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Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer

Pancreatic cancer remains a lethal type of cancer with poor prognosis. Molecular classification enables in-depth, precise prognostic assessment. This study is aimed at identifying a robust and simple mRNA signature to predict the overall survival (OS) of pancreatic cancer (PC) patients. Differential...

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Autores principales: Zhang, Zhiqiang, Gu, Jiangning, Yin, Menghong, Wang, Di, Ma, Chi, Du, Jian, Lin, Zhikun, Hu, Siling, Wang, Xuelong, Li, Ying, Tan, Guang, Luo, Haifeng, Wei, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516738/
https://www.ncbi.nlm.nih.gov/pubmed/33015155
http://dx.doi.org/10.1155/2020/1570862
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author Zhang, Zhiqiang
Gu, Jiangning
Yin, Menghong
Wang, Di
Ma, Chi
Du, Jian
Lin, Zhikun
Hu, Siling
Wang, Xuelong
Li, Ying
Tan, Guang
Luo, Haifeng
Wei, Gang
author_facet Zhang, Zhiqiang
Gu, Jiangning
Yin, Menghong
Wang, Di
Ma, Chi
Du, Jian
Lin, Zhikun
Hu, Siling
Wang, Xuelong
Li, Ying
Tan, Guang
Luo, Haifeng
Wei, Gang
author_sort Zhang, Zhiqiang
collection PubMed
description Pancreatic cancer remains a lethal type of cancer with poor prognosis. Molecular classification enables in-depth, precise prognostic assessment. This study is aimed at identifying a robust and simple mRNA signature to predict the overall survival (OS) of pancreatic cancer (PC) patients. Differentially expressed genes (DEGs) between 45 paired pancreatic tumor samples and adjacent healthy tissues were selected. For risk determination, a LASSO Cox regression model with DEGs was used to generate the OS-associated risk score formula for the training cohort containing 177 PC patients. Another five independent datasets were used as the testing cohort to determine the predictive efficiency for further validation. In total, 441 DEGs were selected after considering the enrichment of classical pathways, such as EMT, cell cycle, cell adhesion, and PI3K-AKT. A five-gene signature for risk discrimination was established with high efficacy using LASSO Cox regression in the training group. External validation showed that patients identified by the gene expression signature to be in the high-risk group had poorer prognosis compared with the low-risk patients. Further investigation identified the differential epigenetic modification patterns of the five genes, which indicated their roles in tumor progression and their effect on therapy. In conclusion, we constructed a robust five-gene expression signature that could predict the OS of PC patients, offering a new insight for risk discrimination in daily clinical practice.
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spelling pubmed-75167382020-10-02 Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer Zhang, Zhiqiang Gu, Jiangning Yin, Menghong Wang, Di Ma, Chi Du, Jian Lin, Zhikun Hu, Siling Wang, Xuelong Li, Ying Tan, Guang Luo, Haifeng Wei, Gang Biomed Res Int Research Article Pancreatic cancer remains a lethal type of cancer with poor prognosis. Molecular classification enables in-depth, precise prognostic assessment. This study is aimed at identifying a robust and simple mRNA signature to predict the overall survival (OS) of pancreatic cancer (PC) patients. Differentially expressed genes (DEGs) between 45 paired pancreatic tumor samples and adjacent healthy tissues were selected. For risk determination, a LASSO Cox regression model with DEGs was used to generate the OS-associated risk score formula for the training cohort containing 177 PC patients. Another five independent datasets were used as the testing cohort to determine the predictive efficiency for further validation. In total, 441 DEGs were selected after considering the enrichment of classical pathways, such as EMT, cell cycle, cell adhesion, and PI3K-AKT. A five-gene signature for risk discrimination was established with high efficacy using LASSO Cox regression in the training group. External validation showed that patients identified by the gene expression signature to be in the high-risk group had poorer prognosis compared with the low-risk patients. Further investigation identified the differential epigenetic modification patterns of the five genes, which indicated their roles in tumor progression and their effect on therapy. In conclusion, we constructed a robust five-gene expression signature that could predict the OS of PC patients, offering a new insight for risk discrimination in daily clinical practice. Hindawi 2020-09-15 /pmc/articles/PMC7516738/ /pubmed/33015155 http://dx.doi.org/10.1155/2020/1570862 Text en Copyright © 2020 Zhiqiang Zhang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Zhiqiang
Gu, Jiangning
Yin, Menghong
Wang, Di
Ma, Chi
Du, Jian
Lin, Zhikun
Hu, Siling
Wang, Xuelong
Li, Ying
Tan, Guang
Luo, Haifeng
Wei, Gang
Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer
title Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer
title_full Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer
title_fullStr Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer
title_full_unstemmed Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer
title_short Establishment and Investigation of a Multiple Gene Expression Signature to Predict Long-Term Survival in Pancreatic Cancer
title_sort establishment and investigation of a multiple gene expression signature to predict long-term survival in pancreatic cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516738/
https://www.ncbi.nlm.nih.gov/pubmed/33015155
http://dx.doi.org/10.1155/2020/1570862
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