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IL28-B reprograms tumor-associated macrophages (TAM) to promote anti-tumor effects in colon cancer
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  • Dalei Cheng,
  • Haiyan Wang,
  • Hongyan Cheng,
  • Hui Zhang,
  • Guanjun Dong,
  • Fenglian Yan,
  • Zhaochen Ning,
  • Li Wei,
  • Xin Zhang,
  • Qun Ma,
  • Junfeng Zhang,
  • Huabao Xiong
Dalei Cheng
Shandong University Cheeloo College of Medicine
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Haiyan Wang
Shandong University Cheeloo College of Medicine
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Hongyan Cheng
Shandong University Cheeloo College of Medicine
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Hui Zhang
Jining Medical University
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Guanjun Dong
Jining Medical University
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Fenglian Yan
Jining Medical University
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Zhaochen Ning
Jining Medical University
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Li Wei
Affiliated Hospital of Jining Medical University
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Xin Zhang
Weifang Medical University School of Medical Laboratory
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Qun Ma
Jining Medical University
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Junfeng Zhang
Jining Medical University
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Huabao Xiong
Jining Medical University

Corresponding Author:[email protected]

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Abstract

The type III interferon family (IFN-III), including IFN-λ3 (IL-28B), has antiviral, anti-tumor, and immunomodulatory activities. Although IL-28B anti-tumor effect has been extensively explored, its underlying anti-tumor mechanism remains unclear. Here, we explored IL-28B effects on colon cancer. We found that IL-28B significantly inhibited colon cancer growth in a murine MC38 tumor cell engraftment model. Interestingly, IL-28B did not directly promote apoptosis or inhibit MC38 tumor cell proliferation in vitro. IL-28B treatment exerted indirect anti-tumor activity by downregulating M2 macrophages in the tumor microenvironment. Furthermore, IL-28B inhibited M2 macrophage polarization in vitro. It also halted M2 macrophage differentiation predominantly via inhibition of the STAT3 and JNK signaling pathways. Our findings revealed that IL-28B inhibited M2 macrophages in the tumor microenvironment to delay colon cancer progression. Our study provides new evidence of IL-28B anti-tumor and immunomodulatory activities.