Division of Hematology, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Department of Medicine, University of Miami Miller School of Medicine, Miami, FL 33136, USA.
Cells. 2024 Nov 6;13(22):1835. doi: 10.3390/cells13221835.
Lymphoma growth, progression, and dissemination require tumor cell interaction with supporting vessels and are facilitated through tumor-promoted angiogenesis, lymphangiogenesis, and/or lymphoma vessel co-option. Vessel co-option has been shown to be responsible for tumor initiation, metastasis, and resistance to anti-angiogenic treatment but is largely uncharacterized in the setting of lymphoma. We developed an in vitro model to study lymphoma-vessel interactions and found that mantle cell lymphoma (MCL) cells co-cultured on Matrigel with human umbilical vein (HUVEC) or human lymphatic (HLEC) endothelial cells migrate to and anneal with newly formed capillary-like (CLS) or lymphatic-like (LLS) structures, consistent with lymphoma-vessel co-option. To inhibit this interaction, we constructed an antibody fusion protein, αCD20-EndoP125A, linking mutant anti-angiogenic endostatin (EndoP125A) to an αCD20-IgG1-targeting antibody. αCD20-EndoP125A inhibited both CLS and LLS formation, as well as MCL migration and vessel co-option. Lymphoma vessel co-option requires cell migration, which is regulated by chemokine-chemokine receptor interactions. CXCL12 and its receptor, CXCR4, are highly expressed by both endothelial cells forming CLS and by MCL cells during vessel co-option. αCD20-EndoP125A suppressed expression of both CXCL12 and CXCR4, which were required to facilitate CLS assembly and vessel co-option. We also tested αCD20-EndoP125A effects in vivo using an aggressive murine B cell lymphoma model, 38c13-hCD20, which demonstrated rapid growth and dissemination to tumor-draining lymph nodes (TDLNs) and the spleen, lung, and brain. The pattern of lymphoma distribution and growth within the lung was consistent with vessel co-option. As predicted by our in vitro model, αCD20-EndoP125A treatment inhibited primary tumor growth, angiogenesis, and lymphangiogenesis, and markedly reduced the number of circulating tumor cells and lymphoma dissemination to TDLNs and the lungs, spleen, and brain. αCD20-EndoP125A inhibited lymphoma vessel co-option within the lung. Marked inhibition of MCL primary tumor growth and dissemination were also seen using an MCL xenograft model. The ability of αCD20-EndoP125A to inhibit angiogenesis, lymphangiogenesis, and lymphoma vessel co-option provides a novel therapeutic approach for inhibition of lymphoma progression and dissemination.
淋巴瘤的生长、进展和扩散需要肿瘤细胞与支持血管相互作用,并通过肿瘤促进的血管生成、淋巴管生成和/或淋巴瘤血管摄取来促进。血管摄取已被证明与肿瘤的起始、转移和对抗血管生成治疗的耐药性有关,但在淋巴瘤中尚未得到充分描述。我们开发了一种体外模型来研究淋巴瘤-血管相互作用,发现套细胞淋巴瘤(MCL)细胞与人类脐静脉(HUVEC)或人淋巴管(HLEC)内皮细胞共培养在 Matrigel 上,迁移并与新形成的毛细血管样(CLS)或淋巴管样(LLS)结构吻合,这与淋巴瘤-血管摄取一致。为了抑制这种相互作用,我们构建了一种抗体融合蛋白,αCD20-EndoP125A,将突变的抗血管生成内皮抑素(EndoP125A)与靶向αCD20-IgG1 的抗体连接起来。αCD20-EndoP125A 抑制了 CLS 和 LLS 的形成,以及 MCL 的迁移和血管摄取。淋巴瘤血管摄取需要细胞迁移,而细胞迁移受趋化因子-趋化因子受体相互作用的调节。CXCL12 及其受体 CXCR4 在形成 CLS 的内皮细胞和血管摄取过程中的 MCL 细胞中均高度表达。αCD20-EndoP125A 抑制了 CXCL12 和 CXCR4 的表达,这对于促进 CLS 组装和血管摄取是必需的。我们还使用侵袭性的小鼠 B 细胞淋巴瘤模型 38c13-hCD20 进行了体内测试,结果显示该模型肿瘤快速生长并扩散到肿瘤引流淋巴结(TDLNs)和脾脏、肺和脑。肺内淋巴瘤的分布和生长模式与血管摄取一致。正如我们的体外模型所预测的那样,αCD20-EndoP125A 治疗抑制了原发肿瘤的生长、血管生成和淋巴管生成,并显著减少了循环肿瘤细胞的数量和肿瘤向 TDLNs 以及肺、脾和脑的扩散。αCD20-EndoP125A 抑制了肺内的淋巴瘤血管摄取。在使用 MCL 异种移植模型时,也观察到对 MCL 原发肿瘤生长和扩散的明显抑制。αCD20-EndoP125A 抑制血管生成、淋巴管生成和淋巴瘤血管摄取的能力为抑制淋巴瘤进展和扩散提供了一种新的治疗方法。