染色质解旋酶DNA结合蛋白对舌鳞状细胞癌CAL27细胞侵袭和转移影响的研究  

Effect of chromodomain helicase/ATPase DNA binding protein 1-like gene on the invasion and metastasis of tongue squamous cell carcinoma CAL27 cells

作　　者：胡凯莉 范欣[2] 胡温庭[3] 李洪利 唐清华 孙学辉[3] Hu Kaili;Fan Xin;Hu Wenting;Li Hongli;Tang Qinghua;Sun Xuehui(School of Stomatology,Weifang Medical University,Weifang 261053,China;Dept.of Dentistry,The Affiliated Hospital of Weifang Medical University,Weifang 261000,China;Dept.of Oral and Maxillofacial Surgery,The Affiliated Hospital of Weifang Medical University,Weifang 261000,China;Medicine Research Center,Weifang Medical University,Weifang 261053,China)

机构地区：[1]潍坊医学院口腔医学院,潍坊261053 [2]潍坊医学院附属医院口腔科,潍坊261000 [3]潍坊医学院附属医院口腔颌面外科,潍坊261000 [4]潍坊医学院医学研究实验中心,潍坊261053

出　　处：《华西口腔医学杂志》2021年第1期81-87,共7页West China Journal of Stomatology

基　　金：国家自然科学基金青年科学基金(81702932)。

摘　　要：目的探讨染色质解旋酶DNA结合蛋白(CHD1L)影响舌鳞状细胞癌侵袭和转移的分子机制,为临床抑制舌鳞状细胞癌的侵袭和转移提供新的靶点。方法运用Ualcan网站分析CHD1L在正常上皮组织和原发性头颈鳞状细胞癌组织中的表达情况,分析有无淋巴结转移对头颈鳞状细胞癌组织中CHD1L表达情况的影响;通过GEPIA网站分析CHD1L在头颈鳞状细胞癌中的表达与生存率的关系;蛋白质印迹法检测人舌鳞状细胞癌细胞CAL27和人正常皮肤细胞HaCaT中CHD1L蛋白的表达水平;用RNA干扰质粒敲低人舌鳞状细胞癌细胞CAL27中的CHD1L后,将细胞分别命名为SiCHD1L/CAL27及Scr/CAL27;蛋白质印迹法检测CHD1L在每组细胞中的表达情况;EdU增殖实验检测每组细胞增殖能力的改变;伤口愈合实验检测每组细胞迁移能力的改变;蛋白质印迹法检测上皮间质转化(EMT)标志物上皮钙黏着蛋白和波形蛋白的表达水平。结果Ualcan数据库显示:CHD1L在原发头颈鳞状细胞癌组织中表达高于正常上皮组织中的表达,在出现淋巴结转移的头颈鳞状细胞癌组织中表达更高。GEPIA网站分析显示:CHD1L表达量高的头颈鳞状细胞癌患者总生存率较表达量低的患者明显降低。蛋白质印迹结果显示:人舌鳞状细胞癌细胞CAL27中CHD1L表达高于人正常皮肤细胞HaCaT中CHD1L的表达,敲低CHD1L以后CAL27细胞中CHD1L的表达量明显低于Scr/CAL27组细胞。EdU增殖实验结果显示:SiCHD1L/CAL27组细胞增殖能力明显降低。伤口愈合实验显示:SiCHD1L/CAL27组迁移能力降低,SiCHD1L/CAL27组细胞上皮钙黏着蛋白表达量增加而波形蛋白表达量降低。结论CHD1L促进舌鳞状细胞癌细胞的EMT,促进舌鳞状细胞癌细胞的增殖、迁移侵袭能力。Objective A study was conducted to investigate the molecular mechanism of chromodomain helicase/ATPase DNA binding protein 1-like gene(CHD1L)influencing the invasion and metastasis of tongue squamous cell carcinoma and to provide a new target for clinical inhibition of invasion and metastasis of tongue squamous cell carcinoma.Methods Ualcan website was used to analyze the expression of CHD1L in normal epithelial tissue and primary head and neck squamous cell carcinoma and to analyze the effect of lymph node metastasis on the expression of CHD1L in tissues with head and neck squamous cell carcinoma.The relationship between CHD1L expression and the survival rate of patients with head and neck squamous cell carcinoma was tested by the GEPIA website.Western blot was used to quantify the levels of CHD1L protein in human tongue squamous cell carcinoma CAL27 and immortalized human skin keratinocyte cell HaCaT.After knocking down CAL27 in human tongue squamous cell carcinoma cells with an RNA interference plasmid,the cells were designated as SiCHD1L/CAL27 and Scr/CAL27.Western blot was utilized to detect the expression of CHD1L in each group of cells.The change in CAL27 cell proliferation ability was tested by EdU proliferation test after CHD1L knockdown.The change of cell migration ability of each group cells was tested through the wound healing assay.Western blot was used to detect epithelial-mesenchymal transition(EMT)marker E-cadherin and Vimentin protein expression levels.Results Ualcan database showed that the expression of CHD1L in primary head and neck squamous cell carcinoma tissues was higher than in normal epithelial tissues and in head and neck squamous cell carcinoma tissues with lymph node metastasis.GEPIA website analysis showed that the overall survival rate of patients with head and neck squamous cell carcinoma with high expression of CHD1L was significantly lower than that of patients with low expression.Western blot results showed that CHD1L expression in human tongue squamous carcinoma cells CAL27 was

关 键 词：舌鳞状细胞癌 染色质解旋酶DNA结合蛋白 上皮间质转化 增殖 侵袭 

分 类 号：R739.86[医药卫生—肿瘤]