Cancer Research Center, School of Medicine, Xiamen University, 4221 Xiang'an South Road, Xiamen 361102, China.
Department of Gastroenterology, School of medicine, Xiamen University, 4221 Xiang'an South Road, Xiamen 361102, China.
Int J Mol Sci. 2023 Feb 9;24(4):3486. doi: 10.3390/ijms24043486.
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.
空泡分选相关蛋白 26A(VPS26A)是肝细胞癌的候选预后基因,但它在胰腺导管腺癌(PAAD)中的表达和功能尚不清楚。本研究通过生物信息学和免疫组织化学分析探讨和验证了 VPS26A 在 PAAD 中的 mRNA 和蛋白表达。评估了 VPS26A 表达与各种临床参数、遗传状态、诊断和预后价值、生存和免疫浸润的相关性,并对 VPS26A 的共表达基因集富集分析进行了评估。细胞学和分子实验进一步研究了 VPS26A 在 PAAD 中的作用和潜在机制。VPS26A 的 mRNA 和蛋白水平在 PAAD 组织中升高。高 VPS26A 表达与组织学类型较晚、肿瘤分期简化、吸烟状态和肿瘤突变负担评分有关,且与 PAAD 患者的不良预后相关。VPS26A 表达与免疫浸润和免疫治疗反应显著相关。VPS26A 共表达基因主要富集在细胞黏附及肌动蛋白细胞骨架调控和免疫反应调节信号通路。我们的实验进一步表明,VPS26A 通过激活 EGFR/ERK 信号通路促进 PAAD 细胞系的增殖、迁移和侵袭能力。本研究表明,VPS26A 可以通过全面调节其生长、迁移和免疫微环境,成为 PAAD 的潜在生物标志物和治疗靶点。