Suscribirse

Development and Verification of a novel cuproptosis- and immune-associated based prognostic genetic signature for pancreatic ductal adenocarcinoma - 02/03/23

Doi : 10.1016/j.clinre.2023.102089 
Xiang Xu 1, Jia-Hua Liang 1, Qiong-Cong Xu, Xiao-Yu Yin
 Department of Pancreato-Biliary Surgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, Guangdong, China 

Corresponding author at: Department of Pancreato-Biliary Surgery, The First Affiliated Hospital, Sun Yat-sen University, 58 Zhongshan 2nd Rd, Guangzhou 510080, Guangdong, China.Department of Pancreato-Biliary SurgeryThe First Affiliated HospitalSun Yat-sen University58 Zhongshan 2nd RdGuangzhouGuangdong510080China

Highlights

Construction of a cuproptosis- and immune-associated prognostic model for PDAC patients.
Cuproptosis might affect the prognosis of PDAC patients via regulating the tumor immune microenvironment.
Cuproptosis might be a promising therapeutic target for PDAC.

El texto completo de este artículo está disponible en PDF.

Abstract

Objective

Pancreatic ductal adenocarcinoma (PDAC) is a malignancy with a dismal prognosis. Cuproptosis, a novel mechanism mediated by protein lipoylation, results in acute proteotoxic stress and ultimately cell death. However, the clinical impacts of cuproptosis-associated genes and their relationship with immune status in PDAC have not been documented. In this study, we aimed at constructing a cuproptosis- and immune-associated prognostic signature to stratify and predict the prognosis for PDAC patients.

Methods

The gene expression profiles of 176 PDAC patients from The Cancer Genome Atlas and 167 normal pancreas tissues from the Genotype-Tissue Expression Project were analyzed for differentially expressed genes (DEGs) between PDAC and normal tissues. Pearson correlation analyses were performed to screen out cuproptosis- and immune-associated DEGs. The risk signature of DEGs was constructed using the least absolute shrinkage and selection operator (LASSO) Cox regression analysis, which was validated in the Gene Expression Omnibus (GEO) cohort (n = 114). The immune characteristics in the two risk groups were evaluated using single-sample gene set enrichment analysis and ESTIMATE algorithms.

Results

A total of 91 cuproptosis- and immune-associated DEGs were screened out, and eight prognostic-related genes were identified using LASSO Cox regression. The prognostic-related genes were then used to construct a risk scoring model, which stratified patients into low- and high-risk groups and were further verified in the external GEO database. The patients in the high-risk group had significantly shorter overall survival than those in the low-risk group. A nomogram based on the risk signature was then constructed. Immune infiltration evaluation suggested that immune status was more activated in the low-risk group. The mutation spectrum also differed between high- and low-risk groups.

Conclusions

Our cuproptosis- and immune-associated genetic risk signature could be a prognostic biomarker for PDAC. Cuproptosis might be a promising therapeutic target for PDAC.

El texto completo de este artículo está disponible en PDF.

Keywords : Pancreatic ductal adenocarcinoma, Cuproptosis, Prognosis, immune

Abbreviations : AUC, DEGs, GEO, GO, GSEA, GTEx, KEGG, LASSO, OS, PDAC, ROC, ssGSEA, TADCs, TCA, TCGA, TNM


Esquema


© 2023  Publicado por Elsevier Masson SAS.
Añadir a mi biblioteca Eliminar de mi biblioteca Imprimir
Exportación

    Exportación citas

  • Fichero

  • Contenido

Vol 47 - N° 3

Artículo 102089- mars 2023 Regresar al número
Artículo precedente Artículo precedente
  • Sensitivity of fecal immunochemical test and risk factors for interval colorectal cancer in a French population
  • Mikaël Canévet, Manon Pruvost-Couvreur, Marie Morvan, Bogdan Badic, Josiane Brousse-Potocki, Tiphaine Kermarrec, Servane Bouzeloc, Jean-Baptiste Nousbaum, Michel Robaszkiewicz, Noémi Reboux, Lucille Quénéhervé
| Artículo siguiente Artículo siguiente
  • Prognostic and predictive value of tumoral DNA damage repair protein expression in patients with resected pancreatic cancer
  • Furkan Ceylan, Deniz Can Guven, Hakan Taban, Oktay Aktepe, Taha Koray Sahin, Sadettin Kilickap, Alev Turker, Erhan Hamaloglu, Derya Karakoc, Aynur Isik, Aytekin Akyol, Suayib Yalcin, Omer Dizdar

Bienvenido a EM-consulte, la referencia de los profesionales de la salud.
El acceso al texto completo de este artículo requiere una suscripción.

¿Ya suscrito a @@106933@@ revista ?

Mi cuenta


Declaración CNIL

EM-CONSULTE.COM se declara a la CNIL, la declaración N º 1286925.

En virtud de la Ley N º 78-17 del 6 de enero de 1978, relativa a las computadoras, archivos y libertades, usted tiene el derecho de oposición (art.26 de la ley), el acceso (art.34 a 38 Ley), y correcta (artículo 36 de la ley) los datos que le conciernen. Por lo tanto, usted puede pedir que se corrija, complementado, clarificado, actualizado o suprimido información sobre usted que son inexactos, incompletos, engañosos, obsoletos o cuya recogida o de conservación o uso está prohibido.
La información personal sobre los visitantes de nuestro sitio, incluyendo su identidad, son confidenciales.
El jefe del sitio en el honor se compromete a respetar la confidencialidad de los requisitos legales aplicables en Francia y no de revelar dicha información a terceros.


Todo el contenido en este sitio: Copyright © 2024 Elsevier, sus licenciantes y colaboradores. Se reservan todos los derechos, incluidos los de minería de texto y datos, entrenamiento de IA y tecnologías similares. Para todo el contenido de acceso abierto, se aplican los términos de licencia de Creative Commons.