论文部分内容阅读
目的研究抗凋亡基因bcl-2在46例急性白血病骨髓细胞中的表达及其与凋亡、细胞增殖、DNA倍体及疗效间关系的临床意义。方法采用免疫流式细胞术。结果46例急性白血病细胞均不等程度表达bcl-2染色阳性率8.3%~47.7%和凋亡细胞3.0%~21%。bcl-2高表达者13例(≥20%),低表达者33例(<20%)。多数病例的bcl-2表达与凋亡呈负相关,高bcl-2低凋亡(<15%)11例(84.6%),低bcl-2高凋亡(≥15%)者19例(57.6%),两者均低14例(42.2%),两者均高2例。与bcl-2低表达者比较,bcl-2高表达者完全缓解率低(6/13例,46.1%比29/33例,87.9%),DNA异倍体者多(11/13例,84.6%比8/33例,24.2%),且易复发(3/6例,50%比2/29例,6.8%)。结论由于bcl-2表达的异质性,bcl-2不是调控凋亡的唯一因素,但有临床预后意义,也可能在白血病发生上起作用
Objective To investigate the expression of anti-apoptotic gene bcl-2 in 46 acute leukemia myeloid cells and its relationship with apoptosis, cell proliferation, DNA ploidy and clinical efficacy. Methods using immune flow cytometry. Results The positive rate of bcl-2 staining was 8.3% to 47.7% and the apoptotic cells were 3.0% to 21%. There were 13 cases (≥20%) with high bcl-2 expression and 33 cases (<20%) with low expression. In most cases, bcl-2 expression was negatively correlated with apoptosis, with high bcl-2 low apoptosis (<15%) in 11 cases (84.6%), and low bcl-2 high apoptosis (≥15%) in 19 cases. (57.6%), both were 14 cases (42.2%) lower, both of which were 2 cases high. Compared with those with low expression of bcl-2, the complete response rate of patients with high bcl-2 expression was low (6/13 cases, 46.1% vs 29/33 cases, 87.9%), and DNA aneuploidy was much more (11/ 13 cases, 84.6% compared with 8/33 cases, 24.2%), and easy to relapse (3/6 cases, 50% than 2/29 cases, 6.8%). Conclusion Because of the heterogeneity of bcl-2 expression, bcl-2 is not the only factor regulating apoptosis, but it has clinical prognostic significance and may also play a role in the development of leukemia.