TREM-1 inhibition attenuates inflammation and tumor within the colon

Jiangang Zhou1, Feng Chai, Guang Lu

  • 1Department of Oncology, Zhejiang Xiaoshan Hospital, Hangzhou, China.

Insights

Targeting TREM-1 (triggering receptor expressed on myeloid cells-1) can reduce colon inflammation and tumor growth. Inhibition of TREM-1 ameliorated colitis and associated tumorigenesis in a mouse model, suggesting a novel therapeutic strategy.

Area of Science:

  • Immunology
  • Gastroenterology
  • Oncology

Background:

  • Triggering receptor expressed on myeloid cells-1 (TREM-1) amplifies inflammation and is implicated in tumorigenesis.
  • The specific link between TREM-1, colon inflammation, and tumor development in vivo remains unclear.

Purpose of the Study:

  • To investigate if inhibiting the pro-inflammatory TREM-1 receptor can prevent aberrant inflammation and tumor development in the colon.
  • To explore TREM-1's role in linking colon inflammation and cancer.

Main Methods:

  • Utilized a mouse model of dextran sulfate sodium (DSS)-induced colitis and colitis-associated tumorigenesis.
  • Administered the TREM-1 antagonist LP17 or a control peptide during or after the induction of experimental colitis or tumorigenesis.
  • Assessed the effects of TREM-1 inhibition on inflammation, tumor development, and intestinal epithelial proliferation.

Main Results:

  • TREM-1 inhibition using LP17 treatment significantly ameliorated colon inflammation and tumor development.
  • LP17 demonstrated anti-inflammatory effects, reducing the severity of colitis.
  • TREM-1 inhibition also decreased intestinal epithelial proliferation in the DSS-induced colitis model.

Conclusions:

  • TREM-1 plays a critical role in both colon inflammation and tumor development.
  • Targeting TREM-1 presents a potential novel therapeutic strategy for managing colon inflammation and associated cancers.
  • Inhibition of TREM-1 offers a promising approach for treating inflammatory bowel disease and colorectal cancer.

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