Yang Xin-Qing, Zheng Hao, Ye Qing, Li Rui-Yu, Chen Yong
Department of Otolaryngology Head and Neck Surgery, Fujian Provincial Clinical College, Fujian Medical University, Fuzhou 350001, China.
J BUON. 2015 Nov-Dec;20(6):1518-25.
Impressed by the exceptional anticancer activity of cinnamon, the present study was conducted to elucidate the anticancer potential of essential oil of Cinnamon (EOC).
EOC was tested against various cell lines (FaDu, Detroit-562 and SCC-25) of head and neck squamous cell carcinoma (HNSCC) using MTT assay. The Hep-2 cell xenograft model was used to assess the positive bio-activity of EOC. EGFR-TK inhibitory assay was also carried out to explain the possible mechanism of action of EOC. Moreover, to rationalise the key contacts responsible for attenuating EGFR, the major component of EOC, i.e., trans-cinnamaldehyde, as identified by GC-MS analysis, was subjected to molecular docking experiments with the catalytic domain of EGFR protein model.
EOC exhibited significant anticancer activity with percent inhibition 66.12, 87.32, and 99.34%, against FaDu, Detroit-562 and SCC-25, respectively. Moreover, EOC reduced the tumor burden to 43.5% in Hep-2 cell xenograft model along with 89% inhibition of EGFR-TK activity in the EGFR-TK inhibitory assay. Docking experiments showed that trans-cinnamaldehyde was proficiently fitted into the inner grove of the active site of EGFR by making close inter-atomic contacts with the key catalytic residues Val702, Ala719, Lys721, Leu764, Thr766 and Leu820 and with inhibition constant Ki = 775.93 μM.
EOC exhibits significant anticancer activity against HNSCC cells in vitro. The mechanism underlying its anticancer action was attributed to the suppression of EGFR-TK. It also significantly suppressed the tumor growth in Hep-2 cell xenograft model.
受肉桂卓越抗癌活性的启发,开展本研究以阐明肉桂精油(EOC)的抗癌潜力。
采用MTT法检测EOC对人头颈部鳞状细胞癌(HNSCC)的多种细胞系(FaDu、Detroit - 562和SCC - 25)的作用。利用Hep - 2细胞异种移植模型评估EOC的阳性生物活性。还进行了EGFR - TK抑制试验以解释EOC可能的作用机制。此外,为阐明负责减弱EGFR的关键相互作用,对通过GC - MS分析鉴定出的EOC主要成分反式肉桂醛,进行了与EGFR蛋白模型催化结构域的分子对接实验。
EOC对FaDu、Detroit - 562和SCC - 25的抑制率分别为66.12%、87.32%和99.34%,显示出显著的抗癌活性。此外,在Hep - 2细胞异种移植模型中,EOC使肿瘤负担降低至43.5%,同时在EGFR - TK抑制试验中对EGFR - TK活性的抑制率达89%。对接实验表明,反式肉桂醛通过与关键催化残基Val702、Ala719、Lys721、Leu764、Thr766和Leu820形成紧密的原子间接触,有效地契合到EGFR活性位点的内部凹槽中,抑制常数Ki = 775.93 μM。
EOC在体外对HNSCC细胞具有显著的抗癌活性。其抗癌作用的潜在机制归因于对EGFR - TK的抑制。它还在Hep - 2细胞异种移植模型中显著抑制了肿瘤生长。