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pmid:39336730

UCN-Centric Prognostic Model for Predicting Overall Survival and Immune Response in Colorectal Cancer.

Jia Liu · Feiliang Zhong · Yue Chen

Genes · 2024 doi:10.3390/genes15091139

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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title
UCN-Centric Prognostic Model for Predicting Overall Survival and Immune Response in Colorectal Cancer.
doi
10.3390/genes15091139
pmid
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[0]
Jia Liu
[1]
Feiliang Zhong
[2]
Yue Chen
journal
Genes
year
2024
abstract
Colorectal cancer (CRC), a prevalent malignancy, ranks third in global incidence and second in mortality rates. Despite advances in screening methods such as colonoscopy, the accurate diagnosis of CRC remains challenging due to the absence of reliable biomarkers. This study aimed to develop a robust prognostic model for precise CRC outcome prediction. Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival. This gene panel facilitated accurate CRC outcome predictions, which is also validated via the external validation cohort GSE17536. We conducted further investigations into the key gene, urocortin (UCN), using single-cell transcriptomic data and immune infiltration analysis in CRC patients. Our results revealed a significant correlation between high UCN expression and the reduced prevalence of key immune cells, including B cells, CD4+ cytotoxic T cells, CD8+ T cells, and NKT cells. Functional experiments showed that UCN gene interference in the CRC cell lines significantly decreased cancer cell proliferation, underscoring UCN's role in intestinal immunity modulation. The UCN-centric prognostic model developed enhances prognosis prediction accuracy and offers critical insights for CRC diagnosis and therapeutic interventions.
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Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival.
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Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival.
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The bulk RNA-seq dataset TCGA-COAD was obtained from The Cancer Genome Atlas (https://portal.gdc.cancer.gov/, accessed on 1 January 2023). The bulk RNA-seq dataset GSE17536 was accessed from the GEO database (https://www.ncbi.nlm.nih.gov/geo, accessed on 15 January 2023). The CRC scRNA-seq dataset GSE161277 was also accessed from the GEO database (https://www.ncbi.nlm.nih.gov/geo, accessed on 15 January 2023). The data generated by this study are available from the Supplementary Materials. The R software packages utilized in this study are freely and open source. Source code for bulk RNA-seq and scRNA-seq are available at GitHub (https://github.com/liujialeo/Prognostic_model_of_COAD, accessed on 8 August 2023).
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The bulk RNA-seq dataset TCGA-COAD was obtained from The Cancer Genome Atlas (https://portal.gdc.cancer.gov/, accessed on 1 January 2023). The bulk RNA-seq dataset GSE17536 was accessed from the GEO database (https://www.ncbi.nlm.nih.gov/geo, accessed on 15 January 2023). The CRC scRNA-seq dataset GSE161277 was also accessed from the GEO database (https://www.ncbi.nlm.nih.gov/geo, accessed on 15 January 2023). The data generated by this study are available from the Supplementary Materials. The R software packages utilized in this study are freely and open source. Source code for bulk RNA-seq and scRNA-seq are available at GitHub (https://github.com/liujialeo/Prognostic_model_of_COAD, accessed on 8 August 2023).
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Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival.
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Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival.
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This gene panel facilitated accurate CRC outcome predictions, which is also validated via the external validation cohort GSE17536.
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Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival.
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label
Corpus assay engine
[1] object · 3 fields
id
agent:minimax-reader
type
software
label
MiniMax literature reader
source_run_id
reading-sci-2026-11-01
dsl_catalogue_fingerprint
343fb30756ba6ec3
capability_table_fingerprint
2cb3e42f047d2ecf
snapshot_id
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lineage object · 4 fields
parent_id
pmid:39336730
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fork_of
null
gaps array · 9 items
[0]
asset:data:geo:GSE161277 licence not read
[1]
asset:data:geo:GSE161277 not downloaded
[2]
asset:data:geo:GSE17536 licence not read
[3]
asset:data:geo:GSE17536 not downloaded
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execution.not_run
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method.reader_differs_from_extractor
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review.human_critique
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review.independent_reader
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review.machine_critique
assays array · 1 item
[0] object · 11 fields
role
analysis
definition_id
survival_analysis
definition_version
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required_operations array · 1 item
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cox_ph
support_state
supported
source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
[0]
Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival.
order_basis
analysis_only
id
assay:1
Complete file
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This study aimed to develop a robust prognostic model for precise CRC outcome prediction. Employing weighted co-expression network analysis (WGCNA) and Cox regression analysis on data from The Cancer Genome Atlas (TCGA), we identified a panel of 12 genes strongly associated with patient survival. This gene panel facilitated accurate CRC outcome predictions, which is also validated via the external validation cohort GSE17536. We conducted further investigations into the key gene, urocortin (UCN), using single-cell transcriptomic data and immune infiltration analysis in CRC patients. Our results revealed a significant correlation between high UCN expression and the reduced prevalence of key immune cells, including B cells, CD4+ cytotoxic T cells, CD8+ T cells, and NKT cells. Functional experiments showed that UCN gene interference in the CRC cell lines significantly decreased cancer cell proliferation, underscoring UCN's role in intestinal immunity modulation. 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