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pmid:39448672

Identification of SLC31A1 as a prognostic biomarker and a target for therapeutics in breast cancer.

Hongtao Fu · Shanshan Dong · Kun Li

Scientific reports · 2024 doi:10.1038/s41598-024-76162-x

Paper

complete

Experiment

complete

Data

partial

Analysis

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title
Identification of SLC31A1 as a prognostic biomarker and a target for therapeutics in breast cancer.
doi
10.1038/s41598-024-76162-x
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39448672
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Hongtao Fu
[1]
Shanshan Dong
[2]
Kun Li
journal
Scientific reports
year
2024
abstract
Copper-induced cell death is regulated through protein lipoylation, which is critical for gene expression and phenotypic regulation. Neverless, the role of Cuproptosis-related genes in breast cancer (BC) remains unknown. This study aimed to construct a prognostic signature based on the expression of Cuproptosis-related genes in order to guide the diagnosis and treatment for BC. Cuproptosis-related genes prognostic signature has ata of 1250 BC tissues and 583 normal breast tissues were obtained from The Cancer Genome Atlas (TCGA), Genotype Tissue Expression (GTEx), and GEO GSE65212. The prognostic signature was established and evaluated with nineteen Cuproptosis-related genes. A series of in silico analyses based on SLC31A1, included expression analysis, independent prognostic analysis, correlation analysis, immune-related analysis and survival analysis. Finally, a series of cell experiments (including quantitative real-time polymerase chain reaction and western blot), and mice experiments were applied to evaluate the impact of SLC31A1 on BC. Cuproptosis-related genes prognostic signature has good predictive promising for survival in BC patients. We discovered that SLC31A1SLC31A1 was overexpressed in BC and was its independent prognostic factor. High expression of the SLC31A1 was correlated with poor prognosis and immune infiltrating of BC. SLC31A1 expression is associated with immune, chemotherapeutic and targeted therapy outcomes in BC. The proliferation, migration, and invasiveness of Her2 + enriched BC cells were decreased by SLC31A1 knockdown, also resulting in a decrease in tumor volume in mouse model. SLC31A1 is a candidate biomarker or therapeutic target in precision oncology, with diagnostic and prognostic significance in BC.
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We performed through multivariate cox regression analysis and then iterative analysis through step function to obtain the prognosis model. We used log rank and univariate Cox regression to compare the difference in survival between two or more groups, and performed timeROC (v 0.4) analysis to determine the accuracy of the discriminant prediction model.
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sections[5] "Cuproptosis-related genes prognostic model" paragraph 2
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We performed through multivariate cox regression analysis and then iterative analysis through step function to obtain the prognosis model. We used log rank and univariate Cox regression to compare the difference in survival between two or more groups, and performed timeROC (v 0.4) analysis to determine the accuracy of the discriminant prediction model.
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sections[42] "notes" paragraph 1
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The datasets generated and analysed during the current study are available in the TCGA repository (https://portal.gdc.cancer.gov/), GEO (GSE65212, http://www.ncbi.nlm.nih.gov/geo).
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The low-risk subgroup had better survival outcomes than the high-risk subgroup (p = 7.84e-06).
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K-M survival curves showed that the outcomes of BC cases in the low-risk subgroup were better than those with high-risk (p = 7.84e-06) (Fig. 1B, d).
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sections[25] "Construction of a prognostic signature in cuproptosis-related genes" paragraph 2
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K-M survival curves showed that the outcomes of BC cases in the low-risk subgroup were better than those with high-risk (p = 7.84e-06) (Fig. 1B, d).
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Expression profiling of breast cancer samples from Institut Curie (Maire cohort) -- BrainArray CDF
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enriched BC cells were decreased by SLC31A1 knockdown, also resulting in a decrease in tumor volum
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Methods Cell culture and transfection Cell line were from the Chinese Academy of S
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o resulting in a decrease in tumor volume in mouse model. SLC31A1 is a candidate biomarker or therape
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We performed through multivariate cox regression analysis and then iterative analysis through step function to obtain the prognosis model. We used log rank and univariate Cox regression to compare the difference in survival between two or more groups, and performed timeROC (v 0.4) analysis to determine the accuracy of the discriminant prediction model.
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This study aimed to construct a prognostic signature based on the expression of Cuproptosis-related genes in order to guide the diagnosis and treatment for BC. Cuproptosis-related genes prognostic signature has ata of 1250 BC tissues and 583 normal breast tissues were obtained from The Cancer Genome Atlas (TCGA), Genotype Tissue Expression (GTEx), and GEO GSE65212. The prognostic signature was established and evaluated with nineteen Cuproptosis-related genes. A series of in silico analyses based on SLC31A1, included expression analysis, independent prognostic analysis, correlation analysis, immune-related analysis and survival analysis. Finally, a series of cell experiments (including quantitative real-time polymerase chain reaction and western blot), and mice experiments were applied to evaluate the impact of SLC31A1 on BC. Cuproptosis-related genes prognostic signature has good predictive promising for survival in BC patients. We discovered that SLC31A1SLC31A1 was overexpressed in BC and was its independent prognostic factor. High expression of the SLC31A1 was correlated with poor prognosis and immune infiltrating of BC. SLC31A1 expression is associated with immune, chemotherapeutic and targeted therapy outcomes in BC. The proliferation, migration, and invasiveness of Her2 + enriched BC cells were decreased by SLC31A1 knockdown, also resulting in a decrease in tumor volume in mouse model. SLC31A1 is a candidate biomarker or therapeutic target in precision oncology, with diagnostic and prognostic significance in BC.", "claims": [{"id": "claim-method", "statement": "We performed through multivariate cox regression analysis and then iterative analysis through step function to obtain the prognosis model. 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