南昌大学学报(医学版)
南昌大學學報(醫學版)
남창대학학보(의학판)
Acta Academiae Medicinae Jiangxi
2015年
5期
19-24
,共6页
余秋芳%王美凤%刘春菊%万慧芳%张霞丽%万福生
餘鞦芳%王美鳳%劉春菊%萬慧芳%張霞麗%萬福生
여추방%왕미봉%류춘국%만혜방%장하려%만복생
p53 上调凋亡调制因子%非小细胞肺癌%细胞增殖%凋亡
p53 上調凋亡調製因子%非小細胞肺癌%細胞增殖%凋亡
p53 상조조망조제인자%비소세포폐암%세포증식%조망
p53 up-regulated modulator of apoptosis%non-small cell lung cancer%cell proliferation%apoptosis
目的:探讨外源性 p53上调凋亡调制因子(PUMA)对非小细胞肺癌 A549细胞增殖、凋亡的影响。方法将肺癌A549细胞分为 Control 组、空载体组、PUMA 组(转染 pCEP4-(HA)2-PUMA 质粒),DDP 组(10μg· mL-1)和 PUMA+DDP 组(转染 pCEP4-(HA)2-PUMA 质粒,加10μg·mL-1顺铂)5个组。细胞生存率和凋亡率分别用 MTT 法和流式细胞仪检测,细胞 PUMA、Bax 及 Bcl-2蛋白表达水平采用 Western blot 方法检测。结果与 Control 组比较:PUMA 组、DDP 组及 PUMA+DDP 组 A549细胞增殖均显著降低(P <0.01),且 PUMA+DDP组降低程度最强(P <0.01);凋亡率均显著升高(P <0.01);Bax 蛋白水平呈显著性升高(P <0.01),Bcl-2蛋白呈显著性下降(P <0.01)。结论外源性 PUMA 可抑制肺癌 A549细胞增殖,促进凋亡,其机制与增加细胞 Bax 蛋白表达,降低 Bcl-2蛋白表达有关。
目的:探討外源性 p53上調凋亡調製因子(PUMA)對非小細胞肺癌 A549細胞增殖、凋亡的影響。方法將肺癌A549細胞分為 Control 組、空載體組、PUMA 組(轉染 pCEP4-(HA)2-PUMA 質粒),DDP 組(10μg· mL-1)和 PUMA+DDP 組(轉染 pCEP4-(HA)2-PUMA 質粒,加10μg·mL-1順鉑)5箇組。細胞生存率和凋亡率分彆用 MTT 法和流式細胞儀檢測,細胞 PUMA、Bax 及 Bcl-2蛋白錶達水平採用 Western blot 方法檢測。結果與 Control 組比較:PUMA 組、DDP 組及 PUMA+DDP 組 A549細胞增殖均顯著降低(P <0.01),且 PUMA+DDP組降低程度最彊(P <0.01);凋亡率均顯著升高(P <0.01);Bax 蛋白水平呈顯著性升高(P <0.01),Bcl-2蛋白呈顯著性下降(P <0.01)。結論外源性 PUMA 可抑製肺癌 A549細胞增殖,促進凋亡,其機製與增加細胞 Bax 蛋白錶達,降低 Bcl-2蛋白錶達有關。
목적:탐토외원성 p53상조조망조제인자(PUMA)대비소세포폐암 A549세포증식、조망적영향。방법장폐암A549세포분위 Control 조、공재체조、PUMA 조(전염 pCEP4-(HA)2-PUMA 질립),DDP 조(10μg· mL-1)화 PUMA+DDP 조(전염 pCEP4-(HA)2-PUMA 질립,가10μg·mL-1순박)5개조。세포생존솔화조망솔분별용 MTT 법화류식세포의검측,세포 PUMA、Bax 급 Bcl-2단백표체수평채용 Western blot 방법검측。결과여 Control 조비교:PUMA 조、DDP 조급 PUMA+DDP 조 A549세포증식균현저강저(P <0.01),차 PUMA+DDP조강저정도최강(P <0.01);조망솔균현저승고(P <0.01);Bax 단백수평정현저성승고(P <0.01),Bcl-2단백정현저성하강(P <0.01)。결론외원성 PUMA 가억제폐암 A549세포증식,촉진조망,기궤제여증가세포 Bax 단백표체,강저 Bcl-2단백표체유관。
ABSTRACT:Objective To investigate the effects of exogenous p53 up-regulated modulator of apoptosis(PUMA)on the proliferation and apoptosis of non-small cell lung cancer A549 cells. Methods Non-small cell lung cancer A549 cells were divided into 5 groups:control group,empty vector group,PUMA group(cells were transfected with pCEP4-(HA)2-PUMA plasmids),DDP group(cells were treated with 10 μg·mL-1 cisplatin),and PUMA+DDPgroup(cells were trans-fected with pCEP4-(HA)2-PUMA plasmids and treated with 10 μg·mL-1 cisplatin).Cell growth and apoptosis were determined by MTT assay and flow cytometry,respectively.The expression of PUMA,Bax and Bcl-2 proteins were detected by Western blot.Results Compared with control group,the proliferation of A549 cells was decreased and the apoptosis of A549 cells was increased in PUMA,DDP and PUMA+DDP groups(P <0.01).Maximum decrease in cell proliferation was observed in PUMA+DDP group(P <0.01).In addition,compared with control group,Bax pro-tein expression was up-regulated and Bcl-2 protein expression was down-regulated in PUMA, DDP and PUMA+DDP groups(P <0.01).Conclusion Exogenous PUMA can inhibit prolifera-tion and promote apoptosis through increasing Bax expression and decreasing Bcl-2 expression in non-small cell lung cancer A549 cells.