cancer studies reveal role of autoantibodies in early cancer diagnosis and also the usefulness of autoantibody panels in increasing the sensitivity, as well as, specificity of diagnostic assays. Therefore, in this study, we took advantage of high-throughput Luminex technique for developing a multiplex assay to detect autoantibody signatures against 5 canine mammary tumour-associated autoantigens (TAAs). These TAAs were expressed separately as fusion proteins with halo tag at the N-terminus, which allows easy and specific covalent coupling with magnetic microspheres. The multiplex assay, comprising a panel of candidate autoantigens (TPI, PGAM1, MNSOD, CMYC & MUC1) was used for screening circulating autoantibodies in 125 dog sera samples, including 75 mammary tumour sera and 50 healthy dog sera. The area under curve (AUC) of the combined panel of biomarkers is 0.931 (p < 0.0001), which validates the discriminative potential of the panel in differentiating tumour patients from healthy controls. The assay could be conducted in 3hrs using only 1ul of serum sample and could detect clinical cases of canine mammary tumour with sensitivity and specificity of 78.6% and 90%, respectively. In this study, we report for the first time a multiplexed assay for detection of autoantibodies in canine tumours, utilizing luminex technology and halo-tag coupling strategy. Further to the best of our knowledge, autoantibodies to CMYC and MUC1 have been reported for the first time in canines in this study. |
format | Online Article Text |
id | pubmed-6202347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62023472018-10-29 Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours Hussain, Shahid Saxena, Sonal Shrivastava, Sameer Arora, Richa Singh, Rajkumar James Jena, Subas Chandra Kumar, Naveen Sharma, Anil Kumar Sahoo, Monalisa Tiwari, Ashok Kumar Mishra, Bishnu Prasad Singh, Raj Kumar Sci Rep Article Spontaneously occurring canine mammary tumours (CMTs) are the most common neoplasms of female unspayed dogs and are of potential importance as models for human breast cancer as well. Mortality rates are thrice higher in dogs as compared to humans with breast cancer, which can partly be attributed to lack of diagnostic techniques for their early detection. Human breast cancer studies reveal role of autoantibodies in early cancer diagnosis and also the usefulness of autoantibody panels in increasing the sensitivity, as well as, specificity of diagnostic assays. Therefore, in this study, we took advantage of high-throughput Luminex technique for developing a multiplex assay to detect autoantibody signatures against 5 canine mammary tumour-associated autoantigens (TAAs). These TAAs were expressed separately as fusion proteins with halo tag at the N-terminus, which allows easy and specific covalent coupling with magnetic microspheres. The multiplex assay, comprising a panel of candidate autoantigens (TPI, PGAM1, MNSOD, CMYC & MUC1) was used for screening circulating autoantibodies in 125 dog sera samples, including 75 mammary tumour sera and 50 healthy dog sera. The area under curve (AUC) of the combined panel of biomarkers is 0.931 (p < 0.0001), which validates the discriminative potential of the panel in differentiating tumour patients from healthy controls. The assay could be conducted in 3hrs using only 1ul of serum sample and could detect clinical cases of canine mammary tumour with sensitivity and specificity of 78.6% and 90%, respectively. In this study, we report for the first time a multiplexed assay for detection of autoantibodies in canine tumours, utilizing luminex technology and halo-tag coupling strategy. Further to the best of our knowledge, autoantibodies to CMYC and MUC1 have been reported for the first time in canines in this study. Nature Publishing Group UK 2018-10-25 /pmc/articles/PMC6202347/ /pubmed/30361548 http://dx.doi.org/10.1038/s41598-018-34097-0 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hussain, Shahid Saxena, Sonal Shrivastava, Sameer Arora, Richa Singh, Rajkumar James Jena, Subas Chandra Kumar, Naveen Sharma, Anil Kumar Sahoo, Monalisa Tiwari, Ashok Kumar Mishra, Bishnu Prasad Singh, Raj Kumar Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours |
title | Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours |
title_full | Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours |
title_fullStr | Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours |
title_full_unstemmed | Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours |
title_short | Multiplexed Autoantibody Signature for Serological Detection of Canine Mammary Tumours |
title_sort | multiplexed autoantibody signature for serological detection of canine mammary tumours |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202347/ https://www.ncbi.nlm.nih.gov/pubmed/30361548 http://dx.doi.org/10.1038/s41598-018-34097-0 |
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