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Updated: Feb 19, 2026

Author Spotlight: Unveiling Transmembrane Protein Family-Related Markers in Gastric Cancer and Implications for Targeted Therapies
Published on: September 15, 2023
High TREM2 expression correlates with poor prognosis in gastric cancer
Xiaojing Zhang1, Wei Wang2, Peng Li3
1Department of Clinical Bio-bank, Nantong University Affiliated Hospital, Nantong, Jiangsu 226001, China; Department of Pathology, Medical School of Nantong University, Nantong, Jiangsu 226001, China.
Abstract:
Triggering receptor expressed on myeloid cells 2 (TREM2) is a member of the immunoglobulin superfamily and associates with TYRO protein tyrosine kinase-binding protein at the cell membrane to form a receptor signaling complex. Gastric cancer (GC) is one of the most common human cancers in the world. We found that TREM2 expressions in GC and adjacent tissues were significantly different. The goal of this study was to measure TREM2 protein and mRNA expression levels in GC tissues and evaluate their value as potential prognostic markers. We analyzed TREM2 mRNA and protein expression by quantitative real-time polymerase chain reaction and immunohistochemistry, respectively, in 317 samples of GC tissue, matched normal tissue, or benign gastric lesions. The associations between TREM2 level and various clinicopathologic characteristics were assessed, and the correlation between TREM2 expression and prognosis of GC patients was analyzed using Oncomine and Kaplan-Meier Plotter online resources. TREM2 mRNA and protein expression levels were both significantly higher in GC compared with normal gastric tissues (P<.0001 and P<.001, respectively). Among the clinicopathological characteristics evaluated, differentiation (P<.05), N stage (P<.001), and TNM stage (P<.001) were all significantly associated with high TREM2 expression. TREM2 levels were inversely correlated with patient prognosis. Our data suggest that TREM2 expression could be an effective prognostic biomarker for GC.
Insights
Triggering receptor expressed on myeloid cells 2 (TREM2) is elevated in gastric cancer tissues. Higher TREM2 expression correlates with advanced disease stages and poorer patient prognosis, suggesting its potential as a biomarker.
Area of Science:
- Immunology
- Oncology
Background:
- Triggering receptor expressed on myeloid cells 2 (TREM2) is an immunoglobulin superfamily member.
- TREM2 forms a signaling complex with TYRO protein tyrosine kinase-binding protein at the cell membrane.
- Gastric cancer (GC) is a prevalent and significant global health concern.
Purpose of the Study:
- To quantify TREM2 protein and mRNA expression in GC tissues.
- To assess the prognostic value of TREM2 in GC patients.
Main Methods:
- Analysis of 317 GC tissue samples, adjacent normal tissues, and benign gastric lesions.
- Quantitative real-time polymerase chain reaction (qRT-PCR) for mRNA expression.
- Immunohistochemistry (IHC) for protein expression.
- Utilized Oncomine and Kaplan-Meier Plotter for data analysis.
Main Results:
- TREM2 mRNA and protein levels were significantly higher in GC tissues compared to normal gastric tissues (P<.0001 and P<.001, respectively).
- High TREM2 expression was significantly associated with poor differentiation (P<.05), advanced N stage (P<.001), and TNM stage (P<.001).
- TREM2 expression levels showed an inverse correlation with patient prognosis.
Conclusions:
- TREM2 is upregulated in gastric cancer.
- TREM2 expression serves as a potential prognostic biomarker for gastric cancer.
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