Kobylinska Agnieszka, Blonski Jerzy Z, Hanausek Malgorzata, Walaszek Zbigniew, Robak Tadeusz, Kilianska Zofia M
Department of Cytobiochemistry, University of Lodz, 90-237 Lodz, Poland.
Oncol Rep. 2004 Mar;11(3):699-705.
The present study investigated a correlation between expression of Bcl-2 family members, Bax and Bcl-2 (the Bax/Bcl-2 ratio values) in B-CLL cells in vivo and the response of these cells to chemotherapy. Western blot technique combined with videodensitometry was used for Bax and Bcl-2 determination in homogenate, nuclear and postnuclear fractions of mononuclear cells isolated from peripheral blood of B-CLL patients treated with cladribine alone (C), and in combination with cyclophosphamide (CC) or mitoxantrone and cyclophosphamide (CMC). The Bax/Bcl-2 ratio values were changed in B-CLL cells originated from blood samples of patients treated by the three therapy protocols, and was the most elevated in the case of CMC treatment. High degree of B-CLL cell apoptosis induction with cladribine combined with mitoxantrone and cyclophosphamide was confirmed by DNA fragmentation and an appearance of apoptotic morphology among leukemic cells from the blood of patients treated with this form of combined therapy.
本研究调查了体内B细胞慢性淋巴细胞白血病(B-CLL)细胞中Bcl-2家族成员Bax和Bcl-2的表达(Bax/Bcl-2比值)与这些细胞对化疗反应之间的相关性。采用蛋白质免疫印迹技术结合图像密度测定法,对单独使用克拉屈滨(C)、联合环磷酰胺(CC)或米托蒽醌与环磷酰胺(CMC)治疗的B-CLL患者外周血中分离的单核细胞匀浆、细胞核及核后部分中的Bax和Bcl-2进行测定。三种治疗方案治疗患者血样来源的B-CLL细胞中Bax/Bcl-2比值发生了变化,其中CMC治疗时该比值升高最为明显。DNA片段化以及接受这种联合治疗形式的患者血液中白血病细胞出现凋亡形态,证实了克拉屈滨联合米托蒽醌和环磷酰胺可高度诱导B-CLL细胞凋亡。