PO.ET03.07 · 实验与分子治疗
Venetoclax耐药的AML细胞模型作为探索针对BCL2抑制剂耐药的新一代药物的平台
Venetoclax-resistant AML cell models as a platform for exploring new generation drug for BCL2 inhibitor resistance
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
BCL2是凋亡通路中的一个关键调控蛋白。Venetoclax(ABT-199)是一种口服生物利用度高且高度选择性的BCL-2抑制剂,与去甲基化药物(HMA)联合使用时在急性髓系白血病(AML)中显示出有前景的疗效,带来高缓解率和显著延长的总生存期。然而,相当数量的患者出现耐药或复发,凸显了需要新策略以克服获得性venetoclax耐药。为研究这一问题,我们通过对venetoclax逐步递增浓度(范围为1 nM至500 nM)的长期暴露,在三种AML细胞系(RS4;11、MOLM-13和MV4-11)中建立了venetoclax耐药模型。所得耐药细胞对venetoclax的敏感性显著降低,与其亲代细胞相比耐药水平超过160倍。这些模型可作为评估新型BCL-2抑制剂、联合治疗方案和其他靶向药物的宝贵平台。此外,它们为阐明venetoclax耐药的潜在机制提供了关键资源。
查看英文原文 English abstract
BCL2 is a key regulatory protein in the apoptotic pathway. Venetoclax (ABT-199), an orally bioavailable and highly selective BCL-2 inhibitor, has demonstrated promising efficacy in acute myeloid leukemia (AML) when used in combination with hypomethylating agents (HMA), leading to high remission rates and significantly prolonged overall survival. However, a considerable number of patients developed resistance or experienced relapse, highlighting the need for new strategies to overcome acquired venetoclax resistance. To investigate this issue, we established venetoclax-resistant models in three AML cell lines (RS4;11, MOLM-13, and MV 4-11) through prolonged exposure to progressively increasing concentrations of venetoclax (ranging from 1 nM to 500 nM). The resulting resistant cells exhibited a marked reduction in venetoclax sensitivity, with resistance levels exceeding 160-fold compared to their parental counterparts. These models serve as a valuable platform for evaluating novel BCL-2 inhibitors, combination treatment regimens, and other targeted agents. Moreover, they provide a crucial resource for elucidating the underlying mechanisms of venetoclax resistance.
利益披露 Disclosure
J. Wang,
BioDuro Employment.
J. Liu,
BioDuro Employment.
L. Teng,
BioDuro Employment.