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Epothilones: tubulin polymerization as a novel target for prostate cancer therapy.

机译:上皮激素:微管蛋白聚合作为前列腺癌治疗的新靶标。

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Microtubules are vital and dynamic cellular organelles and many agents have been developed that target them. The cytotoxic effects of taxanes and epothilones are mediated by stabilization of microtubule dynamics. Taxanes are one of the most effective cytotoxic agents, and have a broad spectrum of antitumor activity. However, their efficacy is limited by the development of resistance to these effects. Epothilones have a similar mechanism of action to taxanes, but a decreased propensity for drug resistance. Epothilones are macrolides, and have in vitro and in vivo activity in taxane-resistant or taxane-insensitive human cancer cell lines. Several epothilones are in clinical development: ixabepilone, patupilone, BMS-310705, KOS-862, KOS-1584, and ZK-EPO. Multiple dosing schedules of ixabepilone and patupilone have been studied. The toxicity profiles of epothilones are quite diverse and depend on the compound and the administration schedule. The epothilones have demonstrated a wide range of clinical activity, including important antitumor effects, in advanced prostate cancer. Epothilones are particularly useful in patients with prostate cancer who have previously been treated with taxanes or who have taxane-refractory tumors. In the setting of castrate metastatic prostate cancer, ixabepilone and patupilone showed encouraging clinical activity in the phase II setting and further studies are needed to determine if they provide additional clinical benefit to patients with advanced disease.
机译:微管是至关重要的和动态的细胞器,并且已经开发出许多靶向它们的药剂。紫杉烷和埃博霉素的细胞毒性作用是通过微管动力学的稳定来介导的。紫杉烷类是最有效的细胞毒性剂之一,并具有广泛的抗肿瘤活性。然而,它们的功效受到对这些作用的抗性发展的限制。依匹洛酮的作用机理与紫杉烷类相似,但耐药性降低。环氧噻酮是大环内酯类,并且在抗紫杉烷类或对紫杉烷类不敏感的人类癌细胞系中具有体外和体内活性。几种埃博霉素正在临床开发中:依沙贝比隆,帕布匹隆,BMS-310705,KOS-862,KOS-1584和ZK-EPO。 ixabepilone和patupilone的多种给药方案已被研究。埃博霉素的毒性特征非常多样,取决于化合物和给药方案。埃博霉素在晚期前列腺癌中已显示出广泛的临床活性,包括重要的抗肿瘤作用。依匹洛酮在以前用紫杉烷类药物治疗或患有紫杉烷类难治性肿瘤的前列腺癌患者中特别有用。在去势转移性前列腺癌的背景下,依沙贝比隆和帕普匹隆在II期阶段显示出令人鼓舞的临床活性,需要进一步研究以确定它们是否为晚期疾病患者提供更多的临床益处。

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