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pmid:33080569

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

Shipeng Ning · Hui Li · Kun Qiao · Qin Wang · Meiying Shen · Yujuan Kang · Yanling Yin · Jiena Liu · Lei Liu · Siyu Hou · Jianyu Wang · Shouping Xu · Da Pang

Aging · 2020 doi:10.18632/aging.103807

Paper

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Experiment

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Data

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Analysis

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pmid:33080569
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title
Identification of long-term survival-associated gene in breast cancer.
doi
10.18632/aging.103807
pmid
33080569
authors array · 13 items
[0]
Shipeng Ning
[1]
Hui Li
[2]
Kun Qiao
[3]
Qin Wang
[4]
Meiying Shen
[5]
Yujuan Kang
[6]
Yanling Yin
[7]
Jiena Liu
[8]
Lei Liu
[9]
Siyu Hou
[10]
Jianyu Wang
[11]
Shouping Xu
[12]
Da Pang
journal
Aging
year
2020
abstract
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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A single factor Cox regression model was used to calculate the influence of clinical characteristics and mRNA expression level on the prognosis of breast cancer patients.
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A single factor Cox regression model was used to calculate the influence of clinical characteristics and mRNA expression level on the prognosis of breast cancer patients.
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title
Strong Time Dependence of the 76-Gene Prognostic Signature
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Quantitative real-time PCR with reverse transcription (qRT–PCR)
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The paper names GSE42568, GSE37751, GSE7390, GSE37754 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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A single factor Cox regression model was used to calculate the influence of clinical characteristics and mRNA expression level on the prognosis of breast cancer patients.
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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. 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