非小细胞肺癌体外多药耐药(阿魏酸和紫杉醇)的生化评价

J.P. Jose Merlin , B. Venkadesh , R. Hussain , S.S. Rajan
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引用次数: 5

摘要

阿魏酸(FA)是一种具有较强抗癌作用的酚类植物营养素。然而,由于肿瘤部位的生物利用度差,其在癌症中的突出应用受到限制。紫杉醇(PTX)是一种半合成药物,用于癌症治疗。本研究旨在探讨FA和PTX的多药耐药情况。FA + PTX的抗癌潜力大于FA和PTX单独治疗。此外,与单独使用FA和PTX相比,FA + PTX在NCI-H460细胞中表现出增加的TBARS,过氧化氢酶和SOD,改变的GSH和GPx。我们的研究结果表明,FA + PTX在癌细胞中表现出比FA和PTX单独治疗更强的抗癌特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biochemical estimations of multidrug resistance (ferulic acid and paclitaxel) in non-small cells lung carcinoma cells in vitro

Ferulic acid (FA) is a phenolic phytonutrient, which possesses strong anticancer effect. However, its prominent application in cancer is limited due to poor bioavailability at the tumor site. Paclitaxel (PTX) is a semi synthetic drug which is used for cancer treatment. The aim of the study was to investigate the multidrug resistance of FA and PTX. It was noticed that anticancer potential of FA + PTX was greater than that of FA and PTX treatment alone. Further, FA + PTX exhibits increased TBARS, Catalase and SOD, altered GSH and GPx in NCI-H460 cells when compared to bulk FA and PTX treatment alone. Our results indicate that FA + PTX demonstrated increased anticancer property in cancer cells than FA and PTX treatment alone.

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