Wang Jun, Chu Yueming, Hu Guangbing, Liang Shiqi, Cui Yutong, Zuo Ji, Luo Zichen, Chen Xinrui, Wang Xiaobo, Yu Zhenghang, Zhang Zhongyang, Wang Xianfei
Department of Gastroenterology, Affiliated Hospital of North Sichuan Medical College, Nanchong, 637000, Sichuan, China.
School of Pharmacy, North Sichuan Medical College, Nanchong, 637000, Sichuan, China.
Biochem Genet. 2025 May 18. doi: 10.1007/s10528-025-11139-7.
To examine the impact of Piperlongumine (PL) on the proliferation, migration, invasion, cell cycle progression, and apoptosis in esophageal squamous cell carcinoma (ESCC) cells, as well as to elucidate the underlying molecular mechanisms. The suppressive effects of PL on the viability of ESCC cells were assessed using the CCK-8 assay, bright field imaging, and colony formation assays. Apoptosis induction and cell cycle disruption by PL were evaluated using flow cytometry. The impact of PL on ESCC cell migration and invasion was examined through scratch healing and Transwell assays. Differential gene expression analysis of ESCC tumor and normal tissues from the GSE29886 dataset, integrated with network pharmacology predictions, was conducted to identify core genes and molecular mechanisms involved in PL action. Key protein expression levels in the apoptosis, epithelial-mesenchymal transition (EMT), and PI3K/AKT signaling pathways were quantified by Western blotting. The CCK-8 and colony formation assays demonstrated that PL effectively suppressed cell viability and proliferation in ESCC. Flow cytometry revealed that PL down-regulated CDK1 expression, resulting in G2/M phase arrest, and promoted apoptosis by decreasing Bcl-2 levels and increasing cleaved caspase-3 and PARP. The scratch and Transwell assays indicated that PL inhibited ESCC cell migration and invasion, down-regulated the EMT-associated proteins Vimentin and N-cadherin, and up-regulated E-cadherin. Western blotting confirmed the down-regulation of P-PI3K and P-AKT, indicating the inhibition of the PI3K/AKT pathway by PL. These findings offer a pharmacological foundation for the development of PL as a potential phytotherapeutic agent for the clinical management of ESCC.
研究胡椒碱(PL)对食管鳞状细胞癌(ESCC)细胞增殖、迁移、侵袭、细胞周期进程及凋亡的影响,并阐明其潜在的分子机制。采用CCK-8法、明场成像和集落形成试验评估PL对ESCC细胞活力的抑制作用。使用流式细胞术评估PL诱导的凋亡和细胞周期紊乱。通过划痕愈合试验和Transwell试验检测PL对ESCC细胞迁移和侵袭的影响。结合网络药理学预测,对GSE29886数据集中ESCC肿瘤组织和正常组织进行差异基因表达分析,以确定参与PL作用的核心基因和分子机制。通过蛋白质免疫印迹法对凋亡、上皮-间质转化(EMT)和PI3K/AKT信号通路中的关键蛋白表达水平进行定量分析。CCK-8和集落形成试验表明,PL能有效抑制ESCC细胞的活力和增殖。流式细胞术显示,PL下调CDK1表达,导致G2/M期阻滞,并通过降低Bcl-2水平、增加裂解的caspase-3和PARP促进凋亡。划痕试验和Transwell试验表明,PL抑制ESCC细胞迁移和侵袭,下调与EMT相关的蛋白波形蛋白和N-钙黏蛋白,并上调E-钙黏蛋白。蛋白质免疫印迹法证实P-PI3K和P-AKT下调,表明PL抑制PI3K/AKT通路。这些发现为将PL开发成为用于ESCC临床治疗的潜在植物治疗剂提供了药理学依据。