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缺乏促凋亡 BAX 的淋巴瘤细胞对靶向抗凋亡 MCL-1 的 BH3 模拟物具有高度耐药性,但对传统的 DNA 损伤药物仍然敏感。

Lymphoma cells lacking pro-apoptotic BAX are highly resistant to BH3-mimetics targeting pro-survival MCL-1 but retain sensitivity to conventional DNA-damaging drugs.

机构信息

The Walter and Eliza Hall Institute of Medical Research, Melbourne, VIC, Australia.

Department of Medical Biology, University of Melbourne, Melbourne, VIC, Australia.

出版信息

Cell Death Differ. 2023 Apr;30(4):1005-1017. doi: 10.1038/s41418-023-01117-0. Epub 2023 Feb 8.

Abstract

BH3-mimetic drugs are an anti-cancer therapy that can induce apoptosis in malignant cells by directly binding and inhibiting pro-survival proteins of the BCL-2 family. The BH3-mimetic drug venetoclax, which targets BCL-2, has been approved for the treatment of chronic lymphocytic leukaemia and acute myeloid leukaemia by regulatory authorities worldwide. However, while most patients initially respond well, resistance and relapse while on this drug is an emerging and critical issue in the clinic. Though some studies have begun uncovering the factors involved in resistance to BCL-2-targeting BH3-mimetic drugs, little focus has been applied to pre-emptively tackle resistance for the next generation of BH3-mimetic drugs targeting MCL-1, which are now in clinical trials for diverse blood cancers. Therefore, using pre-clinical mouse and human models of aggressive lymphoma, we sought to predict factors likely to contribute to the development of resistance in patients receiving MCL-1-targeting BH3-mimetic drugs. First, we performed multiple whole genome CRISPR/Cas9 KO screens and identified that loss of the pro-apoptotic effector protein BAX, but not its close relative BAK, could confer resistance to MCL-1-targeting BH3-mimetic drugs in both short-term and long-term treatment regimens, even in lymphoma cells lacking the tumour suppressor TRP53. Furthermore, we found that mouse Eµ-Myc lymphoma cells selected for loss of BAX, as well as upregulation of the untargeted pro-survival BCL-2 family proteins BCL-XL and A1, when made naturally resistant to MCL-1 inhibitors by culturing them in increasing doses of drug over time, a situation mimicking the clinical application of these drugs. Finally, we identified therapeutic approaches which could overcome these two methods of resistance: the use of chemotherapeutic drugs or combined BH3-mimetic treatment, respectively. Collectively, these results uncover some key factors likely to cause resistance to MCL-1 inhibition in the clinic and suggest rational therapeutic strategies to overcome resistance that should be investigated further.

摘要

BH3 模拟药物是一种抗癌疗法,通过直接结合并抑制 BCL-2 家族的生存蛋白,可诱导恶性细胞凋亡。BH3 模拟药物 venetoclax 靶向 BCL-2,已被全球监管机构批准用于治疗慢性淋巴细胞白血病和急性髓细胞白血病。然而,虽然大多数患者最初反应良好,但在使用该药时出现耐药和复发是临床中的一个新出现的关键问题。尽管一些研究已经开始揭示涉及 BCL-2 靶向 BH3 模拟药物耐药的因素,但对于针对 MCL-1 的下一代 BH3 模拟药物,用于预防耐药的研究还很少,目前这些药物正在针对多种血液癌症进行临床试验。因此,我们使用侵袭性淋巴瘤的临床前小鼠和人类模型,试图预测接受 MCL-1 靶向 BH3 模拟药物治疗的患者中可能导致耐药性发展的因素。首先,我们进行了多次全基因组 CRISPR/Cas9 KO 筛选,发现促凋亡效应蛋白 BAX 的缺失,但不是其近亲 BAK 的缺失,可以赋予对 MCL-1 靶向 BH3 模拟药物的耐药性,无论是在短期还是长期治疗方案中,即使在缺乏肿瘤抑制因子 TRP53 的淋巴瘤细胞中也是如此。此外,我们发现,当使自然对 MCL-1 抑制剂耐药的小鼠 Eµ-Myc 淋巴瘤细胞通过随着时间的推移在增加剂量的药物中培养时,BAX 缺失以及非靶向生存 BCL-2 家族蛋白 BCL-XL 和 A1 的上调,选择了失去 BAX,以及上调非靶向生存 BCL-2 家族蛋白 BCL-XL 和 A1,这种情况模拟了这些药物的临床应用。最后,我们确定了克服这两种耐药方法的治疗方法:分别使用化疗药物或联合 BH3 模拟药物治疗。总之,这些结果揭示了一些在临床上可能导致 MCL-1 抑制耐药的关键因素,并提出了克服耐药的合理治疗策略,这些策略应该进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74fc/10070326/e5be0be4fb30/41418_2023_1117_Fig1_HTML.jpg

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