肿瘤微环境
癌症研究
肿瘤进展
生物膜
癌症
免疫疗法
炎症
免疫系统
巨噬细胞极化
转移
癌症免疫疗法
癌细胞
生物
巨噬细胞
免疫学
肿瘤细胞
体外
细菌
生物化学
遗传学
作者
Yanlin Deng,Yatian Fu,Song Lin Chua,Bee Luan Khoo
出处
期刊:Small
[Wiley]
日期:2023-02-07
卷期号:19 (19)
被引量:11
标识
DOI:10.1002/smll.202205904
摘要
Abstract Components of the tumor microenvironment (TME), such as tumor‐associated macrophages (TAMs), influence tumor progression. The specific polarization and phenotypic transition of TAMs in the tumor microenvironment lead to two‐pronged impacts that can promote or hinder cancer development and treatment. Here, a novel microfluidic multi‐faceted bladder tumor model (TAM PIEB ) is developed incorporating TAMs and cancer cells to evaluate the impact of bacterial distribution on immunomodulation within the tumor microenvironment in vivo. It is demonstrated for the first time that biofilm‐induced inflammatory conditions within tumors promote the transition of macrophages from a pro‐inflammatory M1‐like to an anti‐inflammatory/pro‐tumor M2‐like state. Consequently, multiple roles and mechanisms by which biofilms promote cancer by inducing pro‐tumor phenotypic switch of TAMs are identified, including cancer hallmarks such as reducing susceptibility to apoptosis, enhancing cell viability, and promoting epithelial‐mesenchymal transition and metastasis. Furthermore, biofilms formed by extratumoral bacteria can shield tumors from immune attack by TAMs, which can be visualized through various imaging assays in situ. The study sheds light on the underlying mechanism of biofilm‐mediated inflammation on tumor progression and provides new insights into combined anti‐biofilm therapy and immunotherapy strategies in clinical trials.
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