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Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy

We aimed to identify prognostic signature based on autophagy-related genes (ARGs) for breast cancer patients. The datasets of breast cancer were downloaded from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO). Least absolute shrinkage and selection operator (LASSO) Cox regression wa...

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Autores principales: Zhong, Shanliang, Chen, Huanwen, Yang, Sujin, Feng, Jifeng, Zhou, Siying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391974/
https://www.ncbi.nlm.nih.gov/pubmed/33194339
http://dx.doi.org/10.7717/peerj.9621
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author Zhong, Shanliang
Chen, Huanwen
Yang, Sujin
Feng, Jifeng
Zhou, Siying
author_facet Zhong, Shanliang
Chen, Huanwen
Yang, Sujin
Feng, Jifeng
Zhou, Siying
author_sort Zhong, Shanliang
collection PubMed
description We aimed to identify prognostic signature based on autophagy-related genes (ARGs) for breast cancer patients. The datasets of breast cancer were downloaded from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO). Least absolute shrinkage and selection operator (LASSO) Cox regression was conducted to construct multiple-ARG risk signature. In total, 32 ARGs were identified as differentially expressed between tumors and adjacent normal tissues based on TCGA. Six ARGs (IFNG, TP63, PPP1R15A, PTK6, EIF4EBP1 and NKX2-3) with non-zero coefficient were selected from the 32 ARGs using LASSO regression. The 6-ARG signature divided patients into high-and low-risk group. Survival analysis indicated that low-risk group had longer survival time than high-risk group. We further validated the 6-ARG signature using dataset from GEO and found similar results. We analyzed the associations between ARGs and breast cancer survival in TCGA and nine GEO datasets, and obtained 170 ARGs with significant associations. EIF4EBP1, FOS and FAS were the top three ARGs with highest numbers of significant associations. EIF4EBP1 may be a key ARG which had a higher expression level in patients with more malignant molecular subtypes and higher grade breast cancer. In conclusion, our 6-ARG signature was of significance in predicting of overall survival of patients with breast cancer. EIF4EBP1 may be a key ARG associated with breast cancer survival.
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spelling pubmed-73919742020-11-12 Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy Zhong, Shanliang Chen, Huanwen Yang, Sujin Feng, Jifeng Zhou, Siying PeerJ Bioinformatics We aimed to identify prognostic signature based on autophagy-related genes (ARGs) for breast cancer patients. The datasets of breast cancer were downloaded from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO). Least absolute shrinkage and selection operator (LASSO) Cox regression was conducted to construct multiple-ARG risk signature. In total, 32 ARGs were identified as differentially expressed between tumors and adjacent normal tissues based on TCGA. Six ARGs (IFNG, TP63, PPP1R15A, PTK6, EIF4EBP1 and NKX2-3) with non-zero coefficient were selected from the 32 ARGs using LASSO regression. The 6-ARG signature divided patients into high-and low-risk group. Survival analysis indicated that low-risk group had longer survival time than high-risk group. We further validated the 6-ARG signature using dataset from GEO and found similar results. We analyzed the associations between ARGs and breast cancer survival in TCGA and nine GEO datasets, and obtained 170 ARGs with significant associations. EIF4EBP1, FOS and FAS were the top three ARGs with highest numbers of significant associations. EIF4EBP1 may be a key ARG which had a higher expression level in patients with more malignant molecular subtypes and higher grade breast cancer. In conclusion, our 6-ARG signature was of significance in predicting of overall survival of patients with breast cancer. EIF4EBP1 may be a key ARG associated with breast cancer survival. PeerJ Inc. 2020-07-27 /pmc/articles/PMC7391974/ /pubmed/33194339 http://dx.doi.org/10.7717/peerj.9621 Text en © 2020 Zhong et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Bioinformatics
Zhong, Shanliang
Chen, Huanwen
Yang, Sujin
Feng, Jifeng
Zhou, Siying
Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy
title Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy
title_full Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy
title_fullStr Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy
title_full_unstemmed Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy
title_short Identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy
title_sort identification and validation of prognostic signature for breast cancer based on genes potentially involved in autophagy
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391974/
https://www.ncbi.nlm.nih.gov/pubmed/33194339
http://dx.doi.org/10.7717/peerj.9621
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