北京口腔医学
北京口腔醫學
북경구강의학
BEIJING JOURNAL OF STOMATOLOGY
2014年
6期
307-310
,共4页
牛文雯%张敏%景新颖%董蕊%张剑飞%汤晓飞
牛文雯%張敏%景新穎%董蕊%張劍飛%湯曉飛
우문문%장민%경신영%동예%장검비%탕효비
口腔鳞状细胞癌%α3-nAChR%α7-nAChR
口腔鱗狀細胞癌%α3-nAChR%α7-nAChR
구강린상세포암%α3-nAChR%α7-nAChR
Oral squamous cell carcinoma%α3-nAChR%α7-nAChR
目的:研究烟碱型乙酰胆碱受体α3-nAChR和α7-nAChR在口腔鳞状细胞癌( oral squamous cell carcinoma, OSCC)中的表达,为口腔癌发病机制的研究提供实验依据。方法随机选取20例福尔马林固定的口腔鳞状细胞癌组织标本,10例正常口腔黏膜作为对照。采用免疫组织化学染色和荧光定量PCR方法,检测烟碱型乙酰胆碱受体α3-nAChR和α7-nAChR在OSCC中的表达。结果口腔鳞状细胞癌中α3-nAChR的mRNA水平是正常口腔黏膜的3.97倍( P <0.05),蛋白表达水平显著高于正常口腔黏膜( P <0.05),α7-nAChR 的mRNA水平是正常口腔黏膜的8.41倍( P<0.05),蛋白表达水平也显著高于正常口腔黏膜( P<0.05)。结论α3-nAChR、α7-nAChR与烟草相关口腔鳞状细胞癌的发生密切相关,在 OSCC治疗中有望成为有价值的分子靶点。
目的:研究煙堿型乙酰膽堿受體α3-nAChR和α7-nAChR在口腔鱗狀細胞癌( oral squamous cell carcinoma, OSCC)中的錶達,為口腔癌髮病機製的研究提供實驗依據。方法隨機選取20例福爾馬林固定的口腔鱗狀細胞癌組織標本,10例正常口腔黏膜作為對照。採用免疫組織化學染色和熒光定量PCR方法,檢測煙堿型乙酰膽堿受體α3-nAChR和α7-nAChR在OSCC中的錶達。結果口腔鱗狀細胞癌中α3-nAChR的mRNA水平是正常口腔黏膜的3.97倍( P <0.05),蛋白錶達水平顯著高于正常口腔黏膜( P <0.05),α7-nAChR 的mRNA水平是正常口腔黏膜的8.41倍( P<0.05),蛋白錶達水平也顯著高于正常口腔黏膜( P<0.05)。結論α3-nAChR、α7-nAChR與煙草相關口腔鱗狀細胞癌的髮生密切相關,在 OSCC治療中有望成為有價值的分子靶點。
목적:연구연감형을선담감수체α3-nAChR화α7-nAChR재구강린상세포암( oral squamous cell carcinoma, OSCC)중적표체,위구강암발병궤제적연구제공실험의거。방법수궤선취20례복이마림고정적구강린상세포암조직표본,10례정상구강점막작위대조。채용면역조직화학염색화형광정량PCR방법,검측연감형을선담감수체α3-nAChR화α7-nAChR재OSCC중적표체。결과구강린상세포암중α3-nAChR적mRNA수평시정상구강점막적3.97배( P <0.05),단백표체수평현저고우정상구강점막( P <0.05),α7-nAChR 적mRNA수평시정상구강점막적8.41배( P<0.05),단백표체수평야현저고우정상구강점막( P<0.05)。결론α3-nAChR、α7-nAChR여연초상관구강린상세포암적발생밀절상관,재 OSCC치료중유망성위유개치적분자파점。
Objective To investigate the expression ofα3-nAChR andα7-nAChR in oral squamous cell carcinoma ( OSCC) and the pathogenesis of tobacco related OSCC. Methods Twenty cases of formalin fixed OSCC tissue samples were randomly selected, and ten cases of normal oral mucosa tissues served as control. The expression of α3-nAChR andα7-nAChR was examined by immunohistochemistry and real-time quantitative PCR. Results Compared with normal oral mucosa,α3-nAChR and α7-nAChR mRNA level and protein expression were increased in oral squamous cell carcinoma ( P<0. 05 ) . Conclusion α3-nAChR and α7-nAChR may be closely related to the occurrence of tobacco-related oral squamous cell carcinoma, and hopefully become therapeutic targets in oral squamous cell carcinoma.