Kanje M, Deinum J, Wallin M, Ekström P, Edström A, Hartley-Asp B
Cancer Res. 1985 May;45(5):2234-9.
Estramustine phosphate (0.01 to 0.5 mM), an estradiol mustard derivative used in the therapy of prostatic carcinoma, inhibited the assembly of brain microtubules proteins in vitro and disassembled preformed microtubules. In the presence of estramustine phosphate, the minimum microtubule-protein concentration sufficient for the assembly of microtubules was increased. Low concentrations of taxol (20 microM) completely reversed the inhibition of assembly by estramustine phosphate. The effects were specific to estramustine phosphate since neither estradiol 17 beta-phosphate, the hormonal moiety of the drug, nor nornitrogen mustard, the alkylating moiety, had any effect on assembly. Estramustine phosphate (0.1 to 0.5 mM) was also found to reversibly inhibit fast axonal transport in the frog sciatic nerve. The nerve content of adenosine triphosphate, adenosine diphosphate, and adenosine monophosphate was not significantly affected by estramustine phosphate. Our results suggest that the cytotoxic action of estramustine phosphate could be dependent partially on an interaction with microtubules, probably via the microtubule-associated proteins.
磷酸雌莫司汀(0.01至0.5 mM)是一种用于前列腺癌治疗的雌二醇氮芥衍生物,它在体外抑制脑微管蛋白的组装,并使预先形成的微管解聚。在磷酸雌莫司汀存在的情况下,足以组装微管的最低微管蛋白浓度增加。低浓度的紫杉醇(20 microM)完全逆转了磷酸雌莫司汀对组装的抑制作用。这些作用对磷酸雌莫司汀具有特异性,因为该药物的激素部分17β-磷酸雌二醇和烷基化部分去甲氮芥对组装均无任何影响。还发现磷酸雌莫司汀(0.1至0.5 mM)可逆地抑制青蛙坐骨神经中的快速轴突运输。磷酸雌莫司汀对三磷酸腺苷、二磷酸腺苷和一磷酸腺苷的神经含量没有显著影响。我们的结果表明,磷酸雌莫司汀的细胞毒性作用可能部分取决于与微管的相互作用,可能是通过微管相关蛋白实现的。