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A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer

BACKGROUND: Specific genes are methylated with high frequency in colorectal neoplasia, and may leak into blood. Detection of multiple methylated DNA biomarkers in blood may improve assay sensitivity for colorectal cancer (CRC) relative to a single marker. We undertook a case-control study evaluating...

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Autores principales: Pedersen, Susanne K., Baker, Rohan T., McEvoy, Aidan, Murray, David H., Thomas, Melissa, Molloy, Peter L., Mitchell, Sue, Lockett, Trevor, Young, Graeme P., LaPointe, Lawrence C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416022/
https://www.ncbi.nlm.nih.gov/pubmed/25928810
http://dx.doi.org/10.1371/journal.pone.0125041
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author Pedersen, Susanne K.
Baker, Rohan T.
McEvoy, Aidan
Murray, David H.
Thomas, Melissa
Molloy, Peter L.
Mitchell, Sue
Lockett, Trevor
Young, Graeme P.
LaPointe, Lawrence C.
author_facet Pedersen, Susanne K.
Baker, Rohan T.
McEvoy, Aidan
Murray, David H.
Thomas, Melissa
Molloy, Peter L.
Mitchell, Sue
Lockett, Trevor
Young, Graeme P.
LaPointe, Lawrence C.
author_sort Pedersen, Susanne K.
collection PubMed
description BACKGROUND: Specific genes are methylated with high frequency in colorectal neoplasia, and may leak into blood. Detection of multiple methylated DNA biomarkers in blood may improve assay sensitivity for colorectal cancer (CRC) relative to a single marker. We undertook a case-control study evaluating the presence of two methylation DNA markers, BCAT1 and IKZF1, in circulation to determine if they were complementary for detection of CRC. METHODS: Methylation-specific PCR assays were developed to measure the level of methylated BCAT1 and IKZF1 in DNA extracted from plasma obtained from colonoscopy-confirmed 144 healthy controls and 74 CRC cases. RESULTS: DNA yields ranged from 2 to 730 ng/mL plasma (mean 18.6ng/mL; 95% CI 11-26 ng/mL) and did not correlate with gender, age or CRC status. Methylated BCAT1 and IKZF1 DNA were detected in respectively 48 (65%) and 50 (68%) of the 74 cancers. In contrast, only 5 (4%) and 7 (5%) controls were positive for BCAT1 and IKZF1 DNA methylation, respectively. A two-gene classifier model (“either or” rule) improved segregation of CRC from controls, with 57 of 74 cancers (77%) compared to only 11 of 144 (7.6%) controls being positive for BCAT1 and/or IKZF1 DNA methylation. Increasing levels of methylated DNA were observed as CRC stage progressed. CONCLUSIONS: Detection of methylated BCAT1 and/or IKZF1 DNA in plasma may have clinical application as a novel blood test for CRC. Combining the results from the two methylation-specific PCR assays improved CRC detection with minimal change in specificity. Further validation of this two-gene blood test with a view to application in screening is now indicated.
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spelling pubmed-44160222015-05-07 A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer Pedersen, Susanne K. Baker, Rohan T. McEvoy, Aidan Murray, David H. Thomas, Melissa Molloy, Peter L. Mitchell, Sue Lockett, Trevor Young, Graeme P. LaPointe, Lawrence C. PLoS One Research Article BACKGROUND: Specific genes are methylated with high frequency in colorectal neoplasia, and may leak into blood. Detection of multiple methylated DNA biomarkers in blood may improve assay sensitivity for colorectal cancer (CRC) relative to a single marker. We undertook a case-control study evaluating the presence of two methylation DNA markers, BCAT1 and IKZF1, in circulation to determine if they were complementary for detection of CRC. METHODS: Methylation-specific PCR assays were developed to measure the level of methylated BCAT1 and IKZF1 in DNA extracted from plasma obtained from colonoscopy-confirmed 144 healthy controls and 74 CRC cases. RESULTS: DNA yields ranged from 2 to 730 ng/mL plasma (mean 18.6ng/mL; 95% CI 11-26 ng/mL) and did not correlate with gender, age or CRC status. Methylated BCAT1 and IKZF1 DNA were detected in respectively 48 (65%) and 50 (68%) of the 74 cancers. In contrast, only 5 (4%) and 7 (5%) controls were positive for BCAT1 and IKZF1 DNA methylation, respectively. A two-gene classifier model (“either or” rule) improved segregation of CRC from controls, with 57 of 74 cancers (77%) compared to only 11 of 144 (7.6%) controls being positive for BCAT1 and/or IKZF1 DNA methylation. Increasing levels of methylated DNA were observed as CRC stage progressed. CONCLUSIONS: Detection of methylated BCAT1 and/or IKZF1 DNA in plasma may have clinical application as a novel blood test for CRC. Combining the results from the two methylation-specific PCR assays improved CRC detection with minimal change in specificity. Further validation of this two-gene blood test with a view to application in screening is now indicated. Public Library of Science 2015-04-30 /pmc/articles/PMC4416022/ /pubmed/25928810 http://dx.doi.org/10.1371/journal.pone.0125041 Text en © 2015 Pedersen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pedersen, Susanne K.
Baker, Rohan T.
McEvoy, Aidan
Murray, David H.
Thomas, Melissa
Molloy, Peter L.
Mitchell, Sue
Lockett, Trevor
Young, Graeme P.
LaPointe, Lawrence C.
A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer
title A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer
title_full A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer
title_fullStr A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer
title_full_unstemmed A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer
title_short A Two-Gene Blood Test for Methylated DNA Sensitive for Colorectal Cancer
title_sort two-gene blood test for methylated dna sensitive for colorectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4416022/
https://www.ncbi.nlm.nih.gov/pubmed/25928810
http://dx.doi.org/10.1371/journal.pone.0125041
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