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A mineralization strategy based on T-cell membrane coated CaCO3 nanoparticles against breast cancer and metastasis
Materials Chemistry Frontiers ( IF 6.0 ) Pub Date : 2021-6-3 , DOI: 10.1039/d1qm00464f Yanhua Li 1, 2, 3, 4, 5 , Xia Zhang 1, 2, 3, 4, 5 , Xiaohan Liu 1, 2, 3, 4, 5 , Wei Pan 1, 2, 3, 4, 5 , Na Li 1, 2, 3, 4, 5 , Bo Tang 1, 2, 3, 4, 5
Materials Chemistry Frontiers ( IF 6.0 ) Pub Date : 2021-6-3 , DOI: 10.1039/d1qm00464f Yanhua Li 1, 2, 3, 4, 5 , Xia Zhang 1, 2, 3, 4, 5 , Xiaohan Liu 1, 2, 3, 4, 5 , Wei Pan 1, 2, 3, 4, 5 , Na Li 1, 2, 3, 4, 5 , Bo Tang 1, 2, 3, 4, 5
Affiliation
Chemotherapy has always been ineffective against cancer metastasis due to the limited diffusion ability of passive agents into the internal tumor. Herein, we designed a mineralization strategy based on multifunctional calcium carbonate nanoparticles (CaFAM) for treating breast cancer and inhibiting metastasis. CaFAM consisted of CaCO3 nanoparticles loaded with folic acid molecules (FA) and coated with the T-cell membrane. In the acidic tumor microenvironment, CaCO3 disintegrates to release calcium ions (Ca2+) and FA. The released FA molecules conjugate to cancer cells by folate receptors, and then mediate Ca2+ to mineralize, which results in the suppression of migration, invasion and proliferation of cancer cells. Particularly, the T-cell membrane gives materials the ability to target tumors and avoids the immune clearance of the body. The tumor treatment results demonstrate that CaFAM provides a potential method for tumor treatment.
中文翻译:
基于 T 细胞膜包覆 CaCO3 纳米颗粒的矿化策略对乳腺癌和转移
由于被动药物进入内部肿瘤的扩散能力有限,化疗一直对癌症转移无效。在此,我们设计了一种基于多功能碳酸钙纳米粒子(CaFAM)的矿化策略,用于治疗乳腺癌和抑制转移。CaFAM 由装载有叶酸分子 (FA) 并涂有 T 细胞膜的 CaCO 3纳米颗粒组成。在酸性肿瘤微环境中,CaCO 3分解释放钙离子(Ca 2+)和FA。释放的 FA 分子通过叶酸受体与癌细胞结合,然后介导 Ca 2+矿化,从而抑制癌细胞的迁移、侵袭和增殖。特别是,T 细胞膜使材料能够靶向肿瘤并避免身体的免疫清除。肿瘤治疗结果表明,CaFAM 为肿瘤治疗提供了一种潜在的方法。
更新日期:2021-06-22
中文翻译:
基于 T 细胞膜包覆 CaCO3 纳米颗粒的矿化策略对乳腺癌和转移
由于被动药物进入内部肿瘤的扩散能力有限,化疗一直对癌症转移无效。在此,我们设计了一种基于多功能碳酸钙纳米粒子(CaFAM)的矿化策略,用于治疗乳腺癌和抑制转移。CaFAM 由装载有叶酸分子 (FA) 并涂有 T 细胞膜的 CaCO 3纳米颗粒组成。在酸性肿瘤微环境中,CaCO 3分解释放钙离子(Ca 2+)和FA。释放的 FA 分子通过叶酸受体与癌细胞结合,然后介导 Ca 2+矿化,从而抑制癌细胞的迁移、侵袭和增殖。特别是,T 细胞膜使材料能够靶向肿瘤并避免身体的免疫清除。肿瘤治疗结果表明,CaFAM 为肿瘤治疗提供了一种潜在的方法。