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A molecular signature for the prediction of recurrence in colorectal cancer

BACKGROUND: Several clinical and pathological factors have an impact on the prognosis of colorectal cancer (CRC), but they are not yet adequate for risk assessment. We aimed to identify a molecular signature that can reliably identify CRC patients at high risk for recurrence. RESULTS: Two hundred ei...

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Autores principales: Wang, Lisha, Shen, Xiaohan, Wang, Zhimin, Xiao, Xiuying, Wei, Ping, Wang, Qifeng, Ren, Fei, Wang, Yiqin, Liu, Zebing, Sheng, Weiqi, Huang, Wei, Zhou, Xiaoyan, Du, Xiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320628/
https://www.ncbi.nlm.nih.gov/pubmed/25645394
http://dx.doi.org/10.1186/s12943-015-0296-2
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author Wang, Lisha
Shen, Xiaohan
Wang, Zhimin
Xiao, Xiuying
Wei, Ping
Wang, Qifeng
Ren, Fei
Wang, Yiqin
Liu, Zebing
Sheng, Weiqi
Huang, Wei
Zhou, Xiaoyan
Du, Xiang
author_facet Wang, Lisha
Shen, Xiaohan
Wang, Zhimin
Xiao, Xiuying
Wei, Ping
Wang, Qifeng
Ren, Fei
Wang, Yiqin
Liu, Zebing
Sheng, Weiqi
Huang, Wei
Zhou, Xiaoyan
Du, Xiang
author_sort Wang, Lisha
collection PubMed
description BACKGROUND: Several clinical and pathological factors have an impact on the prognosis of colorectal cancer (CRC), but they are not yet adequate for risk assessment. We aimed to identify a molecular signature that can reliably identify CRC patients at high risk for recurrence. RESULTS: Two hundred eighty-one CRC samples (stage II/III) were included in this study. A two-step gene expression profiling study was conducted. First, gene expression measurements from 81 fresh frozen CRC samples were obtained using Affymetrix Human Genome U133 Plus 2.0 Arrays. Second, a focused gene expression assay, including prognostic genes and genes of interest from literature reviews, was performed using 200 fresh frozen samples and a Taqman low-density array (TLDA) analysis. An optimal 31-gene expression classifier for the prediction of recurrence among patients with stage II/III CRC was developed using logistic regression analysis. This gene expression signature classified 58.5% of patients as low-risk and 41.5% as high-risk (P < 0.001). The signature was the strongest independent prognostic factor in the multivariate analysis. The five-year relapse-free survival (RFS) rates for the low-risk patients and the high-risk patients were 88.5% and 41.3% (P < 0.001), respectively. CONCLUSION: We identified a 31-gene expression signature that is closely associated with the clinical outcome of stage II/III CRC patients.
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spelling pubmed-43206282015-02-08 A molecular signature for the prediction of recurrence in colorectal cancer Wang, Lisha Shen, Xiaohan Wang, Zhimin Xiao, Xiuying Wei, Ping Wang, Qifeng Ren, Fei Wang, Yiqin Liu, Zebing Sheng, Weiqi Huang, Wei Zhou, Xiaoyan Du, Xiang Mol Cancer Research BACKGROUND: Several clinical and pathological factors have an impact on the prognosis of colorectal cancer (CRC), but they are not yet adequate for risk assessment. We aimed to identify a molecular signature that can reliably identify CRC patients at high risk for recurrence. RESULTS: Two hundred eighty-one CRC samples (stage II/III) were included in this study. A two-step gene expression profiling study was conducted. First, gene expression measurements from 81 fresh frozen CRC samples were obtained using Affymetrix Human Genome U133 Plus 2.0 Arrays. Second, a focused gene expression assay, including prognostic genes and genes of interest from literature reviews, was performed using 200 fresh frozen samples and a Taqman low-density array (TLDA) analysis. An optimal 31-gene expression classifier for the prediction of recurrence among patients with stage II/III CRC was developed using logistic regression analysis. This gene expression signature classified 58.5% of patients as low-risk and 41.5% as high-risk (P < 0.001). The signature was the strongest independent prognostic factor in the multivariate analysis. The five-year relapse-free survival (RFS) rates for the low-risk patients and the high-risk patients were 88.5% and 41.3% (P < 0.001), respectively. CONCLUSION: We identified a 31-gene expression signature that is closely associated with the clinical outcome of stage II/III CRC patients. BioMed Central 2015-02-03 /pmc/articles/PMC4320628/ /pubmed/25645394 http://dx.doi.org/10.1186/s12943-015-0296-2 Text en © Wang et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Lisha
Shen, Xiaohan
Wang, Zhimin
Xiao, Xiuying
Wei, Ping
Wang, Qifeng
Ren, Fei
Wang, Yiqin
Liu, Zebing
Sheng, Weiqi
Huang, Wei
Zhou, Xiaoyan
Du, Xiang
A molecular signature for the prediction of recurrence in colorectal cancer
title A molecular signature for the prediction of recurrence in colorectal cancer
title_full A molecular signature for the prediction of recurrence in colorectal cancer
title_fullStr A molecular signature for the prediction of recurrence in colorectal cancer
title_full_unstemmed A molecular signature for the prediction of recurrence in colorectal cancer
title_short A molecular signature for the prediction of recurrence in colorectal cancer
title_sort molecular signature for the prediction of recurrence in colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320628/
https://www.ncbi.nlm.nih.gov/pubmed/25645394
http://dx.doi.org/10.1186/s12943-015-0296-2
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