Proteomic profiling of urine for the detection of colon cancer

<p>Abstract</p> <p>Background</p> <p>Colorectal cancer is the second most common cause of cancer related death in the developed world. To date, no blood or stool biomarkers with both high sensitivity and specificity for potentially curable early stage disease have been...

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Main Authors: Wakelam Michael JO, Steven Neil, Tselepis Chris, Wei Wenbin, Hamilton Emma, Joy Howard, Nyangoma Stephen, Ward Douglas G, Johnson Philip J, Ismail Tariq, Martin Ashley
Format: Article
Language:English
Published: BMC 2008-06-01
Series:Proteome Science
Online Access:http://www.proteomesci.com/content/6/1/19
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spelling doaj-96d401bce0f74cef91371160850f9f8a2020-11-24T20:53:40ZengBMCProteome Science1477-59562008-06-01611910.1186/1477-5956-6-19Proteomic profiling of urine for the detection of colon cancerWakelam Michael JOSteven NeilTselepis ChrisWei WenbinHamilton EmmaJoy HowardNyangoma StephenWard Douglas GJohnson Philip JIsmail TariqMartin Ashley<p>Abstract</p> <p>Background</p> <p>Colorectal cancer is the second most common cause of cancer related death in the developed world. To date, no blood or stool biomarkers with both high sensitivity and specificity for potentially curable early stage disease have been validated for clinical use. SELDI and MALDI profiling are being used increasingly to search for biomarkers in both blood and urine. Both techniques provide information predominantly on the low molecular weight proteome (<15 kDa). There have been several reports that colorectal cancer is associated with changes in the serum proteome that are detectable by SELDI and we hypothesised that proteomic changes would also be detectable in urine.</p> <p>Results</p> <p>We collected urine from 67 patients with colorectal cancer and 72 non-cancer control subjects, diluted to a constant protein concentration and generated MALDI and SELDI spectra. The intensities of 19 peaks differed significantly between cancer and non-cancer patients by both t-tests and after adjusting for confounders using multiple linear regressions. Logistic regression classifiers based on peak intensities identified colorectal cancer with up to 78% sensitivity at 87% specificity. We identified and independently quantified 3 of the discriminatory peaks using synthetic stable isotope peptides (an 1885 Da fragment of fibrinogen and hepcidin-20) or ELISA (β2-microglobulin).</p> <p>Conclusion</p> <p>Changes in the urine proteome may aid in the early detection of colorectal cancer.</p> http://www.proteomesci.com/content/6/1/19
collection DOAJ
language English
format Article
sources DOAJ
author Wakelam Michael JO
Steven Neil
Tselepis Chris
Wei Wenbin
Hamilton Emma
Joy Howard
Nyangoma Stephen
Ward Douglas G
Johnson Philip J
Ismail Tariq
Martin Ashley
spellingShingle Wakelam Michael JO
Steven Neil
Tselepis Chris
Wei Wenbin
Hamilton Emma
Joy Howard
Nyangoma Stephen
Ward Douglas G
Johnson Philip J
Ismail Tariq
Martin Ashley
Proteomic profiling of urine for the detection of colon cancer
Proteome Science
author_facet Wakelam Michael JO
Steven Neil
Tselepis Chris
Wei Wenbin
Hamilton Emma
Joy Howard
Nyangoma Stephen
Ward Douglas G
Johnson Philip J
Ismail Tariq
Martin Ashley
author_sort Wakelam Michael JO
title Proteomic profiling of urine for the detection of colon cancer
title_short Proteomic profiling of urine for the detection of colon cancer
title_full Proteomic profiling of urine for the detection of colon cancer
title_fullStr Proteomic profiling of urine for the detection of colon cancer
title_full_unstemmed Proteomic profiling of urine for the detection of colon cancer
title_sort proteomic profiling of urine for the detection of colon cancer
publisher BMC
series Proteome Science
issn 1477-5956
publishDate 2008-06-01
description <p>Abstract</p> <p>Background</p> <p>Colorectal cancer is the second most common cause of cancer related death in the developed world. To date, no blood or stool biomarkers with both high sensitivity and specificity for potentially curable early stage disease have been validated for clinical use. SELDI and MALDI profiling are being used increasingly to search for biomarkers in both blood and urine. Both techniques provide information predominantly on the low molecular weight proteome (<15 kDa). There have been several reports that colorectal cancer is associated with changes in the serum proteome that are detectable by SELDI and we hypothesised that proteomic changes would also be detectable in urine.</p> <p>Results</p> <p>We collected urine from 67 patients with colorectal cancer and 72 non-cancer control subjects, diluted to a constant protein concentration and generated MALDI and SELDI spectra. The intensities of 19 peaks differed significantly between cancer and non-cancer patients by both t-tests and after adjusting for confounders using multiple linear regressions. Logistic regression classifiers based on peak intensities identified colorectal cancer with up to 78% sensitivity at 87% specificity. We identified and independently quantified 3 of the discriminatory peaks using synthetic stable isotope peptides (an 1885 Da fragment of fibrinogen and hepcidin-20) or ELISA (β2-microglobulin).</p> <p>Conclusion</p> <p>Changes in the urine proteome may aid in the early detection of colorectal cancer.</p>
url http://www.proteomesci.com/content/6/1/19
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