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Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer

BACKGROUND: Breast cancer (BC) is an aging‐related disease. Aging‐related genes (ARGs) participate in the initiation and development of lung and colon cancer, but the prognosis signature of ARGs in BC has not been clearly studied. AIMS: This study aimed to construct an ARGs signature to predict the...

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Autores principales: Li, Jian, Qi, Chunling, Li, Qing, Liu, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026283/
https://www.ncbi.nlm.nih.gov/pubmed/36323529
http://dx.doi.org/10.1002/cnr2.1741
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author Li, Jian
Qi, Chunling
Li, Qing
Liu, Fei
author_facet Li, Jian
Qi, Chunling
Li, Qing
Liu, Fei
author_sort Li, Jian
collection PubMed
description BACKGROUND: Breast cancer (BC) is an aging‐related disease. Aging‐related genes (ARGs) participate in the initiation and development of lung and colon cancer, but the prognosis signature of ARGs in BC has not been clearly studied. AIMS: This study aimed to construct an ARGs signature to predict the prognosis of patients with breast cancer. METHOD: Firstly, the expression data of ARGs from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) were collected. Then COX and least absolulute shrinkage and selection operator(LASSO) were performed to construct the ARGs prognostic signature. The correlation between the signature and immune cell infiltration, immunotherapeutic response and drug sensitivity were subsequently analysed. The TCGA nomogram was constructed by combining the signature with other clinical features, and was validated by using GEO database. RESULTS: After LASSO and COX regression analyses, a prognostic signature based on nine ARGs, namely, HSP90AA1, NFKB2, PLAU, PTK2, RECQL4, CLU, JAK2, MAP3K5, and S100B, was built by using the TCGA dataset. Moreover, this risk signature is closely related to immune cell infiltration, immunotherapeutic response, and responses to chemotherapy and targeted therapy. Subsequently, The calibration curve demonstrates that the nomogram agrees well with practical prediction results. The receiver operating characteristic curve and decision‐making curve analysis demonstrate that ARG signature has the better prognosis diagnosis ability and clinical net benefits. CONCLUSIONS: Therefore, the proposed ARG prognosis signature is a new prognosis molecular marker of patients with BC, and it can provide good references to individual clinical therapy.
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spelling pubmed-100262832023-03-21 Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer Li, Jian Qi, Chunling Li, Qing Liu, Fei Cancer Rep (Hoboken) Original Articles BACKGROUND: Breast cancer (BC) is an aging‐related disease. Aging‐related genes (ARGs) participate in the initiation and development of lung and colon cancer, but the prognosis signature of ARGs in BC has not been clearly studied. AIMS: This study aimed to construct an ARGs signature to predict the prognosis of patients with breast cancer. METHOD: Firstly, the expression data of ARGs from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) were collected. Then COX and least absolulute shrinkage and selection operator(LASSO) were performed to construct the ARGs prognostic signature. The correlation between the signature and immune cell infiltration, immunotherapeutic response and drug sensitivity were subsequently analysed. The TCGA nomogram was constructed by combining the signature with other clinical features, and was validated by using GEO database. RESULTS: After LASSO and COX regression analyses, a prognostic signature based on nine ARGs, namely, HSP90AA1, NFKB2, PLAU, PTK2, RECQL4, CLU, JAK2, MAP3K5, and S100B, was built by using the TCGA dataset. Moreover, this risk signature is closely related to immune cell infiltration, immunotherapeutic response, and responses to chemotherapy and targeted therapy. Subsequently, The calibration curve demonstrates that the nomogram agrees well with practical prediction results. The receiver operating characteristic curve and decision‐making curve analysis demonstrate that ARG signature has the better prognosis diagnosis ability and clinical net benefits. CONCLUSIONS: Therefore, the proposed ARG prognosis signature is a new prognosis molecular marker of patients with BC, and it can provide good references to individual clinical therapy. John Wiley and Sons Inc. 2022-11-02 /pmc/articles/PMC10026283/ /pubmed/36323529 http://dx.doi.org/10.1002/cnr2.1741 Text en © 2022 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Li, Jian
Qi, Chunling
Li, Qing
Liu, Fei
Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer
title Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer
title_full Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer
title_fullStr Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer
title_full_unstemmed Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer
title_short Construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer
title_sort construction and validation of an aging‐related gene signature for prognosis prediction of patients with breast cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026283/
https://www.ncbi.nlm.nih.gov/pubmed/36323529
http://dx.doi.org/10.1002/cnr2.1741
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