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Identification of long-term survival-associated gene in breast cancer

Breast cancer patients at the same stage may show different clinical prognoses or different therapeutic effects of systemic therapy. Differentially expressed genes of breast cancer were identified from GSE42568. Through survival, receiver operating characteristic (ROC) curve, random forest, GSVA and...

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Autores principales: Ning, Shipeng, Li, Hui, Qiao, Kun, Wang, Qin, Shen, Meiying, Kang, Yujuan, Yin, Yanling, Liu, Jiena, Liu, Lei, Hou, Siyu, Wang, Jianyu, Xu, Shouping, Pang, Da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655188/
https://www.ncbi.nlm.nih.gov/pubmed/33080569
http://dx.doi.org/10.18632/aging.103807
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author Ning, Shipeng
Li, Hui
Qiao, Kun
Wang, Qin
Shen, Meiying
Kang, Yujuan
Yin, Yanling
Liu, Jiena
Liu, Lei
Hou, Siyu
Wang, Jianyu
Xu, Shouping
Pang, Da
author_facet Ning, Shipeng
Li, Hui
Qiao, Kun
Wang, Qin
Shen, Meiying
Kang, Yujuan
Yin, Yanling
Liu, Jiena
Liu, Lei
Hou, Siyu
Wang, Jianyu
Xu, Shouping
Pang, Da
author_sort Ning, Shipeng
collection PubMed
description Breast cancer patients at the same stage may show different clinical prognoses or different therapeutic effects of systemic therapy. Differentially expressed genes of breast cancer were identified from GSE42568. Through survival, receiver operating characteristic (ROC) curve, random forest, GSVA and a Cox regression model analyses, genes were identified that could be associated with survival time in breast cancer. The molecular mechanism was identified by enrichment, GSEA, methylation and SNV analyses. Then, the expression of a key gene was verified by the TCGA dataset and RT-qPCR, Western blot, and immunohistochemistry. We identified 784 genes related to the 5-year overall survival time of breast cancer. Through ROC curve and random forest analysis, 10 prognostic genes were screened. These were integrated into a complex by GSVA, and high expression of the complex significantly promoted the recurrence-free survival of patients. In addition, key genes were related to immune and metabolic-related functions. Importantly, we identified methylation of MEX3A and TBC1D 9 and mutations events. Finally, the expression of UGCG was verified by the TCGA dataset and by experimental methods in our own samples. These results indicate that 10 genes may be potential biomarkers and therapeutic targets for long-term survival in breast cancer, especially UGCG.
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spelling pubmed-76551882020-11-19 Identification of long-term survival-associated gene in breast cancer Ning, Shipeng Li, Hui Qiao, Kun Wang, Qin Shen, Meiying Kang, Yujuan Yin, Yanling Liu, Jiena Liu, Lei Hou, Siyu Wang, Jianyu Xu, Shouping Pang, Da Aging (Albany NY) Research Paper Breast cancer patients at the same stage may show different clinical prognoses or different therapeutic effects of systemic therapy. Differentially expressed genes of breast cancer were identified from GSE42568. Through survival, receiver operating characteristic (ROC) curve, random forest, GSVA and a Cox regression model analyses, genes were identified that could be associated with survival time in breast cancer. The molecular mechanism was identified by enrichment, GSEA, methylation and SNV analyses. Then, the expression of a key gene was verified by the TCGA dataset and RT-qPCR, Western blot, and immunohistochemistry. We identified 784 genes related to the 5-year overall survival time of breast cancer. Through ROC curve and random forest analysis, 10 prognostic genes were screened. These were integrated into a complex by GSVA, and high expression of the complex significantly promoted the recurrence-free survival of patients. In addition, key genes were related to immune and metabolic-related functions. Importantly, we identified methylation of MEX3A and TBC1D 9 and mutations events. Finally, the expression of UGCG was verified by the TCGA dataset and by experimental methods in our own samples. These results indicate that 10 genes may be potential biomarkers and therapeutic targets for long-term survival in breast cancer, especially UGCG. Impact Journals 2020-10-20 /pmc/articles/PMC7655188/ /pubmed/33080569 http://dx.doi.org/10.18632/aging.103807 Text en Copyright: © 2020 Ning et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ning, Shipeng
Li, Hui
Qiao, Kun
Wang, Qin
Shen, Meiying
Kang, Yujuan
Yin, Yanling
Liu, Jiena
Liu, Lei
Hou, Siyu
Wang, Jianyu
Xu, Shouping
Pang, Da
Identification of long-term survival-associated gene in breast cancer
title Identification of long-term survival-associated gene in breast cancer
title_full Identification of long-term survival-associated gene in breast cancer
title_fullStr Identification of long-term survival-associated gene in breast cancer
title_full_unstemmed Identification of long-term survival-associated gene in breast cancer
title_short Identification of long-term survival-associated gene in breast cancer
title_sort identification of long-term survival-associated gene in breast cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7655188/
https://www.ncbi.nlm.nih.gov/pubmed/33080569
http://dx.doi.org/10.18632/aging.103807
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