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A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA
BACKGROUND: ColoDefense1.0 assay has demonstrated its excellent sensitivity and specificity for early detection of colorectal cancer (CRC) by detecting the methylation levels of SDC2 and SEPT9, while exhibited limitations on relatively large sample capacity required and limited detection throughput...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540293/ https://www.ncbi.nlm.nih.gov/pubmed/36203138 http://dx.doi.org/10.1186/s12876-022-02512-6 |
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author | Dai, Yanmiao Zhao, Guodong Yang, Jun Zhou, Xilang Xiong, Shangmin Lu, Xirong Gao, Liming Wu, Jianfang Xu, Zouhua Fei, Sujuan Zheng, Minxue Xu, Hongwei |
author_facet | Dai, Yanmiao Zhao, Guodong Yang, Jun Zhou, Xilang Xiong, Shangmin Lu, Xirong Gao, Liming Wu, Jianfang Xu, Zouhua Fei, Sujuan Zheng, Minxue Xu, Hongwei |
author_sort | Dai, Yanmiao |
collection | PubMed |
description | BACKGROUND: ColoDefense1.0 assay has demonstrated its excellent sensitivity and specificity for early detection of colorectal cancer (CRC) by detecting the methylation levels of SDC2 and SEPT9, while exhibited limitations on relatively large sample capacity required and limited detection throughput by applying triplicate PCR reactions for each sample. In this study, ColoDefense1.0 was simplified and optimized into ColoDefense2.0 in a single PCR reaction. METHODS: A total 529 stool specimens were collected, and 244 CRC patients, 34 patients with advanced adenomas (AA), 64 with small polyps (SP) and 187 control subjects were divided in training and validation cohorts. Methylation levels of SEPT9 and SDC2 were examined by qPCR reactions in triplicate or single. RESULTS: The stool DNA quantity stored in preservative buffer at 37 °C up to 7 days exhibited no significant decrease. In the training cohort, when the number of replicates reduced from 3 to 1, the overall performance of ColoDefense2.0 was identical to that of ColoDefense1.0, showing sensitivities of 71.4% for AA and 90.8% for all stage CRC with a specificity of 92.9%. In the validation cohort, sensitivities of SP, AA and CRC using ColoDefense2.0 were 25.0%, 55.0% and 88.2%, increased from 14.1% (20.3%), 40.0% (40.0%) and 79.4% (67.6%) using SDC2 (SEPT9) alone; along with an overall specificity of 90.2%, decreased from 94.1% (95.1%) using SDC2 (SEPT9) alone. CONCLUSION: The simplified ColoDefense test maintained the overall performance while reduced the number of PCR reactions to 1/3, and provided an effective and convenient tool to detect early CRC and precancerous lesions and potentially improve the compliance of screening. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02512-6. |
format | Online Article Text |
id | pubmed-9540293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95402932022-10-08 A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA Dai, Yanmiao Zhao, Guodong Yang, Jun Zhou, Xilang Xiong, Shangmin Lu, Xirong Gao, Liming Wu, Jianfang Xu, Zouhua Fei, Sujuan Zheng, Minxue Xu, Hongwei BMC Gastroenterol Research BACKGROUND: ColoDefense1.0 assay has demonstrated its excellent sensitivity and specificity for early detection of colorectal cancer (CRC) by detecting the methylation levels of SDC2 and SEPT9, while exhibited limitations on relatively large sample capacity required and limited detection throughput by applying triplicate PCR reactions for each sample. In this study, ColoDefense1.0 was simplified and optimized into ColoDefense2.0 in a single PCR reaction. METHODS: A total 529 stool specimens were collected, and 244 CRC patients, 34 patients with advanced adenomas (AA), 64 with small polyps (SP) and 187 control subjects were divided in training and validation cohorts. Methylation levels of SEPT9 and SDC2 were examined by qPCR reactions in triplicate or single. RESULTS: The stool DNA quantity stored in preservative buffer at 37 °C up to 7 days exhibited no significant decrease. In the training cohort, when the number of replicates reduced from 3 to 1, the overall performance of ColoDefense2.0 was identical to that of ColoDefense1.0, showing sensitivities of 71.4% for AA and 90.8% for all stage CRC with a specificity of 92.9%. In the validation cohort, sensitivities of SP, AA and CRC using ColoDefense2.0 were 25.0%, 55.0% and 88.2%, increased from 14.1% (20.3%), 40.0% (40.0%) and 79.4% (67.6%) using SDC2 (SEPT9) alone; along with an overall specificity of 90.2%, decreased from 94.1% (95.1%) using SDC2 (SEPT9) alone. CONCLUSION: The simplified ColoDefense test maintained the overall performance while reduced the number of PCR reactions to 1/3, and provided an effective and convenient tool to detect early CRC and precancerous lesions and potentially improve the compliance of screening. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02512-6. BioMed Central 2022-10-06 /pmc/articles/PMC9540293/ /pubmed/36203138 http://dx.doi.org/10.1186/s12876-022-02512-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Dai, Yanmiao Zhao, Guodong Yang, Jun Zhou, Xilang Xiong, Shangmin Lu, Xirong Gao, Liming Wu, Jianfang Xu, Zouhua Fei, Sujuan Zheng, Minxue Xu, Hongwei A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA |
title | A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA |
title_full | A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA |
title_fullStr | A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA |
title_full_unstemmed | A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA |
title_short | A simplified multiplex methylated DNA testing for early detection of colorectal cancer in stool DNA |
title_sort | simplified multiplex methylated dna testing for early detection of colorectal cancer in stool dna |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540293/ https://www.ncbi.nlm.nih.gov/pubmed/36203138 http://dx.doi.org/10.1186/s12876-022-02512-6 |
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