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氟维司群与多种细胞毒药物(阿霉素、紫杉醇、多西他赛、长春瑞滨和 5-氟尿嘧啶)联合治疗具有协同作用,可用于治疗雌激素受体阳性乳腺癌。

Combination treatment with fulvestrant and various cytotoxic agents (doxorubicin, paclitaxel, docetaxel, vinorelbine, and 5-fluorouracil) has a synergistic effect in estrogen receptor-positive breast cancer.

机构信息

Department of Cancer and Thoracic Surgery, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, Okayama, Japan.

出版信息

Cancer Sci. 2011 Nov;102(11):2038-42. doi: 10.1111/j.1349-7006.2011.02050.x. Epub 2011 Sep 1.

Abstract

Patients with estrogen receptor (ER)-positive breast cancers have a better prognosis than those with ER-negative breast cancers, but often have low sensitivity to chemotherapy and a limited survival benefit. We have previously shown a combination effect of taxanes and fulvestrant and suggested that this treatment may be useful for ER-positive breast cancer. In this study, we evaluated the effects of combinations of hormone drugs and chemotherapeutic agents. In vitro, the effects of combinations of five chemotherapeutic agents (doxorubicin, paclitaxel, docetaxel, vinorelbine, and 5-fluorouracil) and three hormone drugs (fulvestrant, tamoxifen, and 4-hydroxytamoxifen) were examined in ER-positive breast cancer cell lines using CalcuSyn software. Changes in chemoresistant factors such as Bcl2, multidrug resistance-associated protein 1, and microtubule-associated protein tau were also examined after exposure of the cells to hormone drugs. In vivo, tumor sizes in mice were evaluated after treatment with docetaxel or doxorubicin alone, fulvestrant alone, and combinations of these agents. Combination treatment with fulvestrant and all five chemotherapeutic agents in vitro showed synergistic effects. In contrast, tamoxifen showed an antagonistic effect with all the chemotherapeutic agents. 4-Hydroxytamoxifen showed an antagonistic effect with doxorubicin and 5-fluorouracil, but a synergistic effect with taxanes and vinorelbine. Regarding chemoresistant factors, Bcl2 and microtubule-associated protein tau were downregulated by fulvestrant. In vivo, a combination of fulvestrant and docetaxel had a synergistic effect on tumor growth, but fulvestrant and doxorubicin did not show this effect. In conclusion, fulvestrant showed good compatibility with all the evaluated chemotherapeutic agents, and especially with docetaxel, in vitro and in vivo.

摘要

患有雌激素受体(ER)阳性乳腺癌的患者比 ER 阴性乳腺癌患者的预后更好,但通常对化疗的敏感性较低,生存获益有限。我们之前已经证明了紫杉烷和氟维司群的联合作用,并表明这种治疗可能对 ER 阳性乳腺癌有用。在这项研究中,我们评估了激素药物和化疗药物联合的效果。在体外,使用 CalcuSyn 软件研究了五种化疗药物(阿霉素、紫杉醇、多西紫杉醇、长春瑞滨和 5-氟尿嘧啶)和三种激素药物(氟维司群、他莫昔芬和 4-羟基他莫昔芬)在 ER 阳性乳腺癌细胞系中的联合作用。还检查了细胞暴露于激素药物后,耐药因素(如 Bcl2、多药耐药相关蛋白 1 和微管相关蛋白 tau)的变化。在体内,单独用多西紫杉醇或阿霉素、氟维司群以及这些药物的组合治疗后,评估了小鼠肿瘤的大小。体外联合治疗氟维司群和所有五种化疗药物显示出协同作用。相比之下,他莫昔芬与所有化疗药物均显示拮抗作用。4-羟基他莫昔芬与阿霉素和 5-氟尿嘧啶显示拮抗作用,但与紫杉烷和长春瑞滨显示协同作用。关于耐药因素,氟维司群下调了 Bcl2 和微管相关蛋白 tau。在体内,氟维司群和多西紫杉醇的组合对肿瘤生长具有协同作用,但氟维司群和阿霉素没有这种作用。总之,氟维司群在体外和体内与所有评估的化疗药物均具有良好的兼容性,尤其是与多西紫杉醇。

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