乳腺癌中肿瘤相关巨噬细胞的靶向成像

Yanni Xu, Yunting Zeng, Xiaoyun Xiao, Hejun Liu, Boyang Zhou, B. Luo, Phei Er Saw, Q. Jiang
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引用次数: 1

摘要

乳腺癌是一种高度异质性的疾病,缺乏预后标志物。肿瘤微环境中的肿瘤相关巨噬细胞(tam)与乳腺癌的远处转移和较差的预后有关。因此,监测tam可以指导预后评估。本研究探索了一种基于两步点击化学程序的成像模式,用于检测乳腺癌中的tam。制备了甘露糖靶向脂质体(man - lipop - aag)和包封Ac4GalNAz的非靶向脂质体(lipop - aag),并对其进行了综合表征。制备的man - lipop - aag和lipop - aag的粒径分别为126±0.22 nm和93±0.23 nm。体外研究表明,RAW264.7细胞对man -脂质aag的摄取高于脂质aag。此外,流式细胞术和共聚焦显微镜证实,man - lipop - aag组RAW264.7细胞膜上存在明亮、均匀的荧光标记。此外,体内分析表明,与脂肪- aag相比,man - lipop - aag在4T1异种移植模型中积累更多,并且被甘露糖过表达的tam吸收更多。本研究描述了一种通过代谢糖工程进行特异性和非侵入性tam靶向成像的有前途的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeted Imaging of Tumor Associated Macrophages in Breast Cancer
Breast cancer is a highly heterogeneous disease lacking prognostic markers. Tumor-associated macrophages (TAMs) in the tumor microenvironment are associated with distant metastasis as well as poorer outcomes in breast cancer. Therefore, monitoring TAMs may guide prognostic assessment. This study explores an imaging modality based on a two-step click chemistry procedure for detecting TAMs in breast cancer. Mannose-targeted liposomes (MAN-lipo-AAG) and non-targeted liposomes (lipo-AAG) encapsulating Ac4GalNAz were prepared and comprehensively characterized. The sizes of the prepared MAN-lipo-AAG and lipo-AAG were 126 ± 0.22 and 93 ± 0.23 nm, respectively. In vitro studies demonstrated higher uptake of MAN-lipo-AAG than lipo-AAG by RAW264.7 cells. Moreover, flow cytometry and confocal microscopy confirmed that bright, homogeneous fluorescence labeling was present on RAW264.7 cell membranes in the MAN-lipo-AAG group. Furthermore, in vivo analysis indicated that MAN-lipo-AAG, compared with lipo-AAG, had higher accumulation in a 4T1 xenograft model and higher uptake by mannose-overexpressing TAMs. This study describes a promising approach for specific and non-invasive TAM-targeted imaging via metabolic glycoengineering.
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CiteScore
5.40
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