Miglietta Antonella, Bozzo Francesca, Gabriel Ludovica, Bocca Claudia
Department of Experimental Medicine and Oncology, University of Torino, Corso Raffaello 30, 10125 Torino, Italy.
Chem Biol Interact. 2004 Oct 15;149(2-3):165-73. doi: 10.1016/j.cbi.2004.07.005.
Parthenolide is an active sesquiterpene lactone present in a variety of medicinal herbs, well known as anti-inflammatory drug. It has recently been proposed as a chemotherapeutic drug, but the pharmacological pathways of its action have not yet been fully elucidated. Firstly, we explored whether the anticancer properties of parthenolide may be related to a tubulin/microtubule-interfering activity. We additionally compared bioactivities of parthenolide with those checked after combined treatments with paclitaxel in human breast cancer MCF-7 cells. Parthenolide exerted in vitro stimulatory activity on tubulin assembly, by inducing the formation of well-organized microtubule polymers. Light microscopy detections showed that parthenolide-induced alterations of either microtubule network and nuclear morphology happened only after combined exposures to paclitaxel. In addition, the growth of MCF-7 cells was significantly inhibited by parthenolide, which enhanced paclitaxel effectiveness. In conclusion, the antimicrotubular and antiproliferative effects of parthenolide, well known microtubule-stabilizing anticancer agent, may influence paclitaxel activity. The tubulin/microtubule system may represent a novel molecular target for parthenolide, to be utilized in developing new combinational anticancer strategies.
小白菊内酯是一种存在于多种药草中的活性倍半萜内酯,是一种著名的抗炎药物。最近它被提议作为一种化疗药物,但其作用的药理学途径尚未完全阐明。首先,我们探究了小白菊内酯的抗癌特性是否可能与微管蛋白/微管干扰活性有关。我们还比较了小白菊内酯与人乳腺癌MCF-7细胞中紫杉醇联合处理后的生物活性。小白菊内酯通过诱导形成组织良好的微管聚合物,对微管蛋白组装发挥体外刺激活性。光学显微镜检测表明,只有在与紫杉醇联合暴露后,小白菊内酯诱导的微管网络和核形态改变才会发生。此外,小白菊内酯显著抑制了MCF-7细胞的生长,增强了紫杉醇的疗效。总之,著名的微管稳定抗癌剂小白菊内酯的抗微管和抗增殖作用可能会影响紫杉醇的活性。微管蛋白/微管系统可能是小白菊内酯的一个新的分子靶点,可用于开发新的联合抗癌策略。