Steinman Richard A, Brufsky Adam M, Oesterreich Steffi
Breast Cancer Res. 2012 Sep 21;14(5):213. doi: 10.1186/bcr3223.
Zoledronic acid (ZA) is an imidazole-containing bisphosphonate that has been extensively studied as an osteoclast inhibitor. ZA decreases bone turnover and has been effective in limiting osteolysis in metastatic cancers, including breast cancer. Recent clinical trials that demonstrated enhancement of disease-free survival by bisphosphonates have prompted interest in bisphosphonates as anti-cancer agents. ZA, for example, increased disease-free survival in postmenopausal and in premenopausal, hormone-suppressed breast cancer patients. Intriguingly, however, there was a lack of an anti-cancer effect of ZA in premenopausal women without ovarian suppression. These observations have prompted the conjecture that anti-cancer effects of ZA are limited to estrogen-poor environments. This review explores possible mechanisms compatible with differences in ZA activity in premenopausal women compared with postmenopausal (or hormone-suppressed) women.
唑来膦酸(ZA)是一种含咪唑的双膦酸盐,作为破骨细胞抑制剂已得到广泛研究。ZA可降低骨转换,并已有效限制转移性癌症(包括乳腺癌)中的骨溶解。近期的临床试验表明双膦酸盐可提高无病生存率,这引发了人们对双膦酸盐作为抗癌药物的兴趣。例如,ZA提高了绝经后以及绝经前接受激素抑制治疗的乳腺癌患者的无病生存率。然而,有趣的是,在未接受卵巢抑制的绝经前女性中,ZA缺乏抗癌效果。这些观察结果促使人们推测,ZA的抗癌作用仅限于雌激素水平较低的环境。本综述探讨了与绝经前女性相比绝经后(或接受激素抑制治疗)女性中ZA活性差异相符的可能机制。