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TSPAN1, TMPRSS4, SDR16C5, and CTSE as Novel Panel for Pancreatic Cancer: A Bioinformatics Analysis and Experiments Validation

胰腺癌 恶性肿瘤 基因 医学 生物信息学 肿瘤科 基因表达谱 内科学 免疫组织化学 癌症 生物 基因表达 病理 遗传学
作者
Yi-Jun Hua,Tiandong Li,Hua Wang,Jinyu Wu,Chuncheng Yi,Jianxiang Shi,Peng Wang,Chunhua Song,Liping Dai,Guozhong Jiang,Yuguang Huang,Yu Ye,Jitian Li
出处
期刊:Frontiers in Immunology [Frontiers Media]
卷期号:12 被引量:18
标识
DOI:10.3389/fimmu.2021.649551
摘要

Pancreatic cancer is a lethal malignancy with a poor prognosis. This study aims to identify pancreatic cancer-related genes and develop a robust diagnostic model to detect this disease. Weighted gene co-expression network analysis (WGCNA) was used to determine potential hub genes for pancreatic cancer. Their mRNA and protein expression levels were validated through reverse transcription PCR (RT-PCR) and immunohistochemical (IHC). Diagnostic models were developed by eight machine learning algorithms and ten-fold cross-validation. Four hub genes ( TSPAN1, TMPRSS4, SDR16C5 , and CTSE ) were identified based on bioinformatics. RT-PCR showed that the four hub genes were expressed at medium to high levels, IHC revealed that their protein expression levels were higher in pancreatic cancer tissues. For the panel of these four genes, eight models performed with 0.87–0.92 area under the curve value (AUC), 0.91–0.94 sensitivity, and 0.84–0.86 specificity in the validation cohort. In the external validation set, these models also showed good performance (0.86–0.98 AUC, 0.84–1.00 sensitivity, and 0.86–1.00 specificity). In conclusion, this study has identified four hub genes that might be closely related to pancreatic cancer: TSPAN1, TMPRSS4, SDR16C5 , and CTSE . Four-gene panels might provide a theoretical basis for the diagnosis of pancreatic cancer.

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