首页> 外文期刊>Journal of Cancer Research and Therapeutics >Synergistic induction of apoptosis in B-cell chronic lymphocytic leukemia cells after treatment with all-trans retinoic acid in combination with interleukin-21 and rituximab
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Synergistic induction of apoptosis in B-cell chronic lymphocytic leukemia cells after treatment with all-trans retinoic acid in combination with interleukin-21 and rituximab

机译:全反式维甲酸联合白介素-21和利妥昔单抗治疗后协同诱导B细胞慢性淋巴细胞白血病细胞凋亡

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Aim: B-cell chronic lymphocytic leukemia (B-CLL) is the most common adult leukemia in the Western world and characterized by the progressive expansion of malignant B lymphocytes in peripheral blood. In spite of advances in sciences to recognize the number of effective agents for the treatment of chronic lymphocytic leukemia (CLL), this leukemia is thought as incurable one. Introducing a new therapy that has a direct effect on B-CLL lymphocytes and no cytotoxic effects on the other cells is a great wish. Materials and Methods: Twenty-one patients with B-CLL were enrolled in the study. Peripheral blood mononuclear cells (PBMCs) were isolated from patients' blood samples and were further treated with all-tans retinoic acid (ATRA), interleukin (IL-21), and rituximab at concentrations of 30 ng/ml, 25 ng/ml, and 4 μg/ml, respectively. ATRA, IL21, and rituximab were used alone or in various combinations and their effects on apoptosis were measured using annexin V-fluorescein isothiocyanate apoptosis detection kit. Result: Treatment of the patients' cells with IL21 and rituximab showed a synergistic effect on the induction of apoptosis, in comparison with untreated CLL cells (P P Conclusion: Treatment of patients' PBMCs by ATRA in combination with IL21 and rituximab and also IL21 in combination with rituximab showed synergistic induction of apoptosis compared to untreated CLL cells as a negative control (P < 0.01). It seems that ATRA in combination with IL21 and rituximab activate different pathways of apoptosis (extrinsic pathway, intrinsic pathway, and granzyme B pathway).
机译:目的:B细胞慢性淋巴细胞性白血病(B-CLL)是西方世界最常见的成人白血病,其特征是外周血中恶性B淋巴细胞逐渐扩增。尽管科学界认识到用于治疗慢性淋巴细胞性白血病(CLL)的有效药物的数量不断提高,但这种白血病仍被认为是无法治愈的。引入一种对B-CLL淋巴细胞具有直接作用而对其他细胞无细胞毒性作用的新疗法是一个很大的愿望。材料与方法:21例B-CLL患者入选本研究。从患者的血液样本中分离出外周血单个核细胞(PBMC),并分别以浓度为30 ng / ml,25 ng / ml的全鞣维甲酸(ATRA),白介素(IL-21)和利妥昔单抗对其进行处理,和4μg/ ml。 ATRA,IL21和利妥昔单抗单独使用或以多种组合使用,并使用膜联蛋白V-荧光素异硫氰酸酯凋亡检测试剂盒测量它们对凋亡的影响。结果:与未处理的CLL细胞相比,用IL21和利妥昔单抗治疗患者的细胞显示出诱导凋亡的协同作用(PP结论:ATRA联合IL21和利妥昔单抗以及IL21联合治疗患者的PBMC与未处理的CLL细胞相比,与利妥昔单抗联合显示出协同的凋亡诱导作用(P <0.01),似乎ATRA与IL21和利妥昔单抗联合激活了不同的凋亡途径(外源途径,内在途径和粒酶B途径)。

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