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pmid:35831362

Pancreatic adenocarcinoma associated immune-gene signature as a novo risk factor for clinical prognosis prediction in hepatocellular carcinoma.

Lei Dai · Joseph Mugaanyi · Xingchen Cai · Caide Lu · Changjiang Lu

Scientific reports · 2022 doi:10.1038/s41598-022-16155-w

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

Execution evidence has not yet been added to this .science file. Explore its methods, data and open questions to plan the next step.
Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:35831362
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science-record
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2026-11-01T18:14:53Z
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2026-11-01T22:07:01Z
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paper object · 10 fields
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title
Pancreatic adenocarcinoma associated immune-gene signature as a novo risk factor for clinical prognosis prediction in hepatocellular carcinoma.
doi
10.1038/s41598-022-16155-w
pmid
35831362
authors array · 5 items
[0]
Lei Dai
[1]
Joseph Mugaanyi
[2]
Xingchen Cai
[3]
Caide Lu
[4]
Changjiang Lu
journal
Scientific reports
year
2022
abstract
Pancreatic adenocarcinoma (PAAD) has high mortality and a very poor prognosis. Both surgery and chemotherapy have a suboptimal therapeutic effect, and this caused a need to find new approaches such as immunotherapy. Therefore, it is essential to develop a new model to predict patient prognosis and facilitate early intervention. Our study screened out and validated the target molecules based on the TCGA-PAAD dataset. We established the risk signature using univariate and multivariate Cox regression analysis and used GSE62452 and GSE28735 to verify the accuracy and reliability of the model. Expanded application of PAAD-immune-related genes signature (-IRGS) on other datasets was conducted, and the corresponding nomograms were constructed. We also analyzed the correlation between immune-related cells/genes and potential treatments. Our research demonstrated that a high riskscore of PAAD-IRGS in patients with PAAD was correlated with poor overall survival, disease-specific survival and progression free interval. The same results were observed in patients with LIHC. The models constructed were confirmed to be accurate and reliable. We found various correlations between PAAD-IRGS and immune-related cells/genes, and the potential therapeutic agents. These findings indicate that PAAD-IRGS may be a promising indicator for prognosis and of the tumor-immune microenvironment status in PAAD.
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Based on the gene analysis above, we obtained independent immune-related prognostic risk genes using the Least absolute shrinkage and selection operator (Lasso) regression analysis29, followed by univariate and multivariate Cox regression analysis for further identification.
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sections[6] "Construction of PAAD-related IRGs signature (PAAD-IRGS) for prognosis" paragraph 2
quote
Based on the gene analysis above, we obtained independent immune-related prognostic risk genes using the Least absolute shrinkage and selection operator (Lasso) regression analysis29, followed by univariate and multivariate Cox regression analysis for further identification.
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The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author/s. All data and original files in our work are freely available under a ‘Creative Commons BY 4.0’ license. All methods were carried out in accordance with relevant guidelines and regulations.
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sections[27] "Data availability" paragraph 2
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The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author/s. All data and original files in our work are freely available under a ‘Creative Commons BY 4.0’ license. All methods were carried out in accordance with relevant guidelines and regulations.
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The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author/s. All data and original files in our work are freely available under a ‘Creative Commons BY 4.0’ license. All methods were carried out in accordance with relevant guidelines and regulations.
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Microarray gene-expression profiles of 45 matching pairs of pancreatic tumor and adjacent non-tumor tissues from 45 patients with pancreatic ductal adenocarcinoma
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The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author/s. All data and original files in our work are freely available under a ‘Creative Commons BY 4.0’ license. All methods were carried out in accordance with relevant guidelines and regulations.
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Microarray gene-expression profiles of 69 pancreatic tumors and 61 adjacent non-tumor tissue from patients with pancreatic ductal adenocarcinoma
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Based on the gene analysis above, we obtained independent immune-related prognostic risk genes using the Least absolute shrinkage and selection operator (Lasso) regression analysis29, followed by univariate and multivariate Cox regression analysis for further identification.
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The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author/s. All data and original files in our work are freely available under a ‘Creative Commons BY 4.0’ license. All methods were carried out in accordance with relevant guidelines and regulations.
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cytoplasmic and nuclear staining (Fig.S1A). Immunohistochemistry (IHC) results also confirmed that S100P was
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ar staining (Fig.S1A). Immunohistochemistry (IHC) results also confirmed that S100P was highl
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Based on the gene analysis above, we obtained independent immune-related prognostic risk genes using the Least absolute shrinkage and selection operator (Lasso) regression analysis29, followed by univariate and multivariate Cox regression analysis for further identification.
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Complete file
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Both surgery and chemotherapy have a suboptimal therapeutic effect, and this caused a need to find new approaches such as immunotherapy. Therefore, it is essential to develop a new model to predict patient prognosis and facilitate early intervention. Our study screened out and validated the target molecules based on the TCGA-PAAD dataset. We established the risk signature using univariate and multivariate Cox regression analysis and used GSE62452 and GSE28735 to verify the accuracy and reliability of the model. Expanded application of PAAD-immune-related genes signature (-IRGS) on other datasets was conducted, and the corresponding nomograms were constructed. We also analyzed the correlation between immune-related cells/genes and potential treatments. Our research demonstrated that a high riskscore of PAAD-IRGS in patients with PAAD was correlated with poor overall survival, disease-specific survival and progression free interval. The same results were observed in patients with LIHC. The models constructed were confirmed to be accurate and reliable. We found various correlations between PAAD-IRGS and immune-related cells/genes, and the potential therapeutic agents. 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