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柚皮素和紫杉醇协同诱导癌细胞凋亡。

Synergistic effects of apigenin and paclitaxel on apoptosis of cancer cells.

机构信息

Jiangsu Province Key Laboratory for Molecular and Medicine Biotechnology, College of Life Science, Nanjing Normal University, Nanjing, Jiangsu, People's Republic of China.

出版信息

PLoS One. 2011;6(12):e29169. doi: 10.1371/journal.pone.0029169. Epub 2011 Dec 21.

Abstract

BACKGROUND

It was well known that the clinical use of chemotherapeutic drugs is restricted by severe adverse reactions and drug resistances. Thus it is necessary to figure out a strategy to increase the specific anti-tumor efficiency of chemotherapeutic drugs. Apigenin, a kind of flavonoids, has been reported to possess anticancer activities with very low cytotoxicity to normal tissue.

METHODOLOGY/PRINCIPAL FINDINGS: Our results from cell viability assay, western-blots and TdT-mediated dUTP-biotin nick end labeling (TUNEL) assay demonstrated the synergistic pro-apoptotic effects of a low dose of apigenin and paclitaxel in human cancer cell lines. To analyze the underlying mechanism, we examined reactive oxygen species (ROS) staining after cells were treated with a combination of apigenin and paclitaxel, or each of them alone. Data from flow-cytometry showed that superoxides but not reduction of peroxides accumulated in HeLa cells treated with apigenin or a combination of apigenin and paclitaxel. Apigenin and paclitaxel-induced HeLa cell apoptosis was related to the level of ROS in cells. We further evaluated activity and protein level of superoxide dismutase (SOD). Apigenin significantly inhibited SOD activity but did not alter the SOD protein level suggesting that apigenin promoted ROS accumulation through suppressing enzyme activity of SOD. Addition of Zn(2+), Cu(2+) and Mn(2+) to cell lysates inhibited apigenin's effects on SOD activity. At the same time, data from caspase-2 over-expression and knocked-down experiments demonstrated that caspase-2 participated in apigenin and paclitaxel-induced HeLa cell apoptosis.

CONCLUSIONS/SIGNIFICANCE: Taken together, our study demonstrated that apigenin can sensitize cancer cells to paclitaxel induced apoptosis through suppressing SOD activity, which then led to accumulation of ROS and cleavage of caspase-2, suggesting that the combined use of apigenin and paclitaxel was an effective way to decrease the dose of paclitaxel taken.

摘要

背景

众所周知,化疗药物的临床应用受到严重不良反应和耐药性的限制。因此,有必要找到一种策略来提高化疗药物的特异性抗肿瘤效率。芹菜素是一种黄酮类化合物,已被报道具有抗癌活性,对正常组织的细胞毒性非常低。

方法/主要发现:我们通过细胞活力测定、western blot 和 TdT 介导的 dUTP-生物素切口末端标记(TUNEL)测定,证明了低剂量芹菜素与紫杉醇联合应用对人癌细胞系具有协同促凋亡作用。为了分析潜在的机制,我们在单独用芹菜素或芹菜素与紫杉醇联合处理细胞后,检查了活性氧(ROS)染色。流式细胞术数据显示,在用芹菜素或芹菜素与紫杉醇联合处理的 HeLa 细胞中,超氧化物而不是过氧化物减少,细胞内 ROS 积累。芹菜素和紫杉醇诱导的 HeLa 细胞凋亡与细胞内 ROS 水平有关。我们进一步评估了超氧化物歧化酶(SOD)的活性和蛋白水平。芹菜素显著抑制 SOD 活性,但不改变 SOD 蛋白水平,表明芹菜素通过抑制 SOD 的酶活性促进 ROS 积累。向细胞裂解物中添加 Zn(2+)、Cu(2+)和 Mn(2+)抑制了芹菜素对 SOD 活性的影响。同时,caspase-2 过表达和敲低实验的数据表明,caspase-2 参与了芹菜素和紫杉醇诱导的 HeLa 细胞凋亡。

结论/意义:综上所述,我们的研究表明,芹菜素可以通过抑制 SOD 活性使癌细胞对紫杉醇诱导的凋亡敏感,从而导致 ROS 积累和 caspase-2 的切割,这表明联合使用芹菜素和紫杉醇是减少紫杉醇剂量的有效方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/988d/3244456/6ccc676e6419/pone.0029169.g001.jpg

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