首页|柠檬精油活性成分柠檬醛抑制头颈癌细胞增殖的机制研究

柠檬精油活性成分柠檬醛抑制头颈癌细胞增殖的机制研究

扫码查看
探索柠檬精油中发挥抗肿瘤作用的活性物质以及抑制头颈癌细胞SCC15 和CAL33 增殖的分子机制,该研究利用噻唑蓝[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay,MTT]鉴定出抑制头颈癌细胞增殖的活性物质为柠檬醛,并测定了柠檬醛抑制头颈癌细胞和正常细胞的IC50;同时,利用 5-ethynyl-2'-deoxyuridine(EdU)实验检测柠檬醛对头颈癌细胞增殖率的影响,通过克隆形成实验检测柠檬醛对头颈癌细胞体外肿瘤球形成的影响。通过流式细胞术检测柠檬醛对头颈癌细胞周期阻滞和凋亡诱导情况;采用蛋白印迹检测柠檬醛对头颈癌细胞周期和凋亡相关蛋白表达水平的影响。结果表明柠檬醛可有效抑制头颈癌细胞的生长增殖,具有抗肿瘤活性,其抑制CAL33 和SCC15 的半数抑制浓度分别为 54。78、25。23 μg·mL-1。进一步分析发现细胞周期相关蛋白 S期激酶关联蛋白 2(SKP2)、原癌基因(C-MYC)、细胞周期依赖性激酶 1(CDK1)、周期蛋白B(cyclin B)均呈下调趋势,细胞周期阻滞于G2/M期。此外,柠檬醛能够促使细胞凋亡相关蛋白半胱天冬蛋白酶-3(caspase-3)、半胱天冬蛋白酶-9(caspase-9)和多聚腺苷二磷酸核糖聚合酶(PARP)剪切形式呈现上调趋势,而且使自噬相关蛋白微管相关蛋白 1 轻链 3B(LC3B)、泛素结合蛋白(P62)、自噬效应蛋白Beclin1(Beclin1)和溶酶体相关膜蛋白 1(LAMP1)表达呈上调趋势,暗示柠檬醛诱导头颈癌细胞发生凋亡和激活自噬。利用双标质粒系统mCherry-GFP-LC3 分析发现柠檬醛阻碍自噬体和溶酶体融合,使自噬流进程受阻。因此,柠檬精油中发挥抗头颈癌细胞增殖的主要活性成分是柠檬醛,该成分对头颈癌细胞具有显著的抑制作用,其分子机制可能是柠檬醛通过阻滞细胞周期,诱导细胞发生凋亡和自噬,最终抑制肿瘤细胞增殖。
Study on mechanism of inhibiting proliferation of head and neck cancer cells by citral,active ingredient of lemon essential oil
To explore the active substances exerting anti-tumour effect in lemon essential oil and the molecular mechanism inhibiting the proliferation of head and neck cancer cells SCC15 and CAL33,3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay(MTT)was utilized to identify the active component inhibiting the proliferation of head and neck cancer cells,namely citral.The IC50 of citral inhibiting the proliferation of head and neck cancer cells and normal cells were also determined.In addition,a 5-ethynyl-2'-deoxyuridine(EdU)staining assay was used to detect the effect of citral on the proliferation rate of head and neck cancer cells,and a colony formation assay was used to detect the effect of citral on tumor sphere formation of head and neck cancer cells in vitro.The cell cycle arrest and apoptosis induction of head and neck cancer cells by citral were evaluated by flow cytometry,and Western blot was used to detect the effect of citral on the expression levels of cell cycle-and apoptosis-related proteins in head and neck cancer cells.The findings indicated that citral could effectively inhibit the proliferation and growth of head and neck cancer cells,with anti-tumor activity,and its half inhibitory concentrations for CAL33 and SCC15 were 54.78 and 25.23 μg·mL-1,respectively.Furthermore,citral arrested cell cycle at G2/M phase by down-regulating cell cycle-related proteins such as S-phase kinase associated protein 2(SKP2),C-MYC,cyclin dependent kinase 1(CDK1),and cyclin B.Moreover,citral increased the cysteinyl aspartate-specific proteinase-3(caspase-3),cysteinyl aspartate-specific proteinase-9(caspase-9),and cleaved poly ADP-ribose polymerase(PARP).It up-regulated the level of autophagy-related proteins including microtubule associated protein 1 light chain 3B(LC3B),sequestosome 1(P62/SQSTM1),autophagy effector protein Beclin1(Beclin1),and lysosome-associate membrane protein 1(LAMP1),suggesting that citral could effectively trigger cell apoptosis and cell autophagy in head and neck cancer cells.Furthermore,the dual-tagged plasmid system mCherry-GFP-LC3 was used,and it was found that citral impeded the fusion of autophagosomes and lysosomes,leading to autophagic flux blockage.Collectively,our findings reveal that the main active anti-proliferation component of lemon essential oil is citral,and this component has a significant inhibitory effect on head and neck cancer cells.Its underlying molecular mechanism is that citral induces apoptosis and autophagy by cell cycle arrest and ultimately inhibits cell proliferation.

citralhead and neck canceranti-tumorapoptosisautophagy

陈利、张亚军、秦洪文、胡武静、刘俨娇、肖国生、杜慧慧、杨东林

展开 >

重庆三峡学院 生物与食品工程学院,重庆 404120

重庆文理学院 药学院(创新靶向药物国际研究院),重庆 402160

柠檬醛 头颈癌 抗肿瘤 凋亡 自噬

重庆市教委科学技术研究计划重庆市教委科学技术研究计划重庆市教委科技项目青年项目重庆三峡学院人才项目重庆三峡学院研究生科研创新项目

KJQN202201205KJQN202201330KJQN20200120520RC-12YJSKY23029

2024

中国中药杂志
中国药学会

中国中药杂志

CSTPCD北大核心
影响因子:1.718
ISSN:1001-5302
年,卷(期):2024.49(9)
  • 36