A novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma

Abstract Pyroptosis is an inflammatory form of cell death, which plays a key role in the development of auto-inflammation and cancer. This study aimed to construct a pyroptosis and inflammasome-related genes for predicting prognosis of the pancreatic ductal adenocarcinoma (PDAC). This study was base...

Full description

Bibliographic Details
Main Authors: Jieliang Zuo, Chenhe Yi, Zhenmei Chen, Bo Zhou, Tingsong Yang, Jing Lin
Format: Article
Language:English
Published: Nature Portfolio 2022-11-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-22864-z
_version_ 1811328885921415168
author Jieliang Zuo
Chenhe Yi
Zhenmei Chen
Bo Zhou
Tingsong Yang
Jing Lin
author_facet Jieliang Zuo
Chenhe Yi
Zhenmei Chen
Bo Zhou
Tingsong Yang
Jing Lin
author_sort Jieliang Zuo
collection DOAJ
description Abstract Pyroptosis is an inflammatory form of cell death, which plays a key role in the development of auto-inflammation and cancer. This study aimed to construct a pyroptosis and inflammasome-related genes for predicting prognosis of the pancreatic ductal adenocarcinoma (PDAC). This study was based primarily on the one-way analysis of variance, univariate Cox regression analysis, Least absolute shrinkage and selection operator (LASSO) Cox regression, a risk-prognostic signature, gene set variation analysis (GSVA), and immune microenvironment analysis, using PDAC data from The Cancer Genome Atlas and International Cancer Genome Consortium databases for the analysis of the role of 676 pyroptosis and inflammasome-related genes in PDAC retrieved from the Reactome and GeneCards databases. Lastly, we collected six paired PDAC and matched normal adjacent tissue samples to verify the expression of signature genes by quantitative real-time PCR (qRT-PCR). We identified 18 candidate pyroptosis and inflammasome-related genes that differed significantly between pathologic grades (stages) of PDAC patients. The univariate Cox and LASSO analyses pointed to six genes as the best variables for constructing a prognostic signature, including ACTA2, C1QTNF9, DNAH8, GATM, LBP, and NGF. The results of the risk prognostic model indicated that the AUCs at 1, 3, and 5 years were greater than 0.62. GSVA revealed that ‘GLYCOLYSIS’, ‘P53 PATHWAY’, ‘KRAS SIGNALING UP’, and ‘INFLAMMATORY RESPONSE’ hallmark gene sets were associated with the risk score. The high-risk group was associated with poor prognosis and was characterized by a lower infiltration of cells involved in anti-tumor immunity; whereas the low-risk group with higher T cells, NK cells, and macrophages showed relatively better survival and significantly higher upregulation of cytolytic scores and inflammation scores. Additionally, crucial pyroptosis and inflammasome-related genes were further validated by qRT-PCR. Our study revealed the prognostic role of the pyroptosis and inflammasome-related genes in PDAC for the first time. Simultaneously, the biological and prognostic heterogeneity of PDAC had been demonstrated, deepening our molecular understanding of this tumor.
first_indexed 2024-04-13T15:34:09Z
format Article
id doaj.art-3cf9c31deb12472fb451090f1b9124af
institution Directory Open Access Journal
issn 2045-2322
language English
last_indexed 2024-04-13T15:34:09Z
publishDate 2022-11-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj.art-3cf9c31deb12472fb451090f1b9124af2022-12-22T02:41:19ZengNature PortfolioScientific Reports2045-23222022-11-0112111510.1038/s41598-022-22864-zA novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinomaJieliang Zuo0Chenhe Yi1Zhenmei Chen2Bo Zhou3Tingsong Yang4Jing Lin5Department of General Surgery, Shanghai Tenth People’s Hospital, Tongji University School of MedicineDepartment of General Surgery, Huashan Hospital, Fudan UniversityDepartment of General Surgery, Huashan Hospital, Fudan UniversityDepartment of General Surgery, Shanghai Tenth People’s Hospital, Tongji University School of MedicineDepartment of General Surgery, Shanghai Tenth People’s Hospital, Tongji University School of MedicineDepartment of General Surgery, Huashan Hospital, Fudan UniversityAbstract Pyroptosis is an inflammatory form of cell death, which plays a key role in the development of auto-inflammation and cancer. This study aimed to construct a pyroptosis and inflammasome-related genes for predicting prognosis of the pancreatic ductal adenocarcinoma (PDAC). This study was based primarily on the one-way analysis of variance, univariate Cox regression analysis, Least absolute shrinkage and selection operator (LASSO) Cox regression, a risk-prognostic signature, gene set variation analysis (GSVA), and immune microenvironment analysis, using PDAC data from The Cancer Genome Atlas and International Cancer Genome Consortium databases for the analysis of the role of 676 pyroptosis and inflammasome-related genes in PDAC retrieved from the Reactome and GeneCards databases. Lastly, we collected six paired PDAC and matched normal adjacent tissue samples to verify the expression of signature genes by quantitative real-time PCR (qRT-PCR). We identified 18 candidate pyroptosis and inflammasome-related genes that differed significantly between pathologic grades (stages) of PDAC patients. The univariate Cox and LASSO analyses pointed to six genes as the best variables for constructing a prognostic signature, including ACTA2, C1QTNF9, DNAH8, GATM, LBP, and NGF. The results of the risk prognostic model indicated that the AUCs at 1, 3, and 5 years were greater than 0.62. GSVA revealed that ‘GLYCOLYSIS’, ‘P53 PATHWAY’, ‘KRAS SIGNALING UP’, and ‘INFLAMMATORY RESPONSE’ hallmark gene sets were associated with the risk score. The high-risk group was associated with poor prognosis and was characterized by a lower infiltration of cells involved in anti-tumor immunity; whereas the low-risk group with higher T cells, NK cells, and macrophages showed relatively better survival and significantly higher upregulation of cytolytic scores and inflammation scores. Additionally, crucial pyroptosis and inflammasome-related genes were further validated by qRT-PCR. Our study revealed the prognostic role of the pyroptosis and inflammasome-related genes in PDAC for the first time. Simultaneously, the biological and prognostic heterogeneity of PDAC had been demonstrated, deepening our molecular understanding of this tumor.https://doi.org/10.1038/s41598-022-22864-z
spellingShingle Jieliang Zuo
Chenhe Yi
Zhenmei Chen
Bo Zhou
Tingsong Yang
Jing Lin
A novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma
Scientific Reports
title A novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma
title_full A novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma
title_fullStr A novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma
title_full_unstemmed A novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma
title_short A novel refined pyroptosis and inflammasome-related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma
title_sort novel refined pyroptosis and inflammasome related genes signature for predicting prognosis and immune microenvironment in pancreatic ductal adenocarcinoma
url https://doi.org/10.1038/s41598-022-22864-z
work_keys_str_mv AT jieliangzuo anovelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT chenheyi anovelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT zhenmeichen anovelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT bozhou anovelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT tingsongyang anovelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT jinglin anovelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT jieliangzuo novelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT chenheyi novelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT zhenmeichen novelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT bozhou novelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT tingsongyang novelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma
AT jinglin novelrefinedpyroptosisandinflammasomerelatedgenessignatureforpredictingprognosisandimmunemicroenvironmentinpancreaticductaladenocarcinoma