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Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma
Background: Growing evidence suggests that infiltrating neutrophils are key players in hepatocellular carcinoma (HCC) tumor progression. However, a comprehensive analysis of the biological roles of neutrophil infiltration and related genes in clinical outcomes and immunotherapy is lacking. Methods:...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582652/ https://www.ncbi.nlm.nih.gov/pubmed/36276937 http://dx.doi.org/10.3389/fgene.2022.989779 |
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author | Song, Lishan Xu, Chaojie Zhang, Tong Chen, Shengyang Hu, Shuiquan Cheng, Bingbing Tong, Hao Li, Xiaoyong |
author_facet | Song, Lishan Xu, Chaojie Zhang, Tong Chen, Shengyang Hu, Shuiquan Cheng, Bingbing Tong, Hao Li, Xiaoyong |
author_sort | Song, Lishan |
collection | PubMed |
description | Background: Growing evidence suggests that infiltrating neutrophils are key players in hepatocellular carcinoma (HCC) tumor progression. However, a comprehensive analysis of the biological roles of neutrophil infiltration and related genes in clinical outcomes and immunotherapy is lacking. Methods: HCC samples were obtained from the TCGA and GEO databases. The CIBERSORT algorithm was used to reveal the TIME landscape. Gene modules significantly associated with neutrophils were found using weighted gene co-expression network analysis (WGCNA), a “dynamic tree-cut” algorithm, and Pearson correlation analysis. Genes were screened using Cox regression analysis and LASSO and prognostic value validation was performed using Kaplan-Meier curves and receiver operating characteristic (ROC) curves. Risk scores (RS) were calculated and nomograms were constructed incorporating clinical variables. Gene set variation analysis (GSVA) was used to calculate signaling pathway activity. Immunophenoscore (IPS) was used to analyze differences in immunotherapy among samples with different risk scores. Finally, the relationship between RS and drug sensitivity was explored using the pRRophetic algorithm. Results: 10530 genes in 424 samples (50 normal samples, 374 tumor samples) were obtained from the TCGA database. Using WGCNA, the “MEbrown” gene module was most associated with neutrophils. Nine genes with prognostic value in HCC (PDLIM3, KLF2, ROR2, PGF, EFNB1, PDZD4, PLN, PCDH17, DOK5) were finally screened. Prognostic nomograms based on RS, gender, tumor grade, clinical stage, T, N, and M stages were constructed. The nomogram performed well after calibration curve validation. There is an intrinsic link between risk score and TMB and TIME. Samples with different risk scores differed in different signaling pathway activity, immunopharmaceutical treatment and chemotherapy sensitivity. Conclusion: In conclusion, a comprehensive analysis of neutrophil-related prognostic features will help in prognostic prediction and advance individualized treatment. |
format | Online Article Text |
id | pubmed-9582652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95826522022-10-21 Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma Song, Lishan Xu, Chaojie Zhang, Tong Chen, Shengyang Hu, Shuiquan Cheng, Bingbing Tong, Hao Li, Xiaoyong Front Genet Genetics Background: Growing evidence suggests that infiltrating neutrophils are key players in hepatocellular carcinoma (HCC) tumor progression. However, a comprehensive analysis of the biological roles of neutrophil infiltration and related genes in clinical outcomes and immunotherapy is lacking. Methods: HCC samples were obtained from the TCGA and GEO databases. The CIBERSORT algorithm was used to reveal the TIME landscape. Gene modules significantly associated with neutrophils were found using weighted gene co-expression network analysis (WGCNA), a “dynamic tree-cut” algorithm, and Pearson correlation analysis. Genes were screened using Cox regression analysis and LASSO and prognostic value validation was performed using Kaplan-Meier curves and receiver operating characteristic (ROC) curves. Risk scores (RS) were calculated and nomograms were constructed incorporating clinical variables. Gene set variation analysis (GSVA) was used to calculate signaling pathway activity. Immunophenoscore (IPS) was used to analyze differences in immunotherapy among samples with different risk scores. Finally, the relationship between RS and drug sensitivity was explored using the pRRophetic algorithm. Results: 10530 genes in 424 samples (50 normal samples, 374 tumor samples) were obtained from the TCGA database. Using WGCNA, the “MEbrown” gene module was most associated with neutrophils. Nine genes with prognostic value in HCC (PDLIM3, KLF2, ROR2, PGF, EFNB1, PDZD4, PLN, PCDH17, DOK5) were finally screened. Prognostic nomograms based on RS, gender, tumor grade, clinical stage, T, N, and M stages were constructed. The nomogram performed well after calibration curve validation. There is an intrinsic link between risk score and TMB and TIME. Samples with different risk scores differed in different signaling pathway activity, immunopharmaceutical treatment and chemotherapy sensitivity. Conclusion: In conclusion, a comprehensive analysis of neutrophil-related prognostic features will help in prognostic prediction and advance individualized treatment. Frontiers Media S.A. 2022-10-06 /pmc/articles/PMC9582652/ /pubmed/36276937 http://dx.doi.org/10.3389/fgene.2022.989779 Text en Copyright © 2022 Song, Xu, Zhang, Chen, Hu, Cheng, Tong and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Song, Lishan Xu, Chaojie Zhang, Tong Chen, Shengyang Hu, Shuiquan Cheng, Bingbing Tong, Hao Li, Xiaoyong Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma |
title | Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma |
title_full | Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma |
title_fullStr | Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma |
title_full_unstemmed | Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma |
title_short | Clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma |
title_sort | clinical neutrophil-associated genes as reliable predictors of hepatocellular carcinoma |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582652/ https://www.ncbi.nlm.nih.gov/pubmed/36276937 http://dx.doi.org/10.3389/fgene.2022.989779 |
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