Sun Y Q, Fu Y, Ji O X, Wang L J
Graduate Training Base of Jinzhou Medical University (Linyi People's Hospital), Linyi 276000, China Linyi Key Laboratory of Tumor Biology, Linyi People's Hospital, Linyi 276000, China Department of Hematology, Linyi People's Hospital, Key Laboratory of Tumor Translational Medicine, Xuzhou Medical University, Linyi 276000, China.
Linyi Key Laboratory of Tumor Biology, Linyi People's Hospital, Linyi 276000, China.
Zhonghua Xue Ye Xue Za Zhi. 2024 Apr 14;45(4):391-395. doi: 10.3760/cma.j.cn121090-20230831-00099.
The aim of this study was to investigate the effects of polyphyllin Ⅶ (PP Ⅶ) on proliferation, apoptosis, and cell cycle of diffuse large B-cell lymphoma (PLBCL) cell lines U2932 and SUDHL-4. The DLBCL cell lines were divided into a control group and a PPⅦ group, and experiments were conducted using MTT assay, flow cytometry, and Western blotting.Results showed that compared with the control group, PPⅦ significantly inhibited the proliferation of U2932 and SUDHL-4 cells (<0.05). Apoptosis assays demonstrated that treatment with 0.50 and 1.00 µmol/L PP Ⅶ significantly increased the apoptosis rates of both cell lines (<0.05), upregulated apoptosis-related proteins, and downregulated Bcl-2 protein level (<0.05). Cell cycle analysis revealed that PPⅦ treatment led to an increase in G0/G1-phase cells (<0.05) and a decrease in G2/M-phase cells (<0.05), significantly downregulated cyclin D1, CDK4, CDK6, and survivin protein expression (<0.05). In conclusion, PPⅦ exerted anti-lymphoma effects by inhibiting proliferation, promoting apoptosis, and inducing G0/G1 phase arrest in DLBCL cells.
本研究旨在探讨重楼皂苷Ⅶ(PPⅦ)对弥漫性大B细胞淋巴瘤(DLBCL)细胞系U2932和SUDHL-4增殖、凋亡及细胞周期的影响。将DLBCL细胞系分为对照组和PPⅦ组,并采用MTT法、流式细胞术和蛋白质免疫印迹法进行实验。结果显示,与对照组相比,PPⅦ显著抑制U2932和SUDHL-4细胞的增殖(P<0.05)。凋亡检测表明,0.50和1.00 μmol/L的PPⅦ处理显著提高了两种细胞系的凋亡率(P<0.05),上调了凋亡相关蛋白,并下调了Bcl-2蛋白水平(P<0.05)。细胞周期分析显示,PPⅦ处理导致G0/G1期细胞增加(P<0.05),G2/M期细胞减少(P<0.05),显著下调细胞周期蛋白D1、细胞周期蛋白依赖性激酶4(CDK4)、细胞周期蛋白依赖性激酶6(CDK6)和生存素蛋白表达(P<0.05)。综上所述,PPⅦ通过抑制DLBCL细胞增殖、促进凋亡和诱导G0/G1期阻滞发挥抗淋巴瘤作用。