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Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens
Purpose: The purpose of this study is to identify novel urine protein biomarkers of bladder cancer using a Luminex based screening platform. Materials and Methods: The current study examines urine samples from 66 subjects, comprised of 31 Urology clinic controls and 35 bladder cancer patients, using...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057279/ https://www.ncbi.nlm.nih.gov/pubmed/33889301 http://dx.doi.org/10.18632/oncotarget.27941 |
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author | Vanarsa, Kamala Enan, Shereen Patel, Pooja Strachan, Briony Sam Titus, Anto Sam Crosslee Louis Dennis, Aphrihl Lotan, Yair Mohan, Chandra |
author_facet | Vanarsa, Kamala Enan, Shereen Patel, Pooja Strachan, Briony Sam Titus, Anto Sam Crosslee Louis Dennis, Aphrihl Lotan, Yair Mohan, Chandra |
author_sort | Vanarsa, Kamala |
collection | PubMed |
description | Purpose: The purpose of this study is to identify novel urine protein biomarkers of bladder cancer using a Luminex based screening platform. Materials and Methods: The current study examines urine samples from 66 subjects, comprised of 31 Urology clinic controls and 35 bladder cancer patients, using a Luminex based screening platform. ELISA validation was carried out for the top 4 prospective urine biomarkers using an independent cohort of 20 Urology clinic controls and 60 bladder cancer (BC) subjects. Results: Of the 16 proteins screened by Luminex, 10 showed significant elevation in BC compared to the controls. Eight of these urine proteins were able to differentiate BC from control urine with ROC AUC values exceeding 0.70 at p < 0.0001, with specificity values exceeding 0.9. Upon ELISA validation, urine IL-1α, IL-1ra, and IL-8 were able to distinguish control urine from urine drawn from various bladder cancer stages, with IL-8 being the best discriminator. Compared to members of the IL-1 cytokine family, urine IL-8 was also best at discriminating T1 and/or T2–T4 from Ta BC (ROC AUC ≥ 0.83), as well as high grade from low grade BC (ROC AUC ≥ 0.82). Conclusions: These findings suggest that urine IL-1α, IL-1ra and IL-8 are useful indicators of bladder cancer. Urine IL-8 not only distinguishes bladder cancer from controls, it also discriminates high grade from low grade disease, and the successive clinical stages of bladder cancer. While supportive of previous reports, these findings warrant further analysis in prospective cohorts. |
format | Online Article Text |
id | pubmed-8057279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-80572792021-04-21 Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens Vanarsa, Kamala Enan, Shereen Patel, Pooja Strachan, Briony Sam Titus, Anto Sam Crosslee Louis Dennis, Aphrihl Lotan, Yair Mohan, Chandra Oncotarget Research Paper Purpose: The purpose of this study is to identify novel urine protein biomarkers of bladder cancer using a Luminex based screening platform. Materials and Methods: The current study examines urine samples from 66 subjects, comprised of 31 Urology clinic controls and 35 bladder cancer patients, using a Luminex based screening platform. ELISA validation was carried out for the top 4 prospective urine biomarkers using an independent cohort of 20 Urology clinic controls and 60 bladder cancer (BC) subjects. Results: Of the 16 proteins screened by Luminex, 10 showed significant elevation in BC compared to the controls. Eight of these urine proteins were able to differentiate BC from control urine with ROC AUC values exceeding 0.70 at p < 0.0001, with specificity values exceeding 0.9. Upon ELISA validation, urine IL-1α, IL-1ra, and IL-8 were able to distinguish control urine from urine drawn from various bladder cancer stages, with IL-8 being the best discriminator. Compared to members of the IL-1 cytokine family, urine IL-8 was also best at discriminating T1 and/or T2–T4 from Ta BC (ROC AUC ≥ 0.83), as well as high grade from low grade BC (ROC AUC ≥ 0.82). Conclusions: These findings suggest that urine IL-1α, IL-1ra and IL-8 are useful indicators of bladder cancer. Urine IL-8 not only distinguishes bladder cancer from controls, it also discriminates high grade from low grade disease, and the successive clinical stages of bladder cancer. While supportive of previous reports, these findings warrant further analysis in prospective cohorts. Impact Journals LLC 2021-04-13 /pmc/articles/PMC8057279/ /pubmed/33889301 http://dx.doi.org/10.18632/oncotarget.27941 Text en Copyright: © 2021 Vanarsa et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Vanarsa, Kamala Enan, Shereen Patel, Pooja Strachan, Briony Sam Titus, Anto Sam Crosslee Louis Dennis, Aphrihl Lotan, Yair Mohan, Chandra Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens |
title | Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens |
title_full | Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens |
title_fullStr | Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens |
title_full_unstemmed | Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens |
title_short | Urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens |
title_sort | urine protein biomarkers of bladder cancer arising from 16-plex antibody-based screens |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8057279/ https://www.ncbi.nlm.nih.gov/pubmed/33889301 http://dx.doi.org/10.18632/oncotarget.27941 |
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