中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2012年
12期
2393-2395
,共3页
李瑞晓%于垂恭%张璟%袁建林%武国军
李瑞曉%于垂恭%張璟%袁建林%武國軍
리서효%우수공%장경%원건림%무국군
膀胱肿瘤%抑癌基因%腺病毒
膀胱腫瘤%抑癌基因%腺病毒
방광종류%억암기인%선병독
Bladder neoplasms%Antioncogene%Adenovirus
目的 观察抑癌基因N-MYC下游调节基因-2(NDRG2)在不同膀胱癌细胞株的表达水平及对T24细胞体外增殖的抑制作用.方法 采用Western blot及逆转录-聚合酶链反应(RT-PCR)检测3种膀胱癌细胞及正常上皮组织细胞的NDRG2表达,使用pAD-CMV腺病毒感染的方法观察NDRG2对T24细胞的作用,乳糖操纵子z(Lacz)为阳性对照,并设空白对照,流式细胞仪(FCM)连续检测细胞的周期及凋亡.结果 3种膀胱癌细胞株的NDRG2表达水平相对较低,其中T24细胞表达水平最低,FCM检测显示,感染组同阳性对照组及空白组比较,细胞G1期阻滞[3组分别为(56.26 ±3.02)%、(50.39±3.13)%和(47.41±2.63)%],细胞凋亡增加[3组分别为(12.06±1.33)%、(4.27±1.01)%和(2.45±0.86)%].结论 NDRG2基因可能参与了膀胱癌的发病,腺病毒介导的人NDRG2基因可抑制T24细胞的增殖.
目的 觀察抑癌基因N-MYC下遊調節基因-2(NDRG2)在不同膀胱癌細胞株的錶達水平及對T24細胞體外增殖的抑製作用.方法 採用Western blot及逆轉錄-聚閤酶鏈反應(RT-PCR)檢測3種膀胱癌細胞及正常上皮組織細胞的NDRG2錶達,使用pAD-CMV腺病毒感染的方法觀察NDRG2對T24細胞的作用,乳糖操縱子z(Lacz)為暘性對照,併設空白對照,流式細胞儀(FCM)連續檢測細胞的週期及凋亡.結果 3種膀胱癌細胞株的NDRG2錶達水平相對較低,其中T24細胞錶達水平最低,FCM檢測顯示,感染組同暘性對照組及空白組比較,細胞G1期阻滯[3組分彆為(56.26 ±3.02)%、(50.39±3.13)%和(47.41±2.63)%],細胞凋亡增加[3組分彆為(12.06±1.33)%、(4.27±1.01)%和(2.45±0.86)%].結論 NDRG2基因可能參與瞭膀胱癌的髮病,腺病毒介導的人NDRG2基因可抑製T24細胞的增殖.
목적 관찰억암기인N-MYC하유조절기인-2(NDRG2)재불동방광암세포주적표체수평급대T24세포체외증식적억제작용.방법 채용Western blot급역전록-취합매련반응(RT-PCR)검측3충방광암세포급정상상피조직세포적NDRG2표체,사용pAD-CMV선병독감염적방법관찰NDRG2대T24세포적작용,유당조종자z(Lacz)위양성대조,병설공백대조,류식세포의(FCM)련속검측세포적주기급조망.결과 3충방광암세포주적NDRG2표체수평상대교저,기중T24세포표체수평최저,FCM검측현시,감염조동양성대조조급공백조비교,세포G1기조체[3조분별위(56.26 ±3.02)%、(50.39±3.13)%화(47.41±2.63)%],세포조망증가[3조분별위(12.06±1.33)%、(4.27±1.01)%화(2.45±0.86)%].결론 NDRG2기인가능삼여료방광암적발병,선병독개도적인NDRG2기인가억제T24세포적증식.
Objective To detect the expression level of N-MYC down-stream regulated gene-2 (NDRG2) in different bladder carcinoma cell lines,and investigate the inhibitory effects of NDRG2 on proliferation of T24 cells mediated by adenovirus in vitro.Methods The expression of NDRG2 protein and mRNA was detected by using Western blotting and reverse transcription-polymerase chain reaction (RT-PCR) respectively in three bladder cancer cell lines.PAD-NDRG2 adenoviruses were used to infect the T24 cells.The changes in cell cycle and apoptosis were detected by using flow cytometry (FCM) at the 72nd h after the infection.Results The results of Western blotting and RT-PCR revealed that the three bladder carcinoma cell lines had relatively lower NDRG2 protein and mRNA expression levels.T24 cells had the lowest level among the three cell lines.As compared with the positive control and the blank control,pAD-CMV-NDRG2-infected cells showed an increase in G1 phase at 72rid h [(56.26 ± 3.02) %,(50.39 ±3.13)% and (47.41 ±2.63)% respectively].Furthermore,NDRG2-induced apoptosis was also increased at 72nd h in comparison with the controls [(12.06 ± 1.33)%,(4.27 ± 1.01)% and (2.45 ±0.86%)%].Conclusion The NDRG2 might be involved in the pathogenesis of bladder carcinoma.Adenovirus-mediated NDRG2 could suppress the proliferation of T24 cells significantly.