Zhou Rui-qing, Gong Yu-ping, Zheng Bo-hui, Yang Xi
Department of Hematology and Research Lab of Hematology, West China Hospital, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2010 Sep;41(5):789-92.
To assess effects of proteasome inhibitor Bortezomib (Bor) in combination with Daunorubicin (DNR) on proliferation, apoptosis and the expression of Bcl-2 mRNA in primary leukemia cells in vitro.
Primary leukemia cells were isolated from bone marrow of adult acute leukemia patients using Ficoll liquid, then the primary leukemia cells were treated with different concentration of these two drugs (Bor 5, 10, 20, 50 nmol/L, DNR 50, 100, 200, 500 nmol/L, and Bor 5, 10 nmol/L combined with DNR 50, 100, 200, 500 nmol/L respectively ). Cells proliferation, IC50 and CDI were analyzed by MTT assay, cellular apoptosis was observed by flow cytometry, Bcl-2 mRNA was analyzed by RT-PCR.
Growth inhibition ratio of all the types of acute leukemia cells were increased with the treatment of DNR and Bor in dose-dependent manner. Combined with Bor (5, 10 nmol/L),the IC50 of DNR decreased from (102 +/- 27) nmol/L to (73 +/- 26), (55 +/- 22) nmol/L respectively. DNR 200 nmol/L combined with Bor 10 nmol/L showed a better synergism (CDI = 0. 17). Compared with control group and single drug (DNR or Bor) group, there were obvious increase of apoptosis ratio and obvious decrease of Bcl-2 in the group of DNR 100 nmol/L combined with Bor 20 nmol/L after 24 h or 48 h cultivation (P < 0.05).
Bor combined with DNR shows synergetic effect in promoting the apoptosis of adult acute leukemia primary cells as well as inhibitory effect on the proliferation of leukemia cells.
评估蛋白酶体抑制剂硼替佐米(Bor)联合柔红霉素(DNR)对原代白血病细胞体外增殖、凋亡及Bcl-2 mRNA表达的影响。
采用Ficoll液从成年急性白血病患者骨髓中分离原代白血病细胞,然后用不同浓度的这两种药物(Bor 5、10、20、50 nmol/L,DNR 50、100、200、500 nmol/L,以及Bor 5、10 nmol/L分别与DNR 50、100、200、500 nmol/L联合)处理原代白血病细胞。通过MTT法分析细胞增殖、IC50和CDI,通过流式细胞术观察细胞凋亡,通过RT-PCR分析Bcl-2 mRNA。
所有类型急性白血病细胞的生长抑制率随DNR和Bor处理呈剂量依赖性增加。与Bor(5、10 nmol/L)联合时,DNR的IC50分别从(102±27)nmol/L降至(73±26)、(55±22)nmol/L。DNR 200 nmol/L与Bor 10 nmol/L联合显示出更好的协同作用(CDI = 0.17)。与对照组和单药(DNR或Bor)组相比,培养24 h或48 h后,DNR 100 nmol/L与Bor 20 nmol/L联合组的凋亡率明显增加,Bcl-2明显降低(P < 0.05)。
Bor联合DNR在促进成年急性白血病原代细胞凋亡以及抑制白血病细胞增殖方面显示出协同作用。