中国免疫学杂志
中國免疫學雜誌
중국면역학잡지
CHINESE JOURNAL OF IMMUNOLOGY
2015年
9期
1210-1213
,共4页
丁陈波%冯继红%杨丽文%李龙梅%李姗姗%陈超%罗军敏
丁陳波%馮繼紅%楊麗文%李龍梅%李姍姍%陳超%囉軍敏
정진파%풍계홍%양려문%리룡매%리산산%진초%라군민
Gab2%结直肠癌%慢病毒%增殖%迁移
Gab2%結直腸癌%慢病毒%增殖%遷移
Gab2%결직장암%만병독%증식%천이
Gab2%Colorectal cancer%Lentivirus%Proliferation%Migration
目的:探讨Gab2过表达对人结直肠癌细胞株SW480增殖和迁移能力的影响。方法:用携带Gab2基因的重组慢病毒颗粒( LV-Gab2-GFP)感染人结直肠癌SW480细胞株,作为实验组( LV-Gab2-GFP 组);以对照慢病毒颗粒( LV-GFP)感染人结直肠癌SW480细胞株,作为阴性对照组( LV-GFP组);空白对照组常规培养,不作任何处理。用RT-PCR和Western blot法分别检测细胞中Gab2 mRNA和蛋白表达的水平;CCK-8法和平板克隆实验检测细胞增殖能力的变化;划痕愈合实验检测细胞迁移能力的变化。结果:RT-PCR和Western blot均显示LV-Gab2-GFP组Gab2的表达均较对照组显著增高;与对照组比较,Gab2过表达显著增强人结直肠癌SW480细胞的增殖和迁移能力。结论:Gab2过表达可以促进SW480细胞增殖和迁移能力。
目的:探討Gab2過錶達對人結直腸癌細胞株SW480增殖和遷移能力的影響。方法:用攜帶Gab2基因的重組慢病毒顆粒( LV-Gab2-GFP)感染人結直腸癌SW480細胞株,作為實驗組( LV-Gab2-GFP 組);以對照慢病毒顆粒( LV-GFP)感染人結直腸癌SW480細胞株,作為陰性對照組( LV-GFP組);空白對照組常規培養,不作任何處理。用RT-PCR和Western blot法分彆檢測細胞中Gab2 mRNA和蛋白錶達的水平;CCK-8法和平闆剋隆實驗檢測細胞增殖能力的變化;劃痕愈閤實驗檢測細胞遷移能力的變化。結果:RT-PCR和Western blot均顯示LV-Gab2-GFP組Gab2的錶達均較對照組顯著增高;與對照組比較,Gab2過錶達顯著增彊人結直腸癌SW480細胞的增殖和遷移能力。結論:Gab2過錶達可以促進SW480細胞增殖和遷移能力。
목적:탐토Gab2과표체대인결직장암세포주SW480증식화천이능력적영향。방법:용휴대Gab2기인적중조만병독과립( LV-Gab2-GFP)감염인결직장암SW480세포주,작위실험조( LV-Gab2-GFP 조);이대조만병독과립( LV-GFP)감염인결직장암SW480세포주,작위음성대조조( LV-GFP조);공백대조조상규배양,불작임하처리。용RT-PCR화Western blot법분별검측세포중Gab2 mRNA화단백표체적수평;CCK-8법화평판극륭실험검측세포증식능력적변화;화흔유합실험검측세포천이능력적변화。결과:RT-PCR화Western blot균현시LV-Gab2-GFP조Gab2적표체균교대조조현저증고;여대조조비교,Gab2과표체현저증강인결직장암SW480세포적증식화천이능력。결론:Gab2과표체가이촉진SW480세포증식화천이능력。
Objective:To investigate the effects of Gab2 overexpression on the proliferation and migration of human colorectal cancer cell line SW480.Methods: The experimental group (LV-Gab2-GFP group),colorectal cancer SW480 cells were transfected with recombinant lentivirus vector (LV-Gab2-GFP),the negative control group was transfected with negative control lentiviral vector ( LV-GFP) ,and the blank control group without any treatment.The mRNA and protein expression of Gab 2 in cells were identified by RT-PCR and Western blot respectively.Proliferation of the cells was detected by CCK-8 colorimeter and colony forming assay.Wound-healing assay was used to determine the cells migration .Results: RT-PCR and Western blot demonstrated that Gab 2 mRNA and protein expression significantly increased in LV-Gab2-GFP group compared with control groups;overexpression of Gab2 markedly enhanced human colorectal cancer SW 480 cells proliferation and migration compared with control groups .Conclusion:Overexpression of Gab2 accelerates human colorectal cancer SW 480 cells proliferation and migration.