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Updated: May 10, 2026

Induction of Intestinal Inflammation by Adoptive Transfer of CBir1 TCR Transgenic CD4+ T Cells to Immunodeficient Mice
Published on: December 16, 2021
TREM-1 inhibition attenuates inflammation and tumor within the colon
Jiangang Zhou1, Feng Chai, Guang Lu
1Department of Oncology, Zhejiang Xiaoshan Hospital, Hangzhou, China.
Abstract:
The role of myeloid cell receptor TREM-1 as an amplifier of inflammation has been widely accepted and more interestingly, TREM-1 has been implicated in tumorigenesis. However, it is not clear whether TREM-1 links colon inflammation and tumor in vivo. This study aimed to investigate whether inhibition of proinflammatory TREM-1 would prevent aberrant inflammation and tumor development within the colon. In the present study, the mouse model of DSS-induced colitis and colitis-associated tumorigenesis was used. In vivo, the treatment with the TREM-1 antagonist LP17 or control peptide was initiated at the beginning of or after induction of experimental colitis or colitis-associated tumorigenesis. As a result, TREM-1 inhibition by LP17 treatment ameliorated the development of inflammation and tumor within the colon through exerting anti-inflammatory effects. In addition, LP17 decreased intestinal epithelial proliferation in DSS-induced colitis. Taken together, TREM-1 plays critical roles in colon inflammation and tumor and targeting TREM-1 may represent a novel therapeutic strategy for colon inflammation and associated cancer.
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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