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出 处:《实用癌症杂志》2006年第3期244-246,253,共4页The Practical Journal of Cancer
摘 要:目的探讨HA14-1对白血病细胞的作用及其与Bcl-2、Bcl-xL和Bax的关系。方法不同浓度HA14-1(25,50,75,100μmol/L)作用于U937、BALL-1和Jurkat clone E6-1细胞4 h,在流式细胞仪上检测作用前后Bcl-2、Bax、Bcl-xL的平均荧光指数(MFI)及作用后细胞凋亡情况。结果①随HA14-1剂量的增加,存活细胞逐渐减少,U937从(93.7±1.5)%降至(14.8±1.9)%;Jurkat clone E6-1从(94.7±1.5)%降至(12.4±1.3)%;BALL-1从(94.7±0.8)%降至(0.9±0.6)%。同一HA14-1剂量时,不同细胞的存活率与Bcl-2表达高低呈负相关,有非常显著性差异(P<0.01)。②随剂量的增加细胞凋亡率逐渐增加,如Jurkatclone E6-1凋亡率从(0.5±0.1)%上升至(60.1±2.6)%;在较高剂量时(100μmol/L),细胞大幅度坏死,坏死率从<(3.3±0.6)%增至(26.8±1.6)%。③HA14-1作用引起3种细胞中Bcl-2表达下降,而HA14-1作用前后Bcl-xL和Bax在3种细胞中均无显著改变。结论HA14-1可以诱导不同Bcl-2表达水平的白血病细胞凋亡,并且细胞对HA14-1的敏感与细胞中Bcl-2表达水平呈相反关系,这为临床逆转Bcl-2高表达造成的化疗耐药提供了理论基础。Objective To investigate the effects of HA14-1 on leukemic cells and the relationship between the effects and the level of Bcl-2、Bcl-xL and Bax in these cells. Methods The leukemic cell lines of U937、BALL-1 and Jurkat clone E6-1 were co- cultured with different concentrations of HA14-1 (25,50,75,100 μmol/L) for 4 hours. The mean fluorescent index (MFI) and the apoptosis of Bcl-2、Bax 、Bcl-xL were detected with the FCM before and after the treatment of HA14-1. Results ①With the increase of concentration of HA14-1, the viability of the cells were decreased from (93.7 ± 1.5) % to ( 14.8 ± 1.9) % in U937 cell; from(94.7± 1.5)% to(12.4 ± 1.3)% in Jurkat clone E6-1; from (94.7 ± 0.8)% to(0.9 ± 0.6)% in BALL-1. With the same HA14-1 concentration, the viability of different cells lines were negatively related with the Bcl-2 level. ②With the increase of HA14- 1 concentration, apoptosis rate increased gradually, such as from(0.5 ± 1.0)% to (60.1 ± 2.6)% in Jurkat clone E6-1. With the high concentration(100 μmol/L) of HA14-1, extreme necrosis was observed . The cell necrotic rate increased from less than(3.3 ± 0.6) % to(26.7 ± 1.6)%. OWith the treatment of HA14-1 ,the Bcl-2 was markedly decreased in all three cells, but the Bcl-xL and Bax were not changed significantly. Conclusion HA14-1 can induce apoptosis of leukemia cells with different Bel-2 level,and the sensitivity of leukemia cells to HA14-1 is opposite to their Bcl-2 expression level ,that is cell with high Bcl-2 level is more sensitive to HA14-1,which offers theoretical basis for reversing MDR clinically.
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