Chen Yi, Wu Tong, Li Qi, Li Ming-Jie, Yu Na, Meng Li-Jueyi, Chen Xian-Jin, Chi Bang-Teng, Li Shi-De, Huang Su-Ning, Chen Gang, Ye Yu-Ping, Wei Dan-Ming
Department of Pathology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Department of Information Management and Information System, School of Information and Management, Guangxi Medical University, Nanning, China.
IET Syst Biol. 2025 Jan-Dec;19(1):e70017. doi: 10.1049/syb2.70017.
SAE1, a key factor in tumour development, has not been thoroughly examined in pancreatic adenocarcinoma (PAAD), a cancer with high incidence and poor prognosis. We conducted a comprehensive study, integrating mRNA data, immunohistochemistry, CRISPR-modified cell line analysis and single-cell RNA sequencing to assess SAE1's role in PAAD. We also used ChIP-Seq to explore SAE1's transcriptional regulation and analysed clinical data, drug sensitivity and molecular docking models. SAE1 mRNA was significantly overexpressed in PAAD, with a substantial impact on cell proliferation and migration. Functional analyses linked SAE1 to cell cycle and DNA replication pathways, suggesting a role in PAAD development. Our study indicates that SAE1 may promote PAAD through cell cycle pathways, with FOXA1 potentially regulating SAE1's abnormal behaviour.
SAE1是肿瘤发展的关键因素,在胰腺癌(PAAD)中尚未得到充分研究,胰腺癌是一种发病率高且预后不良的癌症。我们进行了一项综合研究,整合了mRNA数据、免疫组织化学、CRISPR修饰细胞系分析和单细胞RNA测序,以评估SAE1在PAAD中的作用。我们还使用染色质免疫沉淀测序(ChIP-Seq)来探索SAE1的转录调控,并分析了临床数据、药物敏感性和分子对接模型。SAE1 mRNA在PAAD中显著过表达,对细胞增殖和迁移有重大影响。功能分析将SAE1与细胞周期和DNA复制途径联系起来,表明其在PAAD发展中起作用。我们的研究表明,SAE1可能通过细胞周期途径促进PAAD,叉头框蛋白A1(FOXA1)可能调节SAE1的异常行为。