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单细胞多组学揭示了允许 CLL 在 venetoclax 治疗期间复发的多层适应的规模。

Single-cell multiomics reveal the scale of multilayered adaptations enabling CLL relapse during venetoclax therapy.

机构信息

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

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

出版信息

Blood. 2022 Nov 17;140(20):2127-2141. doi: 10.1182/blood.2022016040.

Abstract

Venetoclax (VEN) inhibits the prosurvival protein BCL2 to induce apoptosis and is a standard therapy for chronic lymphocytic leukemia (CLL), delivering high complete remission rates and prolonged progression-free survival in relapsed CLL but with eventual loss of efficacy. A spectrum of subclonal genetic changes associated with VEN resistance has now been described. To fully understand clinical resistance to VEN, we combined single-cell short- and long-read RNA-sequencing to reveal the previously unappreciated scale of genetic and epigenetic changes underpinning acquired VEN resistance. These appear to be multilayered. One layer comprises changes in the BCL2 family of apoptosis regulators, especially the prosurvival family members. This includes previously described mutations in BCL2 and amplification of the MCL1 gene but is heterogeneous across and within individual patient leukemias. Changes in the proapoptotic genes are notably uncommon, except for single cases with subclonal losses of BAX or NOXA. Much more prominent was universal MCL1 gene upregulation. This was driven by an overlying layer of emergent NF-κB (nuclear factor kappa B) activation, which persisted in circulating cells during VEN therapy. We discovered that MCL1 could be a direct transcriptional target of NF-κB. Both the switch to alternative prosurvival factors and NF-κB activation largely dissipate following VEN discontinuation. Our studies reveal the extent of plasticity of CLL cells in their ability to evade VEN-induced apoptosis. Importantly, these findings pinpoint new approaches to circumvent VEN resistance and provide a specific biological justification for the strategy of VEN discontinuation once a maximal response is achieved rather than maintaining long-term selective pressure with the drug.

摘要

维奈托克(VEN)抑制生存蛋白 BCL2 以诱导细胞凋亡,是慢性淋巴细胞白血病(CLL)的标准治疗方法,在复发性 CLL 中可实现高完全缓解率和延长无进展生存期,但最终会失去疗效。现在已经描述了与 VEN 耐药相关的一系列亚克隆遗传变化。为了全面了解对 VEN 的临床耐药性,我们结合单细胞短读和长读 RNA 测序,揭示了以前未被重视的获得性 VEN 耐药性所依赖的遗传和表观遗传变化的规模。这些变化似乎是多层次的。一层包括凋亡调节剂 BCL2 家族的变化,特别是生存家族成员。这包括 BCL2 中的先前描述的突变和 MCL1 基因的扩增,但在个体患者白血病中是异质的。促凋亡基因的变化非常罕见,除了个别情况下 BAX 或 NOXA 的亚克隆缺失。更突出的是普遍的 MCL1 基因上调。这是由新兴 NF-κB(核因子 kappa B)激活的上层驱动的,在 VEN 治疗期间在循环细胞中持续存在。我们发现 MCL1 可以是 NF-κB 的直接转录靶标。替代生存因子的转换和 NF-κB 的激活在 VEN 停药后基本上消散。我们的研究揭示了 CLL 细胞逃避 VEN 诱导的细胞凋亡的能力的可塑性程度。重要的是,这些发现指出了克服 VEN 耐药的新方法,并为一旦达到最大反应就停止 VEN 而不是长期用药物维持选择性压力的策略提供了具体的生物学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2634/10653037/64b860a4a7bc/BLOOD_BLD-2022-016040-fx1.jpg

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