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Lymph Node Stiffness Mimicking Hydrogels Regulate Human B Cell Lymphoma Growth and Cell Surface Receptor #Expression in a Molecular Subtype-Specific Manner

机译:模仿水凝胶的淋巴结刚度以分子亚型特异性方式调节人B细胞淋巴瘤的生长和细胞表面受体#的表达。

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Conclusions: To the best of our knowledge, our results are the first evidence that lymphoma survival, proliferation, drug response, and BCR signaling is influenced by lymphoid tissue stiffness in a molecular subtype dependent manner. These results emphasize the role of biomaterials based 3D tissues with tumor matched stiffness and the importance of lymphoid tissue stiffness in malignant B cell tumors. In the past, lymphoid tissue stiffness and mechanosensing has been largely ignored in mechanistic study lymphoma progression and its therapeutic evaluation of B cell lymphomas ex vivo. We anticipate that our findings will be broadly useful to study lymphoma biology and discover new class of therapeutics that target B cell tumors in physical environments.
机译:结论:就我们所知,我们的结果是淋巴瘤存活,增殖,药物反应和BCR信号以分子亚型依赖性方式受淋巴组织硬度影响的第一个证据。这些结果强调了具有与肿瘤匹配的刚度的基于生物材料的3D组织的作用,以及在恶性B细胞肿瘤中淋巴样组织刚度的重要性。过去,在机理研究淋巴瘤进展及其离体B细胞淋巴瘤的治疗评估中,淋巴样组织的僵硬和机械传感已被很大程度上忽略。我们希望我们的发现对研究淋巴瘤生物学和发现针对物理环境中B细胞肿瘤的新型疗法具有广泛的帮助。

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