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TRIM Expression in HNSCC: Exploring the Link Between Ubiquitination, Immune Infiltration, and Signaling Pathways
Kun Wang1, Wei Zhu2, Wei Huang3
1Department of Clinical Laboratory, Xiangya Hospital, Central South University, Changsha, Hunan Province, People's Republic of China.
Objective:
Ubiquitination is an important post-translational modification. However, the significance of the TRIM family of E3 ubiquitin ligases in head and neck squamous cell carcinoma (HNSCC) has not been determined. In this study, the roles of TRIM E3 ubiquitin ligases in lymphovascular invasion in head and neck squamous cell carcinoma (HNSCC) were evaluated.
Materials And Methods:
TRIM expression and related parameters were obtained from UbiBrowser2.0, UALCAN, TIMER, TISIDB, LinkedOmics, STRING, and GeneMANIA databases. Immunohistochemistry was used to confirm their expression.
Results:
TRIM2, TRIM11, TRIM28, and TRIM56 were upregulated in HNSCC with lymphovascular invasion. TRIM expression was strongly associated with immune infiltration, including key treatment targets, like PD-1 and CTL4. Co-expressed genes and possible ubiquitination substrates included tumor-related factors. The TRIMs had predicted roles in ubiquitination-related pathways and vital signaling pathways, eg, MAPK, PI3K-Akt, and JAK-STAT signaling pathways.
Conclusion:
Ubiquitination mediated by four TRIMs might be involved in the regulation of tumor immunity, laying the foundation for future studies of the roles of the TRIM family on the prediction and personalized medicine in HNSCC. The four TRIMs might exert oncogenic effects by promoting lymphovascular invasion in HNSCC.
Insights
Four TRIM E3 ubiquitin ligases (TRIM2, TRIM11, TRIM28, TRIM56) are upregulated in head and neck squamous cell carcinoma (HNSCC) and promote lymphovascular invasion. These TRIMs also correlate with immune infiltration, suggesting roles in tumor immunity and personalized HNSCC medicine.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Ubiquitination is a critical post-translational modification.
- The role of TRIM E3 ubiquitin ligases in head and neck squamous cell carcinoma (HNSCC) remains largely undetermined.
- Lymphovascular invasion is a key factor in HNSCC progression and metastasis.
Purpose of the Study:
- To investigate the significance of TRIM E3 ubiquitin ligases in lymphovascular invasion within HNSCC.
- To explore the association between TRIM expression, immune infiltration, and signaling pathways in HNSCC.
Main Methods:
- Utilized multiple bioinformatics databases (UbiBrowser 2.0, UALCAN, TIMER, TISIDB, LinkedOmics, STRING, GeneMANIA) to analyze TRIM expression and related parameters.
- Confirmed TRIM expression in HNSCC using immunohistochemistry.
- Analyzed co-expressed genes, ubiquitination substrates, and signaling pathway involvement.
Main Results:
- TRIM2, TRIM11, TRIM28, and TRIM56 were found to be upregulated in HNSCC exhibiting lymphovascular invasion.
- TRIM expression showed a strong correlation with immune cell infiltration, including associations with PD-1 and CTLA-4.
- Predicted roles for TRIMs in ubiquitination, tumor-related pathways, and key signaling cascades (MAPK, PI3K-Akt, JAK-STAT).
Conclusions:
- Ubiquitination mediated by these four TRIMs may play a role in regulating tumor immunity in HNSCC.
- The identified TRIMs could serve as potential biomarkers for predicting lymphovascular invasion and guiding personalized medicine approaches in HNSCC.
- These TRIMs may exert oncogenic effects by promoting lymphovascular invasion in HNSCC.
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