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CMTM3 as a Potential New Immune Checkpoint Regulator.
Qian Shen1, Zhirong Cong1, Ying Zhou1
1Department of Hematologic Lymphoma, Affiliated Cancer Hospital of Nantong University, Nantong, China.
Journal of Oncology
|October 17, 2022
Summary
CKLF-like MARVEL transmembrane domain containing 3 (CMTM3) is linked to poor cancer survival and influences the tumor microenvironment. This suggests CMTM3 could be a biomarker and therapeutic target for cancer immunotherapy.
Area of Science:
- Oncology
- Immunology
- Genomics
Background:
- The tumor microenvironment significantly impacts cancer progression and treatment response.
- Understanding novel molecular players in cancer immunity is crucial for developing effective therapies.
Purpose of the Study:
- To investigate the role of CKLF-like MARVEL transmembrane domain containing 3 (CMTM3) in the tumor microenvironment.
- To explore CMTM3's potential as a biomarker and therapeutic target in cancer immunotherapy.
- To elucidate the mechanisms underlying CMTM3's influence on anti-cancer immunity.
Main Methods:
- Utilized RNAseq data from GTEx and TCGA databases for CMTM3 expression and prognostic analysis.
- Performed enrichment analysis using the R package "clusterProfiler."
- Assessed immune cell infiltration using ImmuCellAI and TIMER2 databases, correlating with CMTM3 expression and immune-related genes.
Main Results:
- CMTM3 expression varied across tumor types and was associated with poor survival outcomes.
- CMTM3 expression correlated with key tumor microenvironment components, including cancer-associated fibroblasts and immune cells.
- Significant associations were found between CMTM3 and immune activation/suppression genes, immune checkpoints, and chemokine pathways.
Conclusions:
- CMTM3 shows potential as a predictive biomarker for cancer prognosis.
- CMTM3 may modulate the immune microenvironment, offering a target for novel cancer immunotherapy strategies.
- Further research into CMTM3's interaction with immune checkpoints could lead to new therapeutic developments.

