首页> 外文期刊>BMC Complementary and Alternative Medicine >Apoptosis-induced effects of extract from Artemisia annua Linné by modulating PTEN/p53/PDK1/Akt/ signal pathways through PTEN/p53-independent manner in HCT116 colon cancer cells
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Apoptosis-induced effects of extract from Artemisia annua Linné by modulating PTEN/p53/PDK1/Akt/ signal pathways through PTEN/p53-independent manner in HCT116 colon cancer cells

机译:通过独立于PTEN / p53的方式调节PTEN / p53 / PDK1 / Akt /信号通路在HCT116结肠癌细胞中对青蒿提取物的凋亡诱导作用

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Background The extracts from Artemisia annua Linné (AAE) has been known to possess various functions including anti-bacterial, anti-virus and anti-oxidant effects. However, the mechanism of those effects of AAE is not well known. Pursuantly, we determined the apoptotic effects of extract of AAE in HCT116 cell. In this study, we suggested that AAE may exert cancer cell apoptosis through PTEN/PDK1/Akt/p53signal pathway and mitochondria-mediated apoptotic proteins. Methods We measured 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, lactate dehydrogenase (LDH) assay, Hoechst 33342 staining, Annexin V-PI staining, Mitopotential assay, immunofluorescence (IF) and Western blotting. Accordingly, our study showed that AAE treatment to HCT116 cells resulted in inhibition of PDK1, Akt, MDM2, Bcl-2, and pro-caspase 3 as well as activation of PTEN, p53-upregulated modulator of apoptosis (PUMA), Bax and Bak expression. Also we measured in vivo assay that xenograft model, H&E assay, TUNEL assay and IHC. Results AAE induced apoptosis via PTEN/p53/PDK1/Akt signal pathways through PTEN/p53-independent manner. AAE inhibit cell viability and increase LDH release in HCT116 colon cancer cell. Also, AAE increase apoptotic bodies, caspase ?3,7 activation and reduces mitochondria membrane potential. AAE regulates cytochrome c translocation to the cytoplasm and Bax translocation to the mitochondrial membrane in an Immunofluorescence staining and increase PTEN and p53 expression in an in vivo tumor xenograft model. To elucidate the role of the PTEN/p53/PDK1/Akt signal pathways in cancer control, we conditionally inactivated PTEN/p53/PDK1/Akt signal pathways. We used inhibitors of PTEN, p53, PDK1, Akt. In consequence, these results indicate that AAE induced apoptosis by means of a mitochondrial event through the regulation of proteins such as Bax, Bak and cytochrome c in PDK1/Akt signaling pathways via PTEM/p53-independent manner. Conclusions We confirmed the apoptotic effect of extracts of AAE by Modulating PTEN/p53/PDK1/Akt/Signal Pathways through PTEN/p53-independent pathwaysin HCT116 colon cancer cell.
机译:背景技术已知来自青蒿(AAE)的提取物具有多种功能,包括抗菌,抗病毒和抗氧化作用。但是,AAE产生这些作用的机制尚不清楚。因此,我们确定了AAE提取物对HCT116细胞的凋亡作用。在这项研究中,我们建议AAE可能通过PTEN / PDK1 / Akt / p53信号通路和线粒体介导的凋亡蛋白发挥癌细胞凋亡的作用。方法我们测量了3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物(MTT)测定,乳酸脱氢酶(LDH)测定,Hoechst 33342染色,膜联蛋白V-PI染色,线粒体测定,免疫荧光( IF)和蛋白质印迹。因此,我们的研究表明AAE对HCT116细胞的处理导致PDK1,Akt,MDM2,Bcl-2和前胱天蛋白酶3的抑制以及PTEN,p53上调的凋亡调节剂(PUMA),Bax和Bak的激活。表达。我们还测量了异种移植模型,H&E分析,TUNEL分析和IHC的体内分析。结果AAE通过PTEN / p53 / PDK1 / Akt信号通路以非PTEN / p53方式诱导细胞凋亡。 AAE抑制细胞活力并增加HCT116结肠癌细胞中LDH的释放。而且,AAE增加了凋亡小体,胱天蛋白酶α3,7活化并降低了线粒体膜电位。在免疫荧光染色中,AAE调节细胞色素c向细胞质的移位以及Bax向线粒体膜的移位,并在体内肿瘤异种移植模型中增加PTEN和p53的表达。为了阐明PTEN / p53 / PDK1 / Akt信号通路在癌症控制中的作用,我们有条件地使PTEN / p53 / PDK1 / Akt信号通路失活。我们使用了PTEN,p53,PDK1,Akt的抑制剂。因此,这些结果表明,AAE通过线粒体事件,通过不依赖PTEM / p53的方式调节PDK1 / Akt信号通路中的蛋白质(如Bax,Bak和细胞色素c)诱导细胞凋亡。结论我们通过调节PTEN / p53 / PDK1 / Akt /信号途径通过PTEN / p53非依赖性途径在HCT116结肠癌细胞中证实了AAE提取物的凋亡作用。

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