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携带抗IL6R抗体至肿瘤微环境的脂质体纳米颗粒抑制两种分子亚型乳腺癌小鼠模型中的转移。

Liposomal Nanoparticles Carrying anti-IL6R Antibody to the Tumour Microenvironment Inhibit Metastasis in Two Molecular Subtypes of Breast Cancer Mouse Models.

作者信息

Guo Chunlei, Chen Yanan, Gao Wenjuan, Chang Antao, Ye Yujie, Shen Wenzhi, Luo Yunping, Yang Shengyong, Sun Peiqing, Xiang Rong, Li Na

机构信息

School of Medicine, Nankai University, 94 Weijin Road, Tianjin 300071, China.

Department of Immunology, Institute of Basic Medical Science, Peking Union Medical College, Beijing 100730, China.

出版信息

Theranostics. 2017 Jan 26;7(3):775-788. doi: 10.7150/thno.17237. eCollection 2017.

Abstract

Tumour microenvironment (TME) contributes significantly towards potentiating the stemness and metastasis properties of cancer cells. IL6-Stat3 is one of the important cell signaling pathways in mediating the communication between tumour and immune cells. Here, we have systematically developed a novel anti-CD44 antibody-mediated liposomal nanoparticle delivery system loaded with anti-IL6R antibody, which could specifically target the TME of CD44 breast cancer cells in different mouse models for triple negative and luminal breast cancer. This nanoparticle had an enhanced and specific tumour targeting efficacy with dramatic anti-tumour metastasis effects in syngeneic BALB/c mice bearing 4T1 cells as was in the syngeneic MMTV-PyMT mice. It inhibited IL6R-Stat3 signaling and moderated the TME, characterized by the reduced expression of genes encoding Stat3, Sox2, VEGFA, MMP-9 and CD206 in the breast tissues. Furthermore, this nanoparticle reduced the subgroups of Sox2 and CD206 cells in the lung metastatic foci, demonstrating its inhibitory effect on the lung metastatic niche for breast cancer stem cells. Taken together, the CD44 targeted liposomal nanoparticles encapsulating anti-IL6R antibody achieved a significant effect to inhibit the metastasis of breast cancer in different molecular subtypes of breast cancer mouse models. Our results shed light on the application of nanoparticle mediated cancer immune-therapy through targeting TME.

摘要

肿瘤微环境(TME)对增强癌细胞的干性和转移特性有显著作用。IL6-Stat3是介导肿瘤细胞与免疫细胞之间通讯的重要细胞信号通路之一。在此,我们系统地开发了一种新型的抗CD44抗体介导的脂质体纳米颗粒递送系统,该系统负载抗IL6R抗体,可在三阴型和管腔型乳腺癌的不同小鼠模型中特异性靶向CD44乳腺癌细胞的TME。这种纳米颗粒在携带4T1细胞的同基因BALB/c小鼠以及同基因MMTV-PyMT小鼠中具有增强的特异性肿瘤靶向功效,并具有显著的抗肿瘤转移作用。它抑制IL6R-Stat3信号传导并调节TME,其特征是乳腺组织中编码Stat3、Sox2、VEGFA、MMP-9和CD206的基因表达降低。此外,这种纳米颗粒减少了肺转移灶中Sox2和CD206细胞亚群,表明其对乳腺癌干细胞的肺转移微环境具有抑制作用。综上所述,封装抗IL6R抗体的CD44靶向脂质体纳米颗粒在不同分子亚型的乳腺癌小鼠模型中对抑制乳腺癌转移取得了显著效果。我们的研究结果为通过靶向TME的纳米颗粒介导的癌症免疫治疗的应用提供了启示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b34/5327649/34d016fd127c/thnov07p0775g001.jpg

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