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维奈托克在维奈托克耐药的急性髓系白血病细胞中触发亚致死性凋亡信号,并诱导对 PARP 抑制和阿扎胞苷的易感性。

Venetoclax triggers sublethal apoptotic signaling in venetoclax-resistant acute myeloid leukemia cells and induces vulnerability to PARP inhibition and azacitidine.

机构信息

Institute for Molecular Medicine Finland (FIMM), Helsinki Institute of Life Science (HiLIFE), iCAN Digital Precision Cancer Medicine Flagship, University of Helsinki, Helsinki, Finland.

Biotech Research & Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.

出版信息

Cell Death Dis. 2024 Oct 16;15(10):750. doi: 10.1038/s41419-024-07140-4.

Abstract

Venetoclax plus azacitidine treatment is clinically beneficial for elderly and unfit acute myeloid leukemia (AML) patients. However, the treatment is rarely curative, and relapse due to resistant disease eventually emerges. Since no current clinically feasible treatments are known to be effective at the state of acquired venetoclax resistance, this is becoming a major challenge in AML treatment. Studying venetoclax-resistant AML cell lines, we observed that venetoclax induced sublethal apoptotic signaling and DNA damage even though cell survival and growth were unaffected. This effect could be due to venetoclax inducing a sublethal degree of mitochondrial outer membrane permeabilization. Based on these results, we hypothesized that the sublethal apoptotic signaling induced by venetoclax could constitute a vulnerability in venetoclax-resistant AML cells. This was supported by screens with a broad collection of drugs, where we observed a synergistic effect between venetoclax and PARP inhibition in venetoclax-resistant cells. Additionally, the venetoclax-PARP inhibitor combination prevented the acquisition of venetoclax resistance in treatment naïve AML cell lines. Furthermore, the addition of azacitidine to the venetoclax-PARP inhibitor combination enhanced venetoclax induced DNA damage and exhibited exceptional sensitivity and long-term responses in the venetoclax-resistant AML cell lines and samples from AML patients that had clinically relapsed under venetoclax-azacitidine therapy. In conclusion, we mechanistically identify a new vulnerability in acquired venetoclax-resistant AML cells and identify PARP inhibition as a potential therapeutic approach to overcome acquired venetoclax resistance in AML.

摘要

维奈托克联合阿扎胞苷治疗对老年和身体不适的急性髓系白血病(AML)患者具有临床益处。然而,这种治疗很少能治愈疾病,耐药性疾病的复发最终还是会出现。由于目前尚无已知的临床可行的治疗方法对获得性维奈托克耐药有效,这在 AML 治疗中成为一个主要挑战。通过研究对维奈托克耐药的 AML 细胞系,我们观察到维奈托克诱导了亚致死性凋亡信号和 DNA 损伤,尽管细胞存活和生长不受影响。这种效应可能是由于维奈托克诱导了亚致死性程度的线粒体外膜通透性。基于这些结果,我们假设维奈托克诱导的亚致死性凋亡信号可能构成维奈托克耐药 AML 细胞的一个弱点。这一假设得到了广泛药物筛选的支持,我们观察到维奈托克耐药细胞中维奈托克和 PARP 抑制剂之间存在协同作用。此外,维奈托克-PARP 抑制剂联合用药可防止在未经治疗的 AML 细胞系中获得维奈托克耐药性。此外,在维奈托克-PARP 抑制剂联合用药中添加阿扎胞苷可增强维奈托克诱导的 DNA 损伤,并在维奈托克耐药的 AML 细胞系和接受维奈托克-阿扎胞苷治疗后临床复发的 AML 患者样本中表现出异常的敏感性和长期反应。总之,我们从机制上确定了获得性维奈托克耐药 AML 细胞中的一个新弱点,并确定 PARP 抑制作为克服 AML 中获得性维奈托克耐药的潜在治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f59/11484809/138f55fbf91e/41419_2024_7140_Fig1_HTML.jpg

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