Titre :

Identification of pancreatic adenocarcinoma immune subtype associated with tumor neoantigen from aberrant alternative splicing

Auteur(s) :

Du, Qiong [Auteur]
Fudan University [Shanghai]
Yu, Zhan [Auteur]
Soochow University
Zhang, Zifeng [Auteur]
Fudan University [Shanghai]
Yang, Jianhui [Auteur]
Fudan University [Shanghai]
Jonckheere, Nicolas [Auteur]
Hétérogénéité, Plasticité et Résistance aux Thérapies des Cancers = Cancer Heterogeneity, Plasticity and Resistance to Therapies - UMR 9020 - U 1277 [CANTHER]
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
Shi, Si [Auteur]
Fudan University [Shanghai]
Wang, Wei [Auteur]
Fudan University [Shanghai]
Xu, Jin [Auteur]
Fudan University [Shanghai]
Liu, Jiyong [Auteur]
Yu, Xianjun [Auteur]
Fudan University [Shanghai]

Titre de la revue :

Journal of Gastrointestinal Oncology

Pagination :

1179-1197

Date de publication :

2024-06

ISSN :

2078-6891

Mot(s)-clé(s) en anglais :

Pancreatic adenocarcinoma (PAAD)
alternative splicing
immune microenvironment
neoantigen

Discipline(s) HAL :

Sciences du Vivant [q-bio]/Cancer

Résumé en anglais : [en]

Background: Pancreatic adenocarcinoma (PAAD) is referred to as an immunologically “cold” tumor that responds poorly to immunotherapy. A fundamental theory that explains the low immunogenicity of PAAD is the dramatically ...
Lire la suite >Background: Pancreatic adenocarcinoma (PAAD) is referred to as an immunologically “cold” tumor that responds poorly to immunotherapy. A fundamental theory that explains the low immunogenicity of PAAD is the dramatically low tumor mutation burden (TMB) of PAAD tumors, which fails to induce sufficient immune response. Alternative splicing of pre-mRNA, which could alter the proteomic diversity of many cancers, has been reported to be involved in neoantigen production. Therefore, we aim to identify novel PAAD antigens and immune subtypes through systematic bioinformatics research.Methods: Data for splicing analysis were downloaded from The Cancer Genome Atlas (TCGA) SpliceSeq database. Among the available algorithms, we chose CIBERSORT to evaluate the immune cell distribution among PAADs. The TCGA-PAAD expression matrix was used to construct a co-expression network. Single-cell analysis was performed based on the Seurat workflow.Results: Integrated analysis of aberrantly upregulated genes, alternatively spliced genes, genes associated with nonsense-mediated RNA decay (NMD) factors, antigen presentation and overall survival (OS) in TCGA-PAAD revealed that PLEC is a promising neoantigen for PAAD-targeted therapy. We identified a C2 TCGA-PAAD subtype that had better prognosis and more CD8+ T-cell infiltration. We propose a novel immune subtyping system for PAAD to indicate patient prognosis and opportunities for immunotherapy, such as immune checkpoint (ICP) inhibitors.Conclusions: In conclusion, the present study used a transcriptome-guided approach to screen neoantigen candidates based on alternative splicing, NMD factors, and antigen-presenting signatures for PAAD. A prognosis model with guidance of immunotherapy will aid in patient selection for appropriate treatment.Lire moins >

Langue :

Anglais

Comité de lecture :

Oui

Audience :

Internationale

Vulgarisation :

Non

Collections :

• Cancer Heterogeneity, Plasticity and Resistance to Therapies (CANTHER) - UMR 9020 - UMR 1277

Source :

Harvested from HAL