The Prognostic Value and the Oncogenic and Immunological Roles of Vacuolar Protein Sorting Associated Protein 26 A in Pancreatic Adenocarcinoma

Author:

Hou Jihuan1,Wu Han2,Xu Beibei1,Shang Jin1,Xu Xuechun1,Li Guixia1,Zhang Haoran1,Zhang Wenqing1,Deng Yabin1,Hong Xiaoting3ORCID,Hu Tianhui1ORCID,Zhang Mingqing2,Zhan Yanyan1

Affiliation:

1. Cancer Research Center, School of Medicine, Xiamen University, 4221 Xiang’an South Road, Xiamen 361102, China

2. Department of Gastroenterology, School of medicine, Xiamen University, 4221 Xiang’an South Road, Xiamen 361102, China

3. Department of Basic Medical Science, School of Medicine, Xiamen University, 4221 Xiang’an South Road, Xiamen 361102, China

Abstract

The identification of the prognostic markers and therapeutic targets might benefit the diagnosis and treatment of pancreatic adenocarcinoma (PAAD), one of the most aggressive malignancies. Vacuolar protein sorting associated protein 26 A (VPS26A) is a candidate prognosis gene for hepatocellular carcinoma, but its expression and function in PAAD remain unknown. The mRNA and protein expression of VPS26A in PAAD was explored and validated by bioinformatics and immunohistochemical analysis. The correlation between VPS26A expression and various clinical parameters, genetic status, diagnostic and prognostic value, survival and immune infiltration were evaluated, and the co-expressed gene-set enrichment analysis for VPS26A was performed. Cytologic and molecular experiments were further carried out to investigate the role and potential mechanism of VPS26A in PAAD. The mRNA and protein levels of VPS26A were elevated in PAAD tissues. High VPS26A expression was associated with the advanced histological type, tumor stage simplified, smoking status and tumor mutational burden score, and the poor prognosis of PAAD patients. VPS26A expression was significantly correlated with immune infiltration and immunotherapy response. VPS26A-co-expressed genes were mainly enriched in the regulation of cell adhesion and actin cytoskeleton and the immune-response-regulating signaling pathway. Our experiments further demonstrated that VPS26A promoted the proliferation, migration and invasion potentials of PAAD cell lines through activating the EGFR/ERK signaling. Our study suggested that VPS26A could be a potential biomarker and a therapeutic target for PAAD through comprehensive regulation of its growth, migration and immune microenvironment.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Xiamen

Natural Science Foundation of Fujian Province of China

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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