Enhancement of taxol-induced apoptosis by inhibition of NF-κB with ursorlic acid

Yunlong Li, D. Xing
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Abstract

Taxol is known to inhibit cell growth and triggers significant apoptosis in various cancer cells, and activation of proliferation factor NF-κB during Taxol-induced apoptosis is regarded as a main reason resulting in tumor cells resistance to Taxol. It has been found that ursorlic acid can inhibit the activation of NF-κB. In order to study whether ursorlic acid can enhance the Taxol-induced apoptosis, we use fluorescence resonance energy transfer (FRET) technique and probe SCAT3 to compare the difference of caspase-3 activation between Taxol alone and Taxol combined ursorlic acid. With laser scanning confocal microscopy, we find that ursorlic acid, a nontoxic food component, sensitizes ASTC-a-1 cells more efficiently to Taxol-induced apoptosis by advanced activation of caspase 3. The result also suggests that there would be a synergistic effect between Taxol and ursorlic acid, and the more detailed mechanism of synergistic effect needs to be clarified further, such as the correlations among NF-κB, Akt, caspase 8, which leads to the advanced activation of caspase 3 during combined treatment of Taxol and ursorlic acid. Moreover, this may be a new way to improve Taxol-dependent tumor therapy.
熊果酸抑制NF-κB增强紫杉醇诱导的细胞凋亡
紫杉醇在多种肿瘤细胞中具有抑制细胞生长和诱发显著凋亡的作用,而在紫杉醇诱导的细胞凋亡过程中活化增殖因子NF-κB被认为是导致肿瘤细胞对紫杉醇产生耐药性的主要原因。研究发现熊果酸能抑制NF-κB的活化。为了研究熊果酸是否能增强紫杉醇诱导的细胞凋亡,我们采用荧光共振能量转移(FRET)技术和探针SCAT3比较紫杉醇单独和紫杉醇联合熊果酸对caspase-3激活的差异。通过激光扫描共聚焦显微镜,我们发现熊果酸,一种无毒的食品成分,通过提前激活caspase 3,更有效地使ASTC-a-1细胞对紫杉醇诱导的凋亡敏感。该结果也提示紫杉醇与熊果酸之间存在协同作用,更详细的协同作用机制有待进一步明确,如NF-κB、Akt、caspase 8之间的相关性,从而导致紫杉醇与熊果酸联合治疗时caspase 3的提前激活。此外,这可能是改善紫杉醇依赖性肿瘤治疗的新途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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