基质细胞与肿瘤细胞的相互作用通过CD40/RANK-KDM6B-NF-κB轴促进GCB-DLBCL细胞的存活。

IF 12.1 1区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Molecular Therapy Pub Date : 2025-07-02 Epub Date: 2025-03-20 DOI:10.1016/j.ymthe.2025.03.025
Dandan Liu, Haohao Zhang, Yiwang Zhang, Liping Xiao, Jingyao Wang, Shiyan Liao, Hongrui Chen, Huilian Wu, Yiming Hu, Yuhang Jiang, Qi Wang, Cuifeng Li, Pengfei Chen, Yu Zhan, Lingling Li, Ningxia Xie, Deji Ye, Donglin Sun, Yingyong Hou, Yufang Shi, Yongzhong Liu, Jiang Zhu, Wei Li, Chunkui Shao, Xiaoren Zhang
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引用次数: 0

摘要

在生发中心b细胞样弥漫性大b细胞淋巴瘤(GCB-DLBCL)中,基质细胞作为肿瘤微环境的主要组成部分可能是导致治疗耐药和复发的原因。为了研究肿瘤细胞与基质细胞之间的相互作用,我们建立了GCB-DLBCL患者源性异种移植(PDX)模型,分离原代肿瘤细胞并与基质细胞共培养。此外,我们提出了组织病理学证实的GCB-DLBCL病例,并分析了在线数据库以探索其潜在机制。我们发现在基质细胞上表达的CD40配体(CD40L)激活了GCB-DLBCL肿瘤细胞的CD40通路,保护肿瘤细胞免于凋亡,并上调RANK配体(RANKL)。而在肿瘤细胞上表达的RANKL增强了基质细胞中CD40L和BAFF的表达,进而通过激活NF-κB信号通路促进肿瘤细胞存活。值得注意的是,CD40通路的激活上调了赖氨酸特异性去甲基化酶KDM6B,而KDM6B进一步增强了NF-κB信号的转录活性,这在B细胞中尚未报道。在这里,我们提供了令人信服的证据,证明基质细胞和肿瘤细胞之间的相互作用是GCB-DLBCL中真正的抗凋亡因子。这种相互作用主要涉及CD40/RANK-KDM6B-NF-κB轴,这是GCB-DLBCL的一个有希望的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interaction between stromal cells and tumor cells promotes GCB-DLBCL cell survival via the CD40/RANK-KDM6B-NF-κB axis.

The stromal cells as the main component of the tumor microenvironment in germinal center B cell-like diffuse large B cell lymphoma (GCB-DLBCL) probably is accountable for therapy resistance and relapse. To investigate the interaction between tumor cells and stromal cells, we established GCB-DLBCL patient-derived xenograft models to isolate primary tumor cells and coculture them with stromal cells. Additionally, we presented GCB-DLBCL cases with histopathologic confirmation and analyzed the online databases to explore the underlying mechanisms. We demonstrated that CD40 ligand (CD40L) expressed on stromal cells activated the CD40 pathway in GCB-DLBCL tumor cells, protecting tumor cells from apoptosis and up-regulating RANK ligand (RANKL). The RANKL expressed on tumor cells enhanced the expression of CD40L and BAFF in stromal cells, which in turn promoted tumor cells survival through activating NF-κB signaling. Significantly, the activation of CD40 pathway up-regulated KDM6B, a lysine-specific demethylase, and KDM6B further enhanced the transcription activity of NF-κB signaling, which has not been reported in B cells. Here, we provided compelling evidence that the interaction between stromal cells and tumor cells functions as a bona fide anti-apoptotic factor in GCB-DLBCL. This interaction mainly involves the CD40/RANK-KDM6B-NF-κB axis, which represents a promising therapeutic target for GCB-DLBCL.

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来源期刊
Molecular Therapy
Molecular Therapy 医学-生物工程与应用微生物
CiteScore
19.20
自引率
3.20%
发文量
357
审稿时长
3 months
期刊介绍: Molecular Therapy is the leading journal for research in gene transfer, vector development, stem cell manipulation, and therapeutic interventions. It covers a broad spectrum of topics including genetic and acquired disease correction, vaccine development, pre-clinical validation, safety/efficacy studies, and clinical trials. With a focus on advancing genetics, medicine, and biotechnology, Molecular Therapy publishes peer-reviewed research, reviews, and commentaries to showcase the latest advancements in the field. With an impressive impact factor of 12.4 in 2022, it continues to attract top-tier contributions.
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