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Activity of mevalonate pathway inhibitors against breast and ovarian cancers in the ATP-based tumour chemosensitivity assay

机译:甲羟戊酸途径抑制剂在基于ATP的肿瘤化学敏感性测定中对乳腺癌和卵巢癌的活性

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摘要

Previous data suggest that lipophilic statins such as fluvastatin and N-bisphosphonates such as zoledronic acid, both inhibitors of the mevalonate metabolic pathway, have anti-cancer effects in vitro and in patients. We have examined the effect of fluvastatin alone and in combination with zoledronic acid in the ATP-based tumour chemosensitivity assay (ATP-TCA) for effects on breast and ovarian cancer tumour-derived cells. Both zoledronic acid and fluvastatin showed activity in the ATP-TCA against breast and ovarian cancer, though fluvastatin alone was less active, particularly against breast cancer. The combination of zoledronic acid and fluvastatin was more active than either single agent in the ATP-TCA with some synergy against breast and ovarian cancer tumour-derived cells. Sequential drug experiments showed that pre-treatment of ovarian tumour cells with fluvastatin resulted in decreased sensitivity to zoledronic acid. Addition of mevalonate pathway components with zoledronic acid with or without fluvastatin showed little effect, while mevalonate did reduced inhibition due to fluvastatin. These data suggest that the combination of zoledronic acid and fluvastatin may have activity against breast and ovarian cancer based on direct anti-cancer cell effects. A clinical trial to test this is in preparation.
机译:先前的数据表明,亲脂性他汀类药物(例如氟伐他汀)和N-双膦酸酯类(例如唑来膦酸)都是甲羟戊酸代谢途径的抑制剂,在体外和患者中均具有抗癌作用。我们已经在基于ATP的肿瘤化学敏感性测定(ATP-TCA)中检查了氟伐他汀单独或与唑来膦酸联用对乳腺癌和卵巢癌肿瘤衍生细胞的作用。唑来膦酸和氟伐他汀都在ATP-TCA中显示出抗乳腺癌和卵巢癌的活性,尽管氟伐他汀本身的活性较低,尤其是抗乳腺癌。唑来膦酸和氟伐他汀的组合比ATP-TCA中的任何一种单药更具活性,并且对乳腺癌和卵巢癌肿瘤衍生细胞具有一定的协同作用。顺序药物实验表明,用氟伐他汀预处理卵巢肿瘤细胞会降低对唑来膦酸的敏感性。甲氧戊酸途径成分与唑来膦酸加或不加氟伐他汀的效果均不明显,而甲羟戊酸的确抑制了氟伐他汀的抑制作用。这些数据表明,基于直接的抗癌细胞作用,唑来膦酸和氟伐他汀的组合可能具有抗乳腺癌和卵巢癌的活性。对此进行临床试验的准备中。

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