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A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer

BACKGROUND: Microsatellite instability (MSI) accounts for about 15% of colorectal cancer and is associated with prognosis. Today, MSI is usually detected by polymerase chain reaction amplification of specific microsatellite markers. However, the instability is identified by comparing the length of m...

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Autores principales: Fu, Yelin, Qi, Lishuang, Guo, Wenbing, Jin, Liangliang, Song, Kai, You, Tianyi, Zhang, Shuobo, Gu, Yunyan, Zhao, Wenyuan, Guo, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813057/
https://www.ncbi.nlm.nih.gov/pubmed/31646964
http://dx.doi.org/10.1186/s12864-019-6129-8
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author Fu, Yelin
Qi, Lishuang
Guo, Wenbing
Jin, Liangliang
Song, Kai
You, Tianyi
Zhang, Shuobo
Gu, Yunyan
Zhao, Wenyuan
Guo, Zheng
author_facet Fu, Yelin
Qi, Lishuang
Guo, Wenbing
Jin, Liangliang
Song, Kai
You, Tianyi
Zhang, Shuobo
Gu, Yunyan
Zhao, Wenyuan
Guo, Zheng
author_sort Fu, Yelin
collection PubMed
description BACKGROUND: Microsatellite instability (MSI) accounts for about 15% of colorectal cancer and is associated with prognosis. Today, MSI is usually detected by polymerase chain reaction amplification of specific microsatellite markers. However, the instability is identified by comparing the length of microsatellite repeats in tumor and normal samples. In this work, we developed a qualitative transcriptional signature to individually predict MSI status for right-sided colon cancer (RCC) based on tumor samples. RESULTS: Using RCC samples, based on the relative expression orderings (REOs) of gene pairs, we extracted a signature consisting of 10 gene pairs (10-GPS) to predict MSI status for RCC through a feature selection process. A sample is predicted as MSI when the gene expression orderings of at least 7 gene pairs vote for MSI; otherwise the microsatellite stability (MSS). The classification performance reached the largest F-score in the training dataset. This signature was verified in four independent datasets of RCCs with the F-scores of 1, 0.9630, 0.9412 and 0.8798, respectively. Additionally, the hierarchical clustering analyses and molecular features also supported the correctness of the reclassifications of the MSI status by 10-GPS. CONCLUSIONS: The qualitative transcriptional signature can be used to classify MSI status of RCC samples at the individualized level.
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spelling pubmed-68130572019-10-30 A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer Fu, Yelin Qi, Lishuang Guo, Wenbing Jin, Liangliang Song, Kai You, Tianyi Zhang, Shuobo Gu, Yunyan Zhao, Wenyuan Guo, Zheng BMC Genomics Research Article BACKGROUND: Microsatellite instability (MSI) accounts for about 15% of colorectal cancer and is associated with prognosis. Today, MSI is usually detected by polymerase chain reaction amplification of specific microsatellite markers. However, the instability is identified by comparing the length of microsatellite repeats in tumor and normal samples. In this work, we developed a qualitative transcriptional signature to individually predict MSI status for right-sided colon cancer (RCC) based on tumor samples. RESULTS: Using RCC samples, based on the relative expression orderings (REOs) of gene pairs, we extracted a signature consisting of 10 gene pairs (10-GPS) to predict MSI status for RCC through a feature selection process. A sample is predicted as MSI when the gene expression orderings of at least 7 gene pairs vote for MSI; otherwise the microsatellite stability (MSS). The classification performance reached the largest F-score in the training dataset. This signature was verified in four independent datasets of RCCs with the F-scores of 1, 0.9630, 0.9412 and 0.8798, respectively. Additionally, the hierarchical clustering analyses and molecular features also supported the correctness of the reclassifications of the MSI status by 10-GPS. CONCLUSIONS: The qualitative transcriptional signature can be used to classify MSI status of RCC samples at the individualized level. BioMed Central 2019-10-23 /pmc/articles/PMC6813057/ /pubmed/31646964 http://dx.doi.org/10.1186/s12864-019-6129-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article
Fu, Yelin
Qi, Lishuang
Guo, Wenbing
Jin, Liangliang
Song, Kai
You, Tianyi
Zhang, Shuobo
Gu, Yunyan
Zhao, Wenyuan
Guo, Zheng
A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer
title A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer
title_full A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer
title_fullStr A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer
title_full_unstemmed A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer
title_short A qualitative transcriptional signature for predicting microsatellite instability status of right-sided Colon Cancer
title_sort qualitative transcriptional signature for predicting microsatellite instability status of right-sided colon cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6813057/
https://www.ncbi.nlm.nih.gov/pubmed/31646964
http://dx.doi.org/10.1186/s12864-019-6129-8
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