Department of Pharmacology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou 510080, P. R. China.
Biol Pharm Bull. 2012;35(8):1230-7. doi: 10.1248/bpb.b110535.
Panax Notoginseng Saponins (PNS) have been well known to have anti-tumor activity and enhance cytotoxicity of some cancer chemotherapy agents, but the mechanisms underlying these effects are still unknown. This study investigates the effect of PNS on cytotoxicity of cisplatin and the relationship between this effect and the modulation of gap junctions (GJ) function by PNS in a transfected cell line. The cytotoxicity of cisplatin (0.25-1 µg/mL) was increased in the presence of GJ. Inhibition of gap junction by either GJ blocker or interception of Connexin (Cx) expression decreased the cytotoxicity of cisplatin. Increasing GJ function enhanced cytotoxicity of cisplatin, only in the cells with functional GJ. PNS (50-200 µg/mL) significantly enhanced cisplatin cytotoxicity, but this effect required functional gap junctions between the cells. Exposure of the cells to PNS (50-200 µg/mL) for 4 h leads to a significant enhance in dye coupling of GJ in a dose-dependent manner. These results suggest that PNS increases the cytotoxicity of cisplatin through enhancement of GJ activity.
三七总皂苷(PNS)已被证明具有抗肿瘤活性,并增强某些癌症化疗药物的细胞毒性,但这些作用的机制尚不清楚。本研究探讨了 PNS 对顺铂细胞毒性的影响,以及 PNS 通过调节转染细胞系中的缝隙连接(GJ)功能与这种作用之间的关系。在 GJ 存在的情况下,顺铂(0.25-1μg/mL)的细胞毒性增加。间隙连接抑制剂或连接蛋白(Cx)表达的阻断均可降低顺铂的细胞毒性。增加 GJ 功能增强了顺铂的细胞毒性,但仅在具有功能 GJ 的细胞中。PNS(50-200μg/mL)显著增强了顺铂的细胞毒性,但这种作用需要细胞之间功能性的缝隙连接。细胞暴露于 PNS(50-200μg/mL)4 小时后,以剂量依赖的方式导致 GJ 染料偶联显著增强。这些结果表明,PNS 通过增强 GJ 活性增加顺铂的细胞毒性。