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纸质出版:2012
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谢燕,喻秀丽,童立纺.硼替佐米对A549细胞增殖及p21、p27表达的影响[J].陆军军医大学学报(原第三军医大学学报),2012,34(17):1775-1778.
Xie Yan,Yu Xiuli,Tong Lifang.Anti-proliferation effect of proteasome inhibitor bortezomib in human lung adenocarcinoma A549 cells[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(17):1775-1778.
目的 研究蛋白酶体抑制剂硼替佐米对人肺癌A549细胞增殖、细胞周期及在体成瘤的影响。 方法 采用不同浓度的硼替佐米(0、100、200 nmol/L)作用于A549细胞4 h,观察其对蛋白酶体活性的影响。用硼替佐米(0、100、200 nmol/L)处理A549细胞48 h,采用MTT法、
3
H-TdR掺入法检测细胞增殖;流式细胞术PI染色检测细胞周期;Western blot检测p21、p27表达水平的变化;连续注射观察硼替佐米对裸鼠A549细胞移植瘤体积及质量的影响。 结果 硼替佐米可显著抑制A549细胞的蛋白酶体活性。MTT法、
3
H-TdR法检测显示,100 nmol/L处理组细胞较对照组增殖率分别降低24.5%、29.5%,200 nmol/L处理组进一步显著下降(P0.05);细胞周期分析显示,100、200 nmol/L处理组G
0
/G
1
期较对照组明显增加(P0.05)。Western blot检测显示,48 h时100、200 nmol/L处理组p21、p27蛋白表达较对照组明显增加,且呈浓度依赖(P0.05),48 h蛋白质水平高于24 h。连续注射硼替佐米后裸鼠移植瘤的质量抑制率达(36.0±12.4)%。 结论 硼替佐米可抑制A549细胞增殖,诱导细胞凋亡及发生G
0
/G
1
期阻滞,在体注射可抑制裸鼠成瘤,其抗肿瘤活性可能与抑制细胞周期蛋白p21、p27的降解有关。
Objective To investigate the effects of a proteasome inhibitor bortezomib on the proliferation
cell cycle and tumor formation of human lung adenocarcinoma A549 cells
and to explore the possible mechanisms involved. Methods Human lung adenocarcinoma A549 cells were cultured and treated with different concentrations of bortezomib (0
100 and 200 nmol/L) for 4 h
and the
proteasome activity were measured to confirm its inhibitory effects. The A549 cells were further treated with different concentrations of bortezomib (0
100 and 200 nmol/L) for 24-48 h. Cell proliferation was determined by MTT assay and
3
H-TdR absorption
respectively. Cell cycle was detected by flow cytometry
and the protein levels of p21 and p27 were determined by Western blotting. A549 cells were implanted subcutaneously into nude mice to establish the xenograft tumor models
and the xenograft tumor bearing mice were subjected to bortezomib. The tumor volume and weight in all groups were measured
and the tumor inhibitory rate was calculated. Results Bortezomib significantly inhibited the proteasome activity in A549 cells. The MTT and
3
H-TdR results showed that cell proliferation decreased by 24.5% and 29.5% in the 100 nmol/L bortezomib group
respectively
and a more significant decease was observed in the 200 nmol/L bortezomib group compared with the control group (P0.05). Cell cycle analysis showed that the number of cells at G
0
/G
1
phase was significantly increased in the 100 nmol/L and 200 nmol/L bortezomib groups compared with the control group (P0.05). Western blot results showed that p21 and p27 significantly increased in a dose-dependent manner in the 100 nmol/L and 200 nmol/L bortezomib groups compared with the control group (P0.05). In addition
the levels of p21 and p27 in the bortezomib group were significantly higher at 48 h than those at 24 h. After continuous injection
the weight of the xenograft tumors was reduced by (36.0±12.4)% in the bortezomib group compared with the control group. Conclusion Bortezomib can inhibit A549 cell proliferation and induce cell cycle arresting at G
0
/G
1
phase
probably by inhibiting the degradation of p21 and p27 proteins in A549 cells.
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