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文殊兰叶氯仿提取物诱导NCI-H460细胞凋亡的研究[J]. 肿瘤防治研究, 2011, 38(06): 628-631. DOI: 10.3971/j.issn.1000-8578.2011.06.005
引用本文: 文殊兰叶氯仿提取物诱导NCI-H460细胞凋亡的研究[J]. 肿瘤防治研究, 2011, 38(06): 628-631. DOI: 10.3971/j.issn.1000-8578.2011.06.005
Study on Apoptosis of NCI-H460 Cells Induced by Chloroform Extract of Leaves from Crinum Asiaticum[J]. Cancer Research on Prevention and Treatment, 2011, 38(06): 628-631. DOI: 10.3971/j.issn.1000-8578.2011.06.005
Citation: Study on Apoptosis of NCI-H460 Cells Induced by Chloroform Extract of Leaves from Crinum Asiaticum[J]. Cancer Research on Prevention and Treatment, 2011, 38(06): 628-631. DOI: 10.3971/j.issn.1000-8578.2011.06.005

文殊兰叶氯仿提取物诱导NCI-H460细胞凋亡的研究

Study on Apoptosis of NCI-H460 Cells Induced by Chloroform Extract of Leaves from Crinum Asiaticum

  • 摘要: 目的研究文殊兰叶氯仿提取物(CE)对非小细胞肺癌NCI-H460细胞增殖和凋亡的影响。方法通过MTT法检测CE对NCI-H460细胞的生长抑制作用;采用Hoechst 33258荧光染色法检测CE作用后凋亡细胞形态的变化;通过免疫细胞化学检测细胞凋亡相关蛋白Bcl-2和Bax的表达;采用流式细胞术(FCM)检测CE作用后对细胞周期的影响。结果CE抑制NCI-H460细胞增殖,其24、48、72 h的IC50分别为:(36.22 ±3.04)、(41.21±2.50)、(62.55±3.47) mg/L;荧光染色显示,经CE作用后的细胞出现细胞核裂解,染色质浓缩,产生凋亡小体;免疫细胞化学法显示CE能增强促进凋亡蛋白Bax和降低抑制凋亡蛋白Bcl-2的表达;FCM检测表明CE作用后的细胞被阻滞在G1/S期。结论CE在体外能有效地抑制NCI-H460细胞生长,其机制可能与改变细胞周期并诱导细胞凋亡有关。

     

    Abstract: ObjectiveTo investigate the effect of chloroform extracts (CE) of leaves from Crinum asiaticum on proliferation and apoptosis of non-small cell lung cancer(NSCLC) NCI-H460 cells . Methods The activity of cell growth inhibition of NCI-H460 cells was measured by MTT assay. Morphological changes of cell nuclei were observed by Hoechst 33258 staining. The expression levels of Bcl-2 and Bax proteins were examined by immunocytochemistry staining. Flow cytometry was performed to measure the cell cycle. ResultsCE displayed growth inhibitory activity against NCI-H460 cells with IC50 values of 36.22 ±3.04, 41.21±2.50 and 62.55±3.47 mg/L for 24,48 and 72 h, respectively. The effect enhanced with an increase in the concentration of CE. The condensed chromatin, nuclear fragmentation and a large number of apoptotic bodies was observed by Hoechst 33258 staining. The percentage of apoptosis in NCI-H460 cells increased after treated with CE, compared with control. The expression level of Bax protein in NCI-H460 cells cultured with CE were higher than that of control, and the expression level of Bcl-2 protein in NCI-H460 cells dealt with CE were lower than that of control. The arrest of NCI-H460 cells in G1/S phases was induced by CE. ConclusionIn vitro CE significantly inhibited the growth of NCI-H460 cells. Antitumor mechanism of NCI-H460 cells may be associated with the changes of cell cycle and cell apoptosis.

     

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