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泽布替尼可延缓活检样本来源的原发性中枢神经系统淋巴瘤模型中塞利尼索耐药性的演变。

Zanubrutinib delays selinexor resistance evolution in biopsy sample-derived primary central nervous system lymphoma models.

作者信息

Zheng Xiaohong, Wang Can, Chen Feng, Li Shenglan, Zhang Hua, Dong Gehong, Yang Shoubo, Kang Xun, Kang Zhuang, Han Chunlei, Yin Shuo, Li Wenbin

机构信息

Department of Neuro-Oncology, Cancer Center, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

出版信息

iScience. 2024 Apr 23;27(5):109799. doi: 10.1016/j.isci.2024.109799. eCollection 2024 May 17.

Abstract

Primary central nervous system lymphoma (PCNSL) is a rare and aggressive lymphoma of the brain with poor prognosis. The scarcity of cell lines established using PCNSL makes it difficult to conduct preclinical studies on new drugs. We aimed to explore the effect of selinexor combined with zanubrutinib in PCNSL using established PCNSL cells and an orthotopic PCNSL model. Primary PCNSL cells were successfully cultured. Selinexor inhibited proliferation, induced G1 phase arrest, and promoted apoptosis, however, induced drug resistance in PCNSL. Selinexor combined with zanubrutinib had a synergistic effect on PCNSL and prevented the onset of selinexor resistance in PCNSL by inhibiting AKT signaling. Moreover, selinexor combined with zanubrutinib notably slowed tumor growth and prolonged survival compared to that of the control. Overall, the addition of zanubrutinib to selinexor monotreatment had a synergistic effect and prolonged survival .

摘要

原发性中枢神经系统淋巴瘤(PCNSL)是一种罕见的侵袭性脑淋巴瘤,预后较差。利用PCNSL建立的细胞系稀缺,这使得对新药进行临床前研究变得困难。我们旨在使用已建立的PCNSL细胞和原位PCNSL模型,探索塞利尼索联合泽布替尼对PCNSL的影响。原发性PCNSL细胞成功培养。塞利尼索抑制增殖,诱导G1期阻滞,并促进凋亡,然而,其会诱导PCNSL产生耐药性。塞利尼索联合泽布替尼对PCNSL具有协同作用,并通过抑制AKT信号传导防止PCNSL中塞利尼索耐药的发生。此外,与对照组相比,塞利尼索联合泽布替尼显著减缓了肿瘤生长并延长了生存期。总体而言,在塞利尼索单药治疗中加入泽布替尼具有协同作用并延长了生存期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4db8/11079464/4dd80152cafe/fx1.jpg

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