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[雌氮芥(雌二醇氮芥复合物)——雌氮芥结合蛋白及其特异性]

[Estracyt (estradiol-nitrogen mustard complex)--estramustine binding protein and its specificity].

作者信息

Yamanaka H, Imai K, Suzuki T, Yuasa H, Takahashi E

出版信息

Gan To Kagaku Ryoho. 1984 Oct;11(10):2106-14.

PMID:6486830
Abstract

Estracyt (estramustine phosphate) is a nitrogen mustard derivative of estradiol-17 beta which is rapidly dephosphorylated to yield estramustine. Estramustine is metabolized to estromustine mainly in the liver. Both estramustine and estromustine are retained in rat prostate with a high degree of specificity. This retention is due to the binding of estramustine and/or estromustine to a protein called EMBP (estramustine binding protein). When estimated by HPLC, the molecular weights of these estramustine binding components in rat prostate are 45,000-50,000 and 25,000-30,000, respectively. HPLC and glycerol density gradient analysis clearly demonstrated the occurrence of EMBP in a cytosol preparation from human prostatic cancer tissue. When estimated by HPLC, the molecular weights of estramustine binding components are 45,000 and 25,000 daltons, respectively. In addition, results of effectiveness of Estracyt studied under a cooperative research group in Japan, are reported in this paper. Effectiveness was evaluated at 3 months of the treatment on 121 patients with untreated prostatic cancer (Study I) and 95 patients with reactivated cancer (Study II), at 12 months of the treatment on 68 patients in Study I and 85 patients in Study II, and at 24 months on 37 patients in Study I and 23 patients in Study II. At 3 months of the treatment, Estracyt was effective in 89% of untreated prostatic cancers, and 38% of reactivated prostatic cancers. At 24 months of the treatment, this drug was effective in 65% of untreated prostatic cancers and 30% of reactivated ones. Estracyt is especially recommended as a first-choice drug for both the untreated patients with poorly differentiated adenocarcinoma and reactivated cancer.

摘要

癌腺治(磷酸雌莫司汀)是雌二醇 - 17β的氮芥衍生物,它能迅速去磷酸化生成雌莫司汀。雌莫司汀主要在肝脏代谢为雌罗司汀。雌莫司汀和雌罗司汀都以高度特异性保留在大鼠前列腺中。这种保留是由于雌莫司汀和/或雌罗司汀与一种名为EMBP(雌莫司汀结合蛋白)的蛋白质结合。通过高效液相色谱法(HPLC)估算时,大鼠前列腺中这些雌莫司汀结合成分的分子量分别为45,000 - 50,000和25,000 - 30,000。HPLC和甘油密度梯度分析清楚地证明了人前列腺癌组织的胞质溶胶制剂中存在EMBP。通过HPLC估算时,雌莫司汀结合成分的分子量分别为45,000和25,000道尔顿。此外,本文报道了日本一个合作研究小组对癌腺治有效性的研究结果。对121例未经治疗的前列腺癌患者(研究I)和95例复发癌患者(研究II)在治疗3个月时评估有效性,对研究I中的68例患者和研究II中的85例患者在治疗12个月时评估有效性,对研究I中的37例患者和研究II中的23例患者在治疗24个月时评估有效性。在治疗3个月时,癌腺治对89%的未经治疗的前列腺癌和38%的复发前列腺癌有效。在治疗24个月时,该药物对65%的未经治疗的前列腺癌和30%的复发癌有效。癌腺治特别推荐作为未分化腺癌未治疗患者和复发癌患者的首选药物。

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