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Phenoxodiol Treatment Alters the Subsequent Response of ENOX2 (tNOX) and Growth of HeLa Cells to Paclitaxel and Cisplatin

机译:苯氧二酚处理改变了ENOX2(tNOX)的后续反应以及HeLa细胞对紫杉醇和顺铂的生长

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Phenoxodiol is an experimental anticancer drug under development as a chemosensitizer intended to reverse multidrug resistance mechanisms in ovarian and prostate cancer cells to most standard cytotoxics. The putative molecular target of phenoxodiol is a cell-surface, tumor-specific NADH oxidase, ENOX2 (tNOX), with phenoxodiol having no apparent effect on the constitutive form of this enzyme ENOX1 (CNOX). Using ENOX2 as the target, this study was conducted to explore the temporal relationship between phenoxodiol and paclitaxel or cisplatin in achieving chemosensitization in HeLa cells which are relatively resistant to both paclitaxel and cisplatin. Sequential addition of phenoxodiol and paclitaxel or phenoxodiol and cisplatin showed greater inhibition of HeLa cell ENOX1 activity and growth compared to adding the drugs simultaneously or individually. In parallel, a similar chemosensitizing response of phenoxodiol for cisplatin was observed. ENOX1 was not affected and trans-platinum had no effect. With spent media from phenoxodiol-treated cells sensitivity was enhanced to both paclitaxel and cisplatin if the cells were first pretreated with phenoxodiol. Similar results were obtained with ENOX2-enriched preparations stripped from the surfaces of phenoxodiol-treated cells. In keeping with a speculative prion model, it seems as though the ENOX2 "remembers'' the phenoxodiol and "teaches'' other ENOX2 molecules to respond to paclitaxel and cisplatin as if phenoxodiol were still present.
机译:苯氧二酚是一种实验性抗癌药物,正在开发中,它是一种化学增敏剂,旨在使卵巢癌和前列腺癌细胞中的多药耐药机制逆转为大多数标准细胞毒素。苯氧二酚的假定分子靶标是细胞表面的肿瘤特异性NADH氧化酶ENOX2(tNOX),苯氧二酚对该酶ENOX1(CNOX)的构成形式没有明显影响。以ENOX2为靶标,进行了这项研究,以探索苯氧酚与紫杉醇或顺铂之间的时间关系,以实现对紫杉醇和顺铂均具有抗性的HeLa细胞的化学增敏作用。与同时或单独添加药物相比,依次添加苯氧索二醇和紫杉醇或苯氧索二醇和顺铂显示出对HeLa细胞ENOX1活性和生长的更大抑制作用。同时,观察到苯氧二酚对顺铂具有相似的化学致敏反应。 ENOX1不受影响,反铂无作用。如果先用苯氧二酚预处理细胞,则用苯氧二酚处理的废培养基对紫杉醇和顺铂的敏感性都会增强。从经苯氧二酚处理的细胞表面剥离的富含ENOX2的制剂获得了相似的结果。与推测性ion病毒模型保持一致,似乎ENOX2可以“记住”苯氧酚,并“教导”其他ENOX2分子对紫杉醇和顺铂起反应,就好像苯氧酚仍然存在。

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