现代泌尿外科杂志
現代泌尿外科雜誌
현대비뇨외과잡지
Journal of Modern Urology
2015年
11期
808-812
,共5页
徐烈雨%廉建坡%陈东宁%祝宇%赵菊平%吴瑜璇%沈周俊%宁光
徐烈雨%廉建坡%陳東寧%祝宇%趙菊平%吳瑜璇%瀋週俊%寧光
서렬우%렴건파%진동저%축우%조국평%오유선%침주준%저광
表皮生长因子受体%埃罗替尼%肾上腺皮质癌%增殖%凋亡
錶皮生長因子受體%埃囉替尼%腎上腺皮質癌%增殖%凋亡
표피생장인자수체%애라체니%신상선피질암%증식%조망
epidermal growth factor receptor%Erlotinib%adrenocortical carcinoma%proliferation%apoptosis
目的:体外探讨EGFR抑制剂埃罗替尼(Erlotinib)对肾上腺皮质癌SW13细胞的增殖、凋亡及细胞周期的影响。方法应用M T T试验观察埃罗替尼对SW13细胞系的生长抑制作用;流式细胞实验检测其对肾上腺皮质癌细胞系凋亡及细胞周期的影响;Western blot检测埃罗替尼对EGFR下游信号通路蛋白的影响,进一步阐明其作用机制。结果埃罗替尼呈剂量‐时间相关地抑制SW13细胞增殖,药物作用24 h时IC50为20.51μmol/L ;埃罗替尼可以诱导SW13细胞凋亡,处理24 h后,空白组早期凋亡率为(1.62±0.21)%,20μmol/L埃罗替尼治疗组为(13.49±0.48)%,存在统计学差异(P<0.05);而埃罗替尼对SW13细胞周期分布无影响。埃罗替尼下调p‐ERK蛋白表达水平,但不影响p‐mTOR表达水平。结论埃罗替尼可以抑制SW13细胞增殖,其作用机制可能与促进凋亡、抑制ERK信号通路有关。
目的:體外探討EGFR抑製劑埃囉替尼(Erlotinib)對腎上腺皮質癌SW13細胞的增殖、凋亡及細胞週期的影響。方法應用M T T試驗觀察埃囉替尼對SW13細胞繫的生長抑製作用;流式細胞實驗檢測其對腎上腺皮質癌細胞繫凋亡及細胞週期的影響;Western blot檢測埃囉替尼對EGFR下遊信號通路蛋白的影響,進一步闡明其作用機製。結果埃囉替尼呈劑量‐時間相關地抑製SW13細胞增殖,藥物作用24 h時IC50為20.51μmol/L ;埃囉替尼可以誘導SW13細胞凋亡,處理24 h後,空白組早期凋亡率為(1.62±0.21)%,20μmol/L埃囉替尼治療組為(13.49±0.48)%,存在統計學差異(P<0.05);而埃囉替尼對SW13細胞週期分佈無影響。埃囉替尼下調p‐ERK蛋白錶達水平,但不影響p‐mTOR錶達水平。結論埃囉替尼可以抑製SW13細胞增殖,其作用機製可能與促進凋亡、抑製ERK信號通路有關。
목적:체외탐토EGFR억제제애라체니(Erlotinib)대신상선피질암SW13세포적증식、조망급세포주기적영향。방법응용M T T시험관찰애라체니대SW13세포계적생장억제작용;류식세포실험검측기대신상선피질암세포계조망급세포주기적영향;Western blot검측애라체니대EGFR하유신호통로단백적영향,진일보천명기작용궤제。결과애라체니정제량‐시간상관지억제SW13세포증식,약물작용24 h시IC50위20.51μmol/L ;애라체니가이유도SW13세포조망,처리24 h후,공백조조기조망솔위(1.62±0.21)%,20μmol/L애라체니치료조위(13.49±0.48)%,존재통계학차이(P<0.05);이애라체니대SW13세포주기분포무영향。애라체니하조p‐ERK단백표체수평,단불영향p‐mTOR표체수평。결론애라체니가이억제SW13세포증식,기작용궤제가능여촉진조망、억제ERK신호통로유관。
ABSTRACT:Objective To investigate the effect and mechanism of epidermal growth factor receptor (EGFR) inhibitor Er‐lotinib on human adrenocortical carcinoma cell line SW13 in vitro .Methods The proliferation of SW13 after exposure to Er‐lotinib was detected with MTT assay .The apoptosis and cell cycle was determined with Annex‐VI and flow cytometry .The ex‐pression of proteins associated with EGFR signaling were examined with Western blot .Results Erlotinib inhibited SW13 cell proliferation in a dose‐and time‐dependent manner in vitro .The IC50 after exposure of 24 h was 20 .51 μmol/L .Erlotinib in‐duced apoptosis ,cell apoptosis rate in erlotinib 20μmol/L group 24 h was (13 .49 ± 0 .48)% ,significantly higher than that in the control group (1 .62 ± 0 .21)% .Erlotinib had no effect on cell cycle .The expression of p‐ERK was down regulated ,while the expression of p‐mTOR was not affected .Conclusions The proliferation of SW13 cells could be inhibited by Erlotinib , and possible mechanisms involved up‐regulated apoptosis and down‐regulated ERK signaling pathway .