Biofilm Potentiates Cancer‐Promoting Effects of Tumor‐Associated Macrophages in a 3D Multi‐Faceted Tumor Model

Author:

Deng Yanlin1ORCID,Fu Yatian12,Chua Song Lin3456,Khoo Bee Luan127ORCID

Affiliation:

1. Department of Biomedical Engineering City University of Hong Kong Kowloon 999077 Hong Kong

2. Hong Kong Center for Cerebro‐Cardiovascular Health Engineering (COCHE) Kowloon 999077 Hong Kong

3. Department of Applied Biology and Chemical Technology The Hong Kong Polytechnic University Hong Kong SAR Kowloon 999077 China

4. State Key Laboratory of Chemical Biology and Drug Discovery The Hong Kong Polytechnic University Hong Kong SAR Kowloon 999077 China

5. Shenzhen Key Laboratory of Food Biological Safety Control Kowloon 999077 Hong Kong

6. Research Centre for Deep Space Explorations (RCDSE) The Hong Kong Polytechnic University Hong Kong SAR Kowloon 999077 China

7. Department of Precision Diagnostic and Therapeutic Technology City University of Hong Kong Shenzhen‐Futian Research Institute Shenzhen 518057 China

Abstract

AbstractComponents 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 (TAMPIEB) 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.

Funder

City University of Hong Kong

Environment and Conservation Fund

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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