Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA; Laboratory of Biochemistry and Molecular Biology, Faculty of Sciences of Bizerte, University of Carthage, Tunisia.
Department of Experimental Therapeutics, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Biomed Pharmacother. 2017 Nov;95:1876-1885. doi: 10.1016/j.biopha.2017.09.115. Epub 2017 Oct 6.
Teucrium alopecurus is an endemic plant limited to southern Tunisia. In the present study, the chemical composition, anticancer and nuclear factor-κB (NF-κB) inhibitory effects of Teucrium alopecurus leaf essential oil was investigated. The analysis of Teucrium alopecurus (TA-1) with Gas Chromatography-Mass Spectrometry (GC/MS) showed that α-Bisabolol, (+)-epi-Bicyclosesquiphellandrene and α-Cadinol, were found in relatively high amounts (16.16%, 15.40% and 8.52%, respectively). Cell viability was determined by 3-(4-5-dimethylthiazol-2-yl) 2-5-diphenyl-tetrazolium (MTT) assay. Cell cycle and apoptosis assay were determined by flow cytometry. TA-1 functions as an anticancer agent by triggering apoptosis potentiated by chemotherapeutic agents and TNF in human myeloid leukemia cells (KBM5) through a mechanism involving poly(ADP-ribose) polymerase (PARP) cleavage and initiator and effector caspases activation. Moreover, electrophoretic mobility shift assay (EMSA) revealed that TA-1 downregulated nuclear localization of NF-κB and its phosphorylation induced by TNF-α and this, allows the suppression of the degradation and phosphorylation of IκB and the inhibition of the phosphorylation of p65 phosphorylation and the p50-p65 heterodimer nuclear translocation, causing attenuation of NF-κB-regulated antiapoptotic (Survivin, Bcl-2, c-IAP1/2, Bcl-xL, Mcl-1, and cFLIP), invasion (ICAM1), metasatsis (MMP-9), and angiogenesis (VEGF) gene expression in KBM5; and finally reporter gene expression. Furthermore, treatment with essential oil and TNF-α suppressed the NF-κB DNA binding activity. Finally, the activation of nuclear factor-κB induced by different plasmids (TNFR1, TRADD, TRAF2, NIK, TAK1/TAB1, and IKKβ) was inhibited following treatment with TA-1. Overall, TA-1 inhibits NF-κB activation and further growth and proliferation of cancer cells.
獐牙菜属是一种局限于突尼斯南部的特有植物。在本研究中,研究了獐牙菜属叶精油的化学成分、抗癌作用和核因子-κB(NF-κB)抑制作用。用气相色谱-质谱联用仪(GC/MS)对獐牙菜(TA-1)进行分析,发现 α- 毕枯醇、(+)-表双环倍半萜烯和 α- 杜松醇的含量相对较高(分别为 16.16%、15.40%和 8.52%)。通过 3-(4-5-二甲基噻唑-2-基)-2,5-二苯基四氮唑(MTT)测定法测定细胞活力。通过流式细胞术测定细胞周期和细胞凋亡。TA-1 通过触发化疗药物和 TNF 在人髓样白血病细胞(KBM5)中诱导的细胞凋亡,作为一种抗癌剂发挥作用,其机制涉及聚(ADP-核糖)聚合酶(PARP)切割以及起始和效应半胱天冬酶的激活。此外,电泳迁移率变动分析(EMSA)显示 TA-1 下调了 TNF-α诱导的 NF-κB 的核定位及其磷酸化,从而抑制了 IκB 的降解和磷酸化以及 p65 磷酸化和 p50-p65 异二聚体核易位,并导致 NF-κB 调节的抗凋亡(Survivin、Bcl-2、c-IAP1/2、Bcl-xL、Mcl-1 和 cFLIP)、侵袭(ICAM1)、转移(MMP-9)和血管生成(VEGF)基因表达在 KBM5 中的衰减;最后报告基因表达。此外,用精油和 TNF-α处理可抑制 NF-κB 的 DNA 结合活性。最后,TA-1 处理抑制了不同质粒(TNFR1、TRADD、TRAF2、NIK、TAK1/TAB1 和 IKKβ)诱导的核因子-κB 的激活。总的来说,TA-1 抑制 NF-κB 的激活,并进一步抑制癌细胞的生长和增殖。