Volatile oil of Teucrium alopecurus sensitizes colon cancer cells to TRAIL-induced cell death.

Fatma Guesmi, Sahdeo Prasad, Wiem Tahri, Imen Dridi, Manel Ben Ali, Amor Hedfi, Ismail A Ismail, Ahmed Landoulsi
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引用次数: 1

Abstract

TNF-related apoptosis-inducing ligand (TRAIL/Apo2L), a member of cytokine family, is known to selectively induce apoptosis in cancer cells. However, developing resistance to TRAIL is a major obstacle in cancer therapy. In this study, the in vitro effect of Teucrium alopecurus (TA) essential oil on inhibition of cancer cell growth and enhancing TRAIL-induced apoptosis were investigated in colon cancer cells. Untreated tumor cell lines are used as controls. TA induced cell death and increased the anticancer effects of TRAIL as observed by cell toxicity, live/dead assay, cleavage of caspases and PARP. Furthermore, the mechanism of anticancer potentiating effect of TA was found to be linked with the upregulation of death receptors (DRs) and reduced expression of TRAIL decoy receptors (DcRs). TA also down-regulated antiapoptotic proteins and induced p53 in colon cancer cells. In addition, we observed upregulation of MAPK signalling pathway (p38 kinase, JNK, ERK) and increased expression of C/EBP homologous transcription factor (CHOP) and specificity protein 1 (SP1) by TA. These findings demonstrate the potent anticancer effect of bioactive constituents of Teucrium alopecurus essential oil.

白头草挥发油使结肠癌细胞对trail诱导的细胞死亡敏感。
tnf相关凋亡诱导配体(TRAIL/Apo2L)是细胞因子家族的一员,可选择性诱导癌细胞凋亡。然而,对TRAIL产生耐药性是癌症治疗的主要障碍。本实验以结肠癌细胞为实验对象,研究了白头草(Teucrium alopecurus, TA)精油对肿瘤细胞生长的抑制作用以及对trail诱导的细胞凋亡的促进作用。未治疗的肿瘤细胞系作为对照。通过细胞毒性、活/死实验、半胱天冬酶和PARP的裂解观察到,TA诱导细胞死亡,增加TRAIL的抗癌作用。此外,发现TA的抗癌增强作用机制与上调死亡受体(dr)和降低TRAIL诱饵受体(dcr)的表达有关。TA还能下调结肠癌细胞的抗凋亡蛋白并诱导p53。此外,我们观察到TA上调了MAPK信号通路(p38激酶、JNK、ERK),增加了C/EBP同源转录因子(CHOP)和特异性蛋白1 (SP1)的表达。这些发现证明了白头草精油的生物活性成分具有较强的抗癌作用。
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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