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Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening

Methylated SEPT9 showed relatively low sensitivity in detecting early stage colorectal cancer (CRC) and advanced adenomas (AA) in plasma. Combination of multiple biomarkers was an effective strategy to improve sensitivity in early stage cancer diagnosis and screening. A new qPCR‐based assay combinin...

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Autores principales: Zhao, Guodong, Li, Hui, Yang, Zixuan, Wang, Zhenzhen, Xu, Manqiu, Xiong, Shangmin, Li, Shiming, Wu, XiaoTing, Liu, Xiaoyu, Wang, Ziwen, Zhu, Yun, Ma, Yong, Fei, Sujuan, Zheng, Minxue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745865/
https://www.ncbi.nlm.nih.gov/pubmed/31407497
http://dx.doi.org/10.1002/cam4.2475
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author Zhao, Guodong
Li, Hui
Yang, Zixuan
Wang, Zhenzhen
Xu, Manqiu
Xiong, Shangmin
Li, Shiming
Wu, XiaoTing
Liu, Xiaoyu
Wang, Ziwen
Zhu, Yun
Ma, Yong
Fei, Sujuan
Zheng, Minxue
author_facet Zhao, Guodong
Li, Hui
Yang, Zixuan
Wang, Zhenzhen
Xu, Manqiu
Xiong, Shangmin
Li, Shiming
Wu, XiaoTing
Liu, Xiaoyu
Wang, Ziwen
Zhu, Yun
Ma, Yong
Fei, Sujuan
Zheng, Minxue
author_sort Zhao, Guodong
collection PubMed
description Methylated SEPT9 showed relatively low sensitivity in detecting early stage colorectal cancer (CRC) and advanced adenomas (AA) in plasma. Combination of multiple biomarkers was an effective strategy to improve sensitivity in early stage cancer diagnosis and screening. A new qPCR‐based assay combining the detection of methylated SEPT9 and SDC2 (ColoDefense test) was used. Methylation statuses of SEPT9 and SDC2 were examined in 40 sets of cancer tissues and paired adjacent tissues, 10 adenomatous polyps and 3 hyperplastic polyps (HP). Then evaluated with 384 plasma samples, including 117 CRC patients, 23 AA patients, 78 small polyps patients, and 166 normal individuals. The limit of detection of ColoDefense was about 25 pg per reaction. Both SEPT9 and SDC2 were shown by ColoDefense to be heavily methylated in CRC tissues when compared to paired paracancerous tissues and HP (P < .01). The sensitivities for detecting AA and stage I CRC by plasma SEPT9 methylation alone were 12.1% and 65.0%, and those by plasma SDC2 methylation alone were 43.5% and 55.0%. In comparison, the sensitivities to detect AA and stage I CRC by ColoDefense improved to 47.8% and 80.0%. The overall sensitivity of ColoDefense in detecting CRC was 88.9% (95% CI: 81.4%‐93.7%) with a specificity of 92.8% (95% CI: 87.4%‐96.0%). Detection of the combinatorial biomarker of methylated SEPT9 and/or SDC2 is a powerful, convenient and highly effective strategy for early CRC screening with high sensitivity and specificity.
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spelling pubmed-67458652019-09-18 Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening Zhao, Guodong Li, Hui Yang, Zixuan Wang, Zhenzhen Xu, Manqiu Xiong, Shangmin Li, Shiming Wu, XiaoTing Liu, Xiaoyu Wang, Ziwen Zhu, Yun Ma, Yong Fei, Sujuan Zheng, Minxue Cancer Med Clinical Cancer Research Methylated SEPT9 showed relatively low sensitivity in detecting early stage colorectal cancer (CRC) and advanced adenomas (AA) in plasma. Combination of multiple biomarkers was an effective strategy to improve sensitivity in early stage cancer diagnosis and screening. A new qPCR‐based assay combining the detection of methylated SEPT9 and SDC2 (ColoDefense test) was used. Methylation statuses of SEPT9 and SDC2 were examined in 40 sets of cancer tissues and paired adjacent tissues, 10 adenomatous polyps and 3 hyperplastic polyps (HP). Then evaluated with 384 plasma samples, including 117 CRC patients, 23 AA patients, 78 small polyps patients, and 166 normal individuals. The limit of detection of ColoDefense was about 25 pg per reaction. Both SEPT9 and SDC2 were shown by ColoDefense to be heavily methylated in CRC tissues when compared to paired paracancerous tissues and HP (P < .01). The sensitivities for detecting AA and stage I CRC by plasma SEPT9 methylation alone were 12.1% and 65.0%, and those by plasma SDC2 methylation alone were 43.5% and 55.0%. In comparison, the sensitivities to detect AA and stage I CRC by ColoDefense improved to 47.8% and 80.0%. The overall sensitivity of ColoDefense in detecting CRC was 88.9% (95% CI: 81.4%‐93.7%) with a specificity of 92.8% (95% CI: 87.4%‐96.0%). Detection of the combinatorial biomarker of methylated SEPT9 and/or SDC2 is a powerful, convenient and highly effective strategy for early CRC screening with high sensitivity and specificity. John Wiley and Sons Inc. 2019-08-12 /pmc/articles/PMC6745865/ /pubmed/31407497 http://dx.doi.org/10.1002/cam4.2475 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Zhao, Guodong
Li, Hui
Yang, Zixuan
Wang, Zhenzhen
Xu, Manqiu
Xiong, Shangmin
Li, Shiming
Wu, XiaoTing
Liu, Xiaoyu
Wang, Ziwen
Zhu, Yun
Ma, Yong
Fei, Sujuan
Zheng, Minxue
Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening
title Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening
title_full Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening
title_fullStr Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening
title_full_unstemmed Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening
title_short Multiplex methylated DNA testing in plasma with high sensitivity and specificity for colorectal cancer screening
title_sort multiplex methylated dna testing in plasma with high sensitivity and specificity for colorectal cancer screening
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6745865/
https://www.ncbi.nlm.nih.gov/pubmed/31407497
http://dx.doi.org/10.1002/cam4.2475
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