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作 者:周剑锋[1,2,3] 陈燕[1,2,3] 李崇渔[1,2,3] 刘文励 杨林花[1,2,3] 乔振华 周木想[1,2,3] 王辨明
机构地区:[1]同济医科大学附属协和医院血液科 [2]同济医科大学附属同济医院血液科 [3]山西医科大学第二附属医院血液科
出 处:《中华血液学杂志》1997年第11期584-587,共4页Chinese Journal of Hematology
基 金:国家教委留学回国人员课题
摘 要:目的:探讨急性髓系白血病(AML)细胞凋亡径路的特征及调控模式。方法:运用流式细胞仪(FACS)、DNA电泳、Northernblot分析技术,观察了化疗药物足叶乙甙(Vp16)作用于原代AML细胞前后,bcl-XL表达与凋亡的敏感性、临床特征、预后的关系。结果:绝大部分AML高表达bcl-XLmRNA病例经Vp16处理后,其bcl-XL虽然下调,但仍维持较高水平,并对凋亡诱导不敏感,与高白细胞数、髓外浸润等不良预后特征相关,化疗后不易缓解,处于长期缓解中的病例经Vp16处理后,bcl-XL亦表达下调,但凋亡率远低于AML细胞。结论:bcl-XL高表达与AML的发生、维持和化疗耐药性相关,bcl-XL高表达下调是凋亡启动的基础,但本身不足以引致凋亡。Objective:To investigate the characteristics and regulation of apoptosis in acute myeloid leukemic cells.Methods:Flow cytometry,DNA electrophoresis and Northern blot were used to analyze the expression of bclXL before and after Vp16 treatment,and the relationships between bclXL expression and apoptotic sensitivity, clinical features and prognosis were also analyzed.Results:Most of the leukemic cells from AML patients overexpressed bclXL mRNA.The expression of bclXL was still maintained high level after Vp16 treatment in patients with pretreatment overexpression.These patients were resistant to apoptosis,poor responsed to chemotherapy and associated with adverse prognostic features,such as high WBC counts,local leukemic infiltrations.Bone marrow cells from long term remission AML patients and normal controls also showed bclXL downregulation after in vitro Vp16 treatment,but the apoptotic rates were lower than that in nonremissive AML.Conclusion:Overexpression of bclXL played an important role in leukemogenesis and drug resistance.Downregulation of bclXL was necessary but not sufficient to initiate apoptosis.
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