邓婉萍, 李永辉, 孙君重. 佛波酯类对白血病细胞的生物学作用[J]. 解放军医学院学报, 2016, 37(7): 798-803. DOI: 10.3969/j.issn.2095-5227.2016.07.033
引用本文: 邓婉萍, 李永辉, 孙君重. 佛波酯类对白血病细胞的生物学作用[J]. 解放军医学院学报, 2016, 37(7): 798-803. DOI: 10.3969/j.issn.2095-5227.2016.07.033
DENG Wanping, LI Yonghui, SUN Junzhong. Biological effects of phorbol esters on human leukemia cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(7): 798-803. DOI: 10.3969/j.issn.2095-5227.2016.07.033
Citation: DENG Wanping, LI Yonghui, SUN Junzhong. Biological effects of phorbol esters on human leukemia cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(7): 798-803. DOI: 10.3969/j.issn.2095-5227.2016.07.033

佛波酯类对白血病细胞的生物学作用

Biological effects of phorbol esters on human leukemia cells

  • 摘要: 目的 研究佛波酯类化合物12-O-十四烷酰佛波酯-13-乙酸酯(12-o-tetradecanoylophorbol-13-acetate,TPA)及其类似物TPD、MBPD、APD对人白血病细胞HL-60、Kasumi-1、U937、U937A/E、K562及K562/AO2细胞的增殖和凋亡作用,并探讨其可能的生物学机制。 方法 分别用(5 nmol/L、10 nmol/L、20 nmol/L、50 nmol/L)TPA、TPD、MBPD、APD作用于HL-60、Kasumi-1、U937、U937A/E、K562及K562/AO2细胞(由K562阿霉素诱导而来的多耐药细胞),应用CCK-8法检测细胞增殖抑制率,流式细胞术检测细胞凋亡情况。 结果 TPA、TPD、MBPD、APD均可抑制HL-60、Kasumi-1、U937、U937A/E、K562及K562/AO2细胞增殖,72 h的细胞抑制率分别为70%、50%、80%、80%、75%及50%,药物之间无明显差异。同时,上述药物可促进这些细胞的凋亡,且对AML1/ETO融合基因阴性的细胞作用更好(P< 0.05)。 结论 TPA及其衍生物TPD、MBPD及APD均可用于白血病的治疗,且AML1/ETO融合基因可能抑制佛波酯类药物对白血病细胞的作用。

     

    Abstract: Objective To investigate the effects of phorbol esters 12-o-tetradecanoylophorbol-13-acetate (TPA), TPD, MBPD and APD on apoptosis and proliferation of human leukemia cell lines HL-60, Kasumi-1, U937, U937A/E, K562 and K562/AO2 cells, and its possible mechanisms. Methods HL-60, Kasumi-1, U937, U937A/E, K562 and K562/AO2 cells were treated with (5 nmol/ L, 10 nmol/L, 20 nmol/L, 50 nmol/L) TPA, TPD, MBPD and APD, respectively. CCK-8 was used to detect the inhibition rate of cell proliferation, and flow cytometry was used to detect the apoptosis. Results TPA, TPD, MBPD, APD could inhibit the proliferation of HL-60, Kasumi-1, U937, U937A/E, K562 and K562/AO2 with the 72 h inhibition rate of 70%, 50%, 80%, 80%, 75% and 50%, respectively, and no significant difference was found between different drugs. In addition, they could promote the apoptosis of HL-60, Kasumi-1, U937, U937A/E, K562 and K562/AO2, especially for the AML1/ETO fusion genes negative cells (P< 0.05). Conclusion TPA, and its derivatives-TPD, MBPD and APD can be used in the treatment of leukemia, and AML1/ETO fusion gene may inhibit the effect of phorbol esters on leukemia cells.

     

/

返回文章
返回