Gurfinkel Debbie M, Chow Sue, Hurren Rose, Gronda Marcela, Henderson Clare, Berube Christina, Hedley David W, Schimmer Aaron D
The Princess Margaret Hospital and the Ontario Cancer Institute, Rm 9-516, 610 University Ave, M5G 2M9, Toronto, ON, Canada.
Apoptosis. 2006 Sep;11(9):1463-71. doi: 10.1007/s10495-006-9086-z.
Triterpenoids are a novel class of compounds being investigated as potential therapeutic agents for the treatment of prostate cancer and other malignancies. Asiatic acid (AA) is a member of the ursane family of triterpenoids and has anticancer activity, but its mechanism of action is not completely understood. To investigate its mechanism of action, PPC-1 prostate cancer cells were treated with AA at increasing concentrations and times. AA induced rapid caspase-dependent and independent cell death that peaked within 8 h of treatment. AA-induced death was associated with early activation of caspases 2, 3, and 8, but not caspase 9. Within 2.5 h of treatment, release of calcium from intracellular stores and dilatation of the endoplasmic reticulum was observed. Thus, disruption of the endoplasmic reticulum and alterations in calcium homeostasis are early events in AA-induced death.
三萜类化合物是一类新型化合物,正作为治疗前列腺癌和其他恶性肿瘤的潜在治疗剂进行研究。积雪草苷(AA)是乌苏烷类三萜化合物家族的成员,具有抗癌活性,但其作用机制尚未完全了解。为了研究其作用机制,用不同浓度和时间的AA处理PPC-1前列腺癌细胞。AA诱导快速的半胱天冬酶依赖性和非依赖性细胞死亡,在处理后8小时达到峰值。AA诱导的细胞死亡与半胱天冬酶2、3和8的早期激活有关,但与半胱天冬酶9无关。在处理后2.5小时内,观察到细胞内钙库释放钙以及内质网扩张。因此,内质网的破坏和钙稳态的改变是AA诱导细胞死亡的早期事件。