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通过调节肿瘤内微生物群实现晚期三阴性乳腺癌治疗的纳米策略

A Nano-Strategy for Advanced Triple-Negative Breast Cancer Therapy by Regulating Intratumoral Microbiota.

作者信息

Gao Jifan, Tang Lu, Fu Cong, Cao Yuqi, Liu Hening, Yin Yue, Li Zixuan, Zhu Yuanbo, Shu Weijie, Zhang Yi, Ru Xinrong, Wang Wei

机构信息

State Key Laboratory of Natural Medicines, Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, Nanjing 211198, P. R. China.

NMPA Key Laboratory for Research and Evaluation of Cosmetics, China Pharmaceutical University, Nanjing 211198, P. R. China.

出版信息

Nano Lett. 2025 Apr 16;25(15):6134-6144. doi: 10.1021/acs.nanolett.5c00298. Epub 2025 Apr 3.

Abstract

Intratumoral microbiota have been identified as a component of the tumor microenvironment that regulates the metastatic behavior of tumors. They serve not only as indicators of tumor pathology but also as potential drug targets in cancer therapy. Herein, a multifunctional nanoplatform (DD@FEL) is prepared by combining antibiotic doxycycline (DOXY) that can combat intratumoral microbiota and the chemotherapeutic drug doxorubicin (DOX) in ergosterol-originated liposome. Specially, ergosterol is utilized as a substitute for cholesterol in liposomes to exert pharmacological activity. Mechanistically, DD@FEL leveraged DOXY to inhibit cancer metastasis based on the regulation of intratumoral microbiota, which synergizes with the chemotherapeutic effect of DOX, eventually inhibiting the progression of triple-negative breast cancer (TNBC). Verified both and , DD@FEL effectively exerts a cytotoxic effect on TNBC cells, delays the growth of primary TNBC, and attenuates the development of its lung metastasis, providing a promising therapeutic strategy to control both orthotopic and metastatic TNBC.

摘要

肿瘤内微生物群已被确定为肿瘤微环境的一个组成部分,可调节肿瘤的转移行为。它们不仅是肿瘤病理学的指标,也是癌症治疗中潜在的药物靶点。在此,通过将可对抗肿瘤内微生物群的抗生素强力霉素(DOXY)与化疗药物阿霉素(DOX)结合在麦角固醇来源的脂质体中,制备了一种多功能纳米平台(DD@FEL)。特别地,麦角固醇被用作脂质体中胆固醇的替代品以发挥药理活性。从机制上讲,DD@FEL利用DOXY基于对肿瘤内微生物群的调节来抑制癌症转移,这与DOX的化疗作用协同,最终抑制三阴性乳腺癌(TNBC)的进展。体内和体外实验均证实,DD@FEL对TNBC细胞有效发挥细胞毒性作用,延缓原发性TNBC的生长,并减轻其肺转移的发展,为控制原位和转移性TNBC提供了一种有前景的治疗策略。

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