Cargando…

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:...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Lishan, Xu, Chaojie, Zhang, Tong, Chen, Shengyang, Hu, Shuiquan, Cheng, Bingbing, Tong, Hao, Li, Xiaoyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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
_version_ 1784812889677234176
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
work_keys_str_mv AT songlishan clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma
AT xuchaojie clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma
AT zhangtong clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma
AT chenshengyang clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma
AT hushuiquan clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma
AT chengbingbing clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma
AT tonghao clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma
AT lixiaoyong clinicalneutrophilassociatedgenesasreliablepredictorsofhepatocellularcarcinoma