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机构地区:[1]湖北省医学会,武汉430064 [2]华中科技大学同济医学院附属协和医院骨科 [3]湖北省十堰市妇幼保健院 [4]孝感市中心医院骨科
出 处:《中华实验外科杂志》2009年第9期1195-1197,共3页Chinese Journal of Experimental Surgery
摘 要:目的观察多肽RGDS—GG—KLAKLAKK对体外培养人骨肉瘤细胞MG-63生长的影响,并探讨其作用机制。方法将不同浓度(0、25、50、75、100umol/L)多肽RGDS—GG—KLAKLAKK与MG-63细胞混合培养,用噻唑蓝(MYr)比色法测量多肽RGDS—GG—KLAKLAKK对MG-63细胞生长的抑制作用,流式细胞术(FCM)检测多肽RGDS—GG—KLAKLAKK作用于MG-63细胞后的凋亡率,逆转录一聚合酶链反应(1it—PCR)测量MG-63细胞Survivin mRNA水平的变化。结果多肽RGDS—GG—KLAKLAKK明显抑制MG-63细胞的增殖,并有时间和剂量依赖性,在24、48h的IC50分别为46.8、37.6umol/L(P〈0.05)。多肽RGDS—GG—KLAKLAKK随着剂量的增加MG-63细胞的凋亡率从5.23%上升至38.90%(P〈0.01)。MG-63细胞在多肽RGDS—GG—KLAKLAKK处理后,Survivin mRNA的表达出现明显下降。结论多肽RGDS-GG-KLAKLAKK能够抑制人骨肉瘤MG-63细胞的增殖,并诱导其凋亡。Objective To investigate the effects of the peptides (RGDS-GG-KLAKLAKK) on the growth of human osteosarcoma cells (MG-63). Methods The MG-63 cells were co-cultured with different concentrations of RGDS-GG-KLAKLAKK ( 0,25,50,75,100 umol/L). The suppressive effect of RGDS-GG-KLAKLAKK on MG-63 cells was examined by MTT assay. The apoptosis of MG-63 cells was observed by flow cytometry ( FCM ). The Survivin mRNA levels were detected by RT-PCR. Results RGDS-GG-KLAKLAKK obviously suppressed the proliferation of MG-63 cells in both time-and dose-dependent manners, and the IC50 was 46.8,37.6umol/L at 24 and 48 h respectively ( P 〈 0.05). The FCM results indicated that apoptosis ratio of MG-63 cells was increased from 5.23% of untreated cells to 38. 90% of treated cells (P 〈 0.01 ). RT-PCR revealed that the expression of Survivin mRNA in MG-63 cells was down-regulated. Conclusion The RGDS-GG-KLAKLAKK can suppress the proliferation of MG-63 cells,and induce their apoptosis.
分 类 号:R738.1[医药卫生—肿瘤] R737.310.2[医药卫生—临床医学]
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