实用癌症杂志
實用癌癥雜誌
실용암증잡지
THE PRACTICAL JOURNAL OF CANCER
2015年
9期
1269-1272
,共4页
梁赅%杜伟%李爽%柯庆华%蔡君%杨继元
樑賅%杜偉%李爽%柯慶華%蔡君%楊繼元
량해%두위%리상%가경화%채군%양계원
胃癌细胞%低氧%CD44%HIF1α
胃癌細胞%低氧%CD44%HIF1α
위암세포%저양%CD44%HIF1α
Gastric cancer cell%Hypoxia%CD44%HIF1α
目的:研究低氧条件下胃癌细胞HIF1α及CD44的表达变化,并观察下调HIF1α表达对CD44表达的影响。方法以人胃癌细胞系SGC7901细胞为研究对象,分别于正常氧压及含1% O2条件下传代培养1周。随后加入20 nm/L雷帕霉素培养72 h,CCK8法检测细胞活力,Transwell试验检测细胞侵袭能力,实时定量PCR及western blot检测CD44及HIF1α的mRNA及蛋白表达。结果与正常组对比,低氧条件下细胞增殖活性明显升高(P<0.05),侵袭活性明显增强(P<0.05),HIF1α及CD44基因的mRNA及蛋白表达水平明显升高(P<0.01)。雷帕霉素处理后,不论在常氧及低氧条件下细胞活力均较对照组弱(P<0.05),细胞侵袭活性明显下降(P<0.05)。细胞HIF1α和CD44的mRNA及蛋白表达水平均明显降低(P<0.01)。结论低氧条件下胃癌细胞SGC7901增殖及侵袭能力明显增强,下调细胞的HIF1α表达后,显著降低CD44的表达。由此可推测,低氧可能通过HIF1α调节CD44的表达,调控胃癌细胞增殖及侵袭潜能。
目的:研究低氧條件下胃癌細胞HIF1α及CD44的錶達變化,併觀察下調HIF1α錶達對CD44錶達的影響。方法以人胃癌細胞繫SGC7901細胞為研究對象,分彆于正常氧壓及含1% O2條件下傳代培養1週。隨後加入20 nm/L雷帕黴素培養72 h,CCK8法檢測細胞活力,Transwell試驗檢測細胞侵襲能力,實時定量PCR及western blot檢測CD44及HIF1α的mRNA及蛋白錶達。結果與正常組對比,低氧條件下細胞增殖活性明顯升高(P<0.05),侵襲活性明顯增彊(P<0.05),HIF1α及CD44基因的mRNA及蛋白錶達水平明顯升高(P<0.01)。雷帕黴素處理後,不論在常氧及低氧條件下細胞活力均較對照組弱(P<0.05),細胞侵襲活性明顯下降(P<0.05)。細胞HIF1α和CD44的mRNA及蛋白錶達水平均明顯降低(P<0.01)。結論低氧條件下胃癌細胞SGC7901增殖及侵襲能力明顯增彊,下調細胞的HIF1α錶達後,顯著降低CD44的錶達。由此可推測,低氧可能通過HIF1α調節CD44的錶達,調控胃癌細胞增殖及侵襲潛能。
목적:연구저양조건하위암세포HIF1α급CD44적표체변화,병관찰하조HIF1α표체대CD44표체적영향。방법이인위암세포계SGC7901세포위연구대상,분별우정상양압급함1% O2조건하전대배양1주。수후가입20 nm/L뢰파매소배양72 h,CCK8법검측세포활력,Transwell시험검측세포침습능력,실시정량PCR급western blot검측CD44급HIF1α적mRNA급단백표체。결과여정상조대비,저양조건하세포증식활성명현승고(P<0.05),침습활성명현증강(P<0.05),HIF1α급CD44기인적mRNA급단백표체수평명현승고(P<0.01)。뢰파매소처리후,불론재상양급저양조건하세포활력균교대조조약(P<0.05),세포침습활성명현하강(P<0.05)。세포HIF1α화CD44적mRNA급단백표체수평균명현강저(P<0.01)。결론저양조건하위암세포SGC7901증식급침습능력명현증강,하조세포적HIF1α표체후,현저강저CD44적표체。유차가추측,저양가능통과HIF1α조절CD44적표체,조공위암세포증식급침습잠능。
Objective To observe the change of expression of HIF1αand CD44 in human gastric cell line SGC7901 in hypoxia,and the effect of down-regulating HIF1αexpression on CD44 expression.Methods SGC7901 cells were cultured in 1%O2 condition for 1 week,and then treated with 20 nm/L rapamycin for 72 h.Cell viability was measured by CCK8 assay.Cell inva-sion was detected by Transwell invasion assay.Protein and mRNA expression of HIF1αand CD44 was detected by Western blot-ting and real-time RT-PCR.Results Compared with the control group,cell viability and invasion obviously increased in hypoxia (P<0.05),but decreased after treated with rapamycin (P<0.05).Protein and mRNA expression of HIF1αand CD44 obviously decreased in hypoxia (P<0.05),and inhibited by rapamycin (P<0.05).Conclusion In hypoxia,the proliferation and inva-sion of SGC7901 increased,and down-regulating the expression of HIF1αcan significantly inhibit CD44 expression.Therefore,it is possible that hypoxia can regulate the CD44 expression of gastric cancer cell via HIF1α,and regulate cell proliferation and inva-sion.