Axanova Linara, Morré D James, Morré Dorothy M
Department of Foods and Nutrition, Purdue University, 700 W. State Street, West Lafayette, IN 47907-205, USA.
Cancer Lett. 2005 Jul 8;225(1):35-40. doi: 10.1016/j.canlet.2004.11.017. Epub 2004 Dec 24.
An in vitro coculture model of prostate cancer cells (LNCaP) with human osteoblasts (hFOB) was utilized to define the efficacy of the tNOX inhibitors EGCg, capsaicin, Capsibiol-T and phenoxodiol against bone metastasis of prostate cancer alone and in combination with Taxol and cisplatin. In general, the LNCaP cells were more resistant to treatment with EGCg, capsaicin, phenoxodiol and Taxol when grown in coculture than when grown in monoculture. Only with Capsibiol-T (50 microM) was growth of LNCaP cells in coculture inhibited comparable with monoculture. Pretreatment with Capsibiol-T followed by the treatment with Taxol had an additive effect on reduction of viability of LNCaP cells in monoculture. In contrast, an antagonistic effect of cisplatin was observed following capsaicin pretreatment.
利用前列腺癌细胞(LNCaP)与人成骨细胞(hFOB)的体外共培养模型,来确定tNOX抑制剂表没食子儿没食子酸酯(EGCg)、辣椒素、Capsibiol-T和苯氧二醇单独以及与紫杉醇和顺铂联合使用时对前列腺癌骨转移的疗效。一般来说,与单培养相比,LNCaP细胞在共培养时对EGCg、辣椒素、苯氧二醇和紫杉醇治疗的耐药性更强。只有使用Capsibiol-T(50微摩尔)时,共培养中LNCaP细胞的生长抑制情况与单培养相当。先用Capsibiol-T预处理,然后用紫杉醇处理,对单培养中LNCaP细胞活力的降低有相加作用。相反,在辣椒素预处理后观察到顺铂有拮抗作用。