Cuproptosis-associated ncRNAs predict breast cancer subtypes

Cuproptosis is a novel copper-dependent mode of cell death that has recently been discovered. The relationship between Cuproptosis-related ncRNAs and breast cancer subtypes, however, remains to be studied. The aim of this study was to construct a breast cancer subtype prediction model associated wit...

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Published inPloS one Vol. 19; no. 2; p. e0299138
Main Authors Xia, Qing, Shen, Jinze, Wang, Qurui, Chen, Ruixiu, Zheng, Xinying, Yan, Qibin, Du, Lihua, Li, Hanbing, Duan, Shiwei
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 26.02.2024
Public Library of Science (PLoS)
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Summary:Cuproptosis is a novel copper-dependent mode of cell death that has recently been discovered. The relationship between Cuproptosis-related ncRNAs and breast cancer subtypes, however, remains to be studied. The aim of this study was to construct a breast cancer subtype prediction model associated with Cuproptosis. This model could be used to determine the subtype of breast cancer patients. To achieve this aim, 21 Cuproptosis-related genes were obtained from published articles and correlation analysis was performed with ncRNAs differentially expressed in breast cancer. Random forest algorithms were subsequently utilized to select important ncRNAs and build breast cancer subtype prediction models. A total of 94 ncRNAs significantly associated with Cuproptosis were obtained and the top five essential features were chosen to build a predictive model. These five biomarkers were differentially expressed in the five breast cancer subtypes and were closely associated with immune infiltration, RNA modification, and angiogenesis. The random forest model constructed based on Cuproptosis-related ncRNAs was able to accurately predict breast cancer subtypes, providing a new direction for the study of clinical therapeutic targets.
Bibliography:ObjectType-Article-1
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Competing Interests: The authors have declared that no competing interest exists.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0299138