体内
Wnt信号通路
下调和上调
体外
癌症研究
药品
淋巴瘤
调解人
生物
免疫学
调节器
医学
疾病
持久性(不连续性)
转录调控
弥漫性大B细胞淋巴瘤
临床试验
耐火材料(行星科学)
离体
信号转导
机制(生物学)
核糖核酸
药理学
细胞生长
转录组
细胞培养
受体
临床研究阶段
药物开发
作者
X Li,Mengke Liu,Qing Shi,Zhi-Shan Du,Di Fu,Ying Fang,Liang-Juan Zhao,Yuting Dai,Mu‐Chen Zhang,Fan Zhang,Yan Zhao,Hong-Mei Yi,Y Yiannian He,Shu Cheng,Peng-Peng Xu,Li Wang,Jiahao Chen,Weili Zhao
出处
期刊:Blood
[Elsevier BV]
日期:2026-02-27
标识
DOI:10.1182/blood.2025031156
摘要
Relapsed or refractory (R/R) disease occurs in up to 40% of diffuse large B-cell lymphoma (DLBCL) patients following first-line immunochemotherapy. However the molecular mechanisms underlying drug persistence remain incompletely defined. Here, we performed single-cell RNA and B-cell receptor sequencing on paired diagnostic and R/R samples from eight patients who were either treatment-refractory or relapsed after remission, and validated our findings in three independent patient cohorts. We found that drug-persistent cells exhibited a transcriptional profile indicative of a less-differentiated state and adopted a memory B cell-like program with enhanced stem-like properties, which correlated with unfavorable clinical outcomes across multiple DLBCL cohorts. Functionally, drug-persistent cells showed significantly increased in vitro clonogenicity and in vivo tumor-initiating capacity. Mechanistically, the WNT signaling regulator CSNK1E was upregulated in these stem-like drug-persistent cells, in part through the activation of the APRIL-TNFRSF13B axis. Notably, CSNK1E inhibition impaired the growth and tumor-initiating capacity of drug-persistent cells and potentiated the efficacy of R-CHOP-based treatment both in vitro and in vivo. Together, our study reveals the stem-like transcriptional and functional properties of drug-persistent cells, and identifies CSNK1E as a critical mediator and therapeutic vulnerability to improve the efficacy of standard immunochemotherapy in DLBCL.
科研通智能强力驱动
Strongly Powered by AbleSci AI