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机构地区:[1]福建医科大学附属第一医院药学部,福州350005 [2]福建医科大学药学院药理系,福州350004
出 处:《中国药学杂志》2010年第15期1149-1153,共5页Chinese Pharmaceutical Journal
基 金:福建省青年科技人才创新基金资助项目(2002J045);福建省卫生厅青年基金资助项目(2008-1-31)
摘 要:目的比较α-双炔失碳酯(α-Ano)对激素依赖型与非激素依赖型前列腺癌体内外作用强弱的差别。方法应用SRB细胞染色法检测α-Ano对人前列腺癌激素依赖型细胞LNCaP、RV1、L1A和非激素依赖细胞DU145、PC-3生长的影响;裸鼠皮下接种人前列腺癌细胞RV1、PC-3,构建实体瘤模型,成瘤后分组并灌胃给药,观察测量肿瘤体积及质量变化,计算肿瘤增长百分率和抑瘤率,比较α-Ano对激素依赖型和非激素依赖型人前列腺癌裸鼠皮下移植瘤生长的抑制作用。结果α-Ano作用后,LNCaP、RV1和L1A细胞生存率均低于DU145、PC-3细胞;α-Ano高低剂量组均对裸鼠皮下RV1细胞移植瘤具有较强的抑制生长作用,而对PC-3细胞移植瘤作用较弱,仅高剂量组有一定抑制作用。结论α-Ano对激素依赖型前列腺癌的抑制作用强于非激素依赖型前列腺癌。OBJECTIVE To investigate the in vitro and in vivo effects of α-anordrin(α-Ano)on androgen-dependent and androgen-independent human prostate cancer,and compare the effect difference between them.METHODS SRB staining was applied to investigate the suppression effect of α-Ano on androgen-dependent human prostate cancer cells(LNCaP,RV1 and L1A) and androgen-independent cells (DU145 and PC-3).Athymic nude mice were subcutaneously inoculated with cells suspension to construct transplantation tumor model.After intragastric administration with α-Ano,the volume of tumor was measured and the suppression rate of the drug to the proliferation of solid tumor was calculated.RESULTS After being treated by α-Ano,the survival of LNCaP,RV1 and L1A were lower than that of DU145 and PC-3.α-Ano significantly inhibited the RV-1 xenografts tumor growth at high and low concentration,but retarded PC-3 xenografts tumor growth tenderly.α-Ano exhibited inhibition effect on PC-3 xenografts tumor at high concertration,whereas no effect at low concentration.CONCLUSION The suppression effects of α-Ano on androgen-dependent human prostate cancer is stronger than that androgen-independent cancer.
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