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Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures

Detection of methylation patterns in circulating tumor DNA (ctDNA) can offer a novel approach for cancer diagnostics given the unique signature for each tumor type. We developed a next-generation sequencing (NGS)-based assay targeting 32 CpG sites to detect colorectal cancer-specific ctDNA. NGS was...

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Autores principales: Gouda, Mohamed A, Duose, Dzifa Y, Lapin, Morten, Zalles, Stephanie, Huang, Helen J, Xi, Yuanxin, Zheng, Xiaofeng, Aldesoky, Amira I, Alhanafy, Alshimaa M, Shehata, Mohamed A, Wang, Jing, Kopetz, Scott, Meric-Bernstam, Funda, Wistuba, Ignacio I, Luthra, Rajyalakshmi, Janku, Filip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078907/
https://www.ncbi.nlm.nih.gov/pubmed/36200910
http://dx.doi.org/10.1093/oncolo/oyac204
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author Gouda, Mohamed A
Duose, Dzifa Y
Lapin, Morten
Zalles, Stephanie
Huang, Helen J
Xi, Yuanxin
Zheng, Xiaofeng
Aldesoky, Amira I
Alhanafy, Alshimaa M
Shehata, Mohamed A
Wang, Jing
Kopetz, Scott
Meric-Bernstam, Funda
Wistuba, Ignacio I
Luthra, Rajyalakshmi
Janku, Filip
author_facet Gouda, Mohamed A
Duose, Dzifa Y
Lapin, Morten
Zalles, Stephanie
Huang, Helen J
Xi, Yuanxin
Zheng, Xiaofeng
Aldesoky, Amira I
Alhanafy, Alshimaa M
Shehata, Mohamed A
Wang, Jing
Kopetz, Scott
Meric-Bernstam, Funda
Wistuba, Ignacio I
Luthra, Rajyalakshmi
Janku, Filip
author_sort Gouda, Mohamed A
collection PubMed
description Detection of methylation patterns in circulating tumor DNA (ctDNA) can offer a novel approach for cancer diagnostics given the unique signature for each tumor type. We developed a next-generation sequencing (NGS)-based assay targeting 32 CpG sites to detect colorectal cancer-specific ctDNA. NGS was performed on bisulfite-converted libraries and status dichotomization was done using median methylation ratios at all targets. We included plasma samples from patients with metastatic colorectal (n = 20) and non-colorectal cancers (n = 8); and healthy volunteers (n = 4). Median methylation ratio was higher in colorectal cancer compared with non-colorectal cancers (P = .001) and normal donors (P = .005). The assay detected ctDNA in 85% of patients with colorectal cancer at a specificity of 92%. Notably, we were able to detect methylated ctDNA in 75% of patients in whom ctDNA was not detected by other methods. Detection of methylated ctDNA was associated with shorter median progression-free survival compared to non-detection (8 weeks versus 54 weeks; P = .027).
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spelling pubmed-100789072023-04-07 Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures Gouda, Mohamed A Duose, Dzifa Y Lapin, Morten Zalles, Stephanie Huang, Helen J Xi, Yuanxin Zheng, Xiaofeng Aldesoky, Amira I Alhanafy, Alshimaa M Shehata, Mohamed A Wang, Jing Kopetz, Scott Meric-Bernstam, Funda Wistuba, Ignacio I Luthra, Rajyalakshmi Janku, Filip Oncologist Brief Communications Detection of methylation patterns in circulating tumor DNA (ctDNA) can offer a novel approach for cancer diagnostics given the unique signature for each tumor type. We developed a next-generation sequencing (NGS)-based assay targeting 32 CpG sites to detect colorectal cancer-specific ctDNA. NGS was performed on bisulfite-converted libraries and status dichotomization was done using median methylation ratios at all targets. We included plasma samples from patients with metastatic colorectal (n = 20) and non-colorectal cancers (n = 8); and healthy volunteers (n = 4). Median methylation ratio was higher in colorectal cancer compared with non-colorectal cancers (P = .001) and normal donors (P = .005). The assay detected ctDNA in 85% of patients with colorectal cancer at a specificity of 92%. Notably, we were able to detect methylated ctDNA in 75% of patients in whom ctDNA was not detected by other methods. Detection of methylated ctDNA was associated with shorter median progression-free survival compared to non-detection (8 weeks versus 54 weeks; P = .027). Oxford University Press 2022-10-06 /pmc/articles/PMC10078907/ /pubmed/36200910 http://dx.doi.org/10.1093/oncolo/oyac204 Text en © The Author(s) 2022. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.
spellingShingle Brief Communications
Gouda, Mohamed A
Duose, Dzifa Y
Lapin, Morten
Zalles, Stephanie
Huang, Helen J
Xi, Yuanxin
Zheng, Xiaofeng
Aldesoky, Amira I
Alhanafy, Alshimaa M
Shehata, Mohamed A
Wang, Jing
Kopetz, Scott
Meric-Bernstam, Funda
Wistuba, Ignacio I
Luthra, Rajyalakshmi
Janku, Filip
Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures
title Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures
title_full Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures
title_fullStr Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures
title_full_unstemmed Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures
title_short Mutation-Agnostic Detection of Colorectal Cancer Using Liquid Biopsy-Based Methylation-Specific Signatures
title_sort mutation-agnostic detection of colorectal cancer using liquid biopsy-based methylation-specific signatures
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078907/
https://www.ncbi.nlm.nih.gov/pubmed/36200910
http://dx.doi.org/10.1093/oncolo/oyac204
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