The role of PDIA3 in oral squamous cell carcinoma and its value as A diagnostic and prognostic biomarker

生物标志物 基因敲除 癌症研究 细胞凋亡 下调和上调 生物 活力测定 癌症 蛋白质二硫键异构酶 比例危险模型 肿瘤科 医学 内科学 基因 细胞生物学 生物化学 内质网
作者
Lin Wang,Xinxin Wang,Jia Zhang,Jiafeng Duan,Chengfang Tang,Linmei Zhang,Hui Zeng,H. Li,Yuefan Li,Yan Zhou
出处
期刊:Heliyon [Elsevier BV]
卷期号:9 (12): e22596-e22596
标识
DOI:10.1016/j.heliyon.2023.e22596
摘要

BackgroundThis study aimed to investigate the role of protein disulfide isomerase A3 (PDIA3) in oral squamous cell carcinoma (OSCC) and evaluate its significance as a diagnostic and prognostic biomarker.MethodsComprehensive bioinformatics analysis of the OSCC dataset from The Cancer Genome Atlas (TCGA) was performed. PDIA3 was depleted in CAL27 and SCC25 OSCC cells by transfection with PDIA3-specific siRNA oligos. The effects of PDIA3 downregulation on cell viability, apoptosis, and cell migration were evaluated using CCK8, ELISA, and wound healing assays, respectively.ResultsThe mRNA and protein expression of PDIA3 was significantly up-regulated in OSCC tissues compared to adjacent normal tissues. Knockdown of PDIA3 led to significantly decreased cell viability, increased apoptosis, and suppressed migratory ability in OSCC cells. The Kaplan-Meier survival curve showed that patients with higher PDIA3 expression levels had shorter survival than those with low PDIA3 levels. The receiver operating characteristic (ROC) curve indicated that PDIA3 had high sensitivity and accuracy for detecting OSCC (area under the curve (AUC): 0.917, CI: 0.879–0.955). Univariate and multivariate Cox regression analyses identified PDIA3 as an independent prognostic factor of OSCC. Furthermore, the depletion of PDIA3 inhibited AKT activity in OSCC cells. Gene set enrichment analysis (GSEA) indicated that PDIA3 is involved in various important biological functions and signaling pathways closely related to cancer development.ConclusionPDIA3 plays an oncogenic role in OSCC and represents a good candidate as a diagnostic and prognostic biomarker for OSCC.
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