现代肿瘤医学
現代腫瘤醫學
현대종류의학
JOURNAL OF MODERN ONCOLOGY
2014年
9期
2006-2009
,共4页
潘洪飞%任大鹏%孟凡东%田昕%李妍
潘洪飛%任大鵬%孟凡東%田昕%李妍
반홍비%임대붕%맹범동%전흔%리연
口腔鳞状细胞癌%半乳糖凝集素-1%缺氧
口腔鱗狀細胞癌%半乳糖凝集素-1%缺氧
구강린상세포암%반유당응집소-1%결양
oral squamous cell carcinoma cells%Galectin-1%hypoxic
目的:探讨缺氧条件下Galectin-1对口腔鳞癌细胞Tca8113的生物学行为的影响。方法:siRNA干扰Galectin-1在Tca8113细胞中的表达;采用MTT法检测细胞的增殖;Real time-PCR分析Galectin-1 mR-NA和Bcl-2 mRNA的表达;Transwell小室观察各组细胞的侵袭能力;免疫荧光分析缺氧条件下细胞的凋亡情况。结果:siRNA-Galectin-l干扰组和200μmol/L氯化钴处理组的细胞出现了增殖抑制;用200μmol/L氯化钴处理Tca8113细胞后,Galectin-l mRNA的表达量上调(0.91±0.11,P<0.05);siRNA+Tca8113细胞组Bcl-2 mRNA的表达量明显减低(0.16±0.02,P<0.05);siRNA-Galectin-l干扰组迁移出的细胞数(31±6)明显低于200μmol/L氯化钴+Tca8113细胞组(43±6)和Tca8113细胞组(51±8,P<0.05);免疫荧光结果所示,siRNA+200μmol/L氯化钴+Tca8113细胞组的荧光强度最弱。结论:Galectin-1是反应肿瘤细胞缺氧的一个较为敏感的指标,可利用Galectin-1作为内在的缺氧标志物。
目的:探討缺氧條件下Galectin-1對口腔鱗癌細胞Tca8113的生物學行為的影響。方法:siRNA榦擾Galectin-1在Tca8113細胞中的錶達;採用MTT法檢測細胞的增殖;Real time-PCR分析Galectin-1 mR-NA和Bcl-2 mRNA的錶達;Transwell小室觀察各組細胞的侵襲能力;免疫熒光分析缺氧條件下細胞的凋亡情況。結果:siRNA-Galectin-l榦擾組和200μmol/L氯化鈷處理組的細胞齣現瞭增殖抑製;用200μmol/L氯化鈷處理Tca8113細胞後,Galectin-l mRNA的錶達量上調(0.91±0.11,P<0.05);siRNA+Tca8113細胞組Bcl-2 mRNA的錶達量明顯減低(0.16±0.02,P<0.05);siRNA-Galectin-l榦擾組遷移齣的細胞數(31±6)明顯低于200μmol/L氯化鈷+Tca8113細胞組(43±6)和Tca8113細胞組(51±8,P<0.05);免疫熒光結果所示,siRNA+200μmol/L氯化鈷+Tca8113細胞組的熒光彊度最弱。結論:Galectin-1是反應腫瘤細胞缺氧的一箇較為敏感的指標,可利用Galectin-1作為內在的缺氧標誌物。
목적:탐토결양조건하Galectin-1대구강린암세포Tca8113적생물학행위적영향。방법:siRNA간우Galectin-1재Tca8113세포중적표체;채용MTT법검측세포적증식;Real time-PCR분석Galectin-1 mR-NA화Bcl-2 mRNA적표체;Transwell소실관찰각조세포적침습능력;면역형광분석결양조건하세포적조망정황。결과:siRNA-Galectin-l간우조화200μmol/L록화고처리조적세포출현료증식억제;용200μmol/L록화고처리Tca8113세포후,Galectin-l mRNA적표체량상조(0.91±0.11,P<0.05);siRNA+Tca8113세포조Bcl-2 mRNA적표체량명현감저(0.16±0.02,P<0.05);siRNA-Galectin-l간우조천이출적세포수(31±6)명현저우200μmol/L록화고+Tca8113세포조(43±6)화Tca8113세포조(51±8,P<0.05);면역형광결과소시,siRNA+200μmol/L록화고+Tca8113세포조적형광강도최약。결론:Galectin-1시반응종류세포결양적일개교위민감적지표,가이용Galectin-1작위내재적결양표지물。
Objective:The biological effects of Galectin-l for oral squamous cell carcinoma cells in hypoxic envi-ronment were investigated.Methods:To interfere the expression of Galectin-1 in cells with siRNA,the proliferation of cells was detected by MTT methods;the expression of Galectin-1 mRNA and Bcl-2 mRNA were analysed by real time-PCR,using Transwell to detect the invasion ability;to analyse the condition of cell apoptosis in hypoxic by im-munofluorescence.Results:siRNA-Galectin-l group and 200μmol/L CoCl2 group appeared the inhibition of prolif-eration,the expression of Galectin-1 mRNA was significantly increased in 200μmol/L CoCl2 group (0.91 ±0.11,P<0.05),the expression of Bcl-2 mRNA was significantly reduced in siRNA group (0.16 ±0.02,P<0.05);the cell counts of siRNA-Galectin-l interference group (31 ±6)was significantly lower than 200μmol/L CoCl2 group (43 ±6)was Tca8113 cell group (51 ±8,P<0.05),the fluorescence intensity of siRNA and 200μmol/L CoCl2 and Tca8113 cell group were the weakest.Conclusion:Galectin-1 was a sensitive indicator with tumor cells in hypoxic environment,Galectin-1 maybe used as an inner oxygen marker.