Tomita Yoko, Smith Eric, Palethorpe Helen M, Nakhjavani Maryam, Yeo Kenny K L, Townsend Amanda R, Price Timothy J, Yool Andrea J, Hardingham Jennifer E
Solid Tumour Group, Basil Hetzel Institute for Translational Health Research, The Queen Elizabeth Hospital, Woodville South, SA 5011, Australia.
Adelaide Medical School, University of Adelaide, Adelaide, SA 5005, Australia.
Pharmaceuticals (Basel). 2021 May 6;14(5):436. doi: 10.3390/ph14050436.
We previously showed how triterpene saponin bacopaside (bac) II, purified from the medicinal herb , induced cell death in colorectal cancer cell lines and reduced endothelial cell migration and tube formation, and further demonstrated a synergistic effect of a combination of bac I and bac II on the inhibition of breast cancer cell line growth. Here, we assessed the effects of bac I and II on the colorectal cancer HT-29 cell line, and mouse (2H-11) and human umbilical vein endothelial cell (HUVEC) lines, measuring outcomes including cell viability, proliferation, migration, tube formation, apoptosis, cytosolic Ca levels and plasma membrane integrity. Combined bac I and II, each applied at concentrations below IC values, caused a synergistic reduction of the viability and proliferation of HT-29 and endothelial cells, and impaired the migration of HT-29 and tube formation of endothelial cells. A significant enhancement of apoptosis was induced only in HUVEC, although an increase in cytosolic Ca was detected in all three cell lines. Plasma membrane integrity was compromised in 2H-11 and HUVEC, as determined by an increase in propidium iodide staining, which was preceded by Ca flux. These in vitro findings support further research into the mechanisms of action of the combined compounds for potential clinical use.
我们之前展示了从药草中纯化得到的三萜皂苷胡黄连苷(bac)II如何诱导结肠癌细胞系发生细胞死亡,并减少内皮细胞迁移和血管生成,还进一步证明了胡黄连苷I和胡黄连苷II联合使用对抑制乳腺癌细胞系生长具有协同作用。在此,我们评估了胡黄连苷I和II对结肠癌细胞系HT - 29、小鼠(2H - 11)和人脐静脉内皮细胞(HUVEC)系的影响,检测指标包括细胞活力、增殖、迁移、血管生成、凋亡、胞质钙水平和质膜完整性。联合使用浓度低于半数抑制浓度(IC值)的胡黄连苷I和II会协同降低HT - 29细胞和内皮细胞的活力与增殖,并损害HT - 29细胞的迁移以及内皮细胞的血管生成。仅在HUVEC中诱导了凋亡的显著增强,尽管在所有三种细胞系中均检测到胞质钙增加。通过碘化丙啶染色增加确定,2H - 11和HUVEC中的质膜完整性受到损害,且这一现象发生在钙通量之后。这些体外研究结果支持进一步研究联合化合物的作用机制,以用于潜在的临床应用。