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Updated: Jun 14, 2025

Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
Bidirectional interaction between epithelial-mesenchymal transition and PD-1/PD-L1 expression in tongue
Hannah Gil de Farias Morais1, Helder Domiciano Dantas Martins2, Alexandre Rolim da Paz3
1Department of Oral Pathology, Federal University of Rio Grande do Norte, Natal, Brazil; Federal University of Rio Grande do Norte. Multicampi School of Medical Sciences, Caicó, Brazil.
Epithelial-mesenchymal transition (EMT) is prevalent in oral tongue squamous cell carcinoma (OTSCC) and correlates with immune checkpoint proteins PD-1 and PD-L1. This suggests EMT may drive an immunosuppressive tumor microenvironment in OTSCC.
Area of Science:
- Oncology
- Immunology
- Cell Biology
Background:
- Oral tongue squamous cell carcinoma (OTSCC) is a significant head and neck cancer.
- Epithelial-mesenchymal transition (EMT) is a cellular process implicated in cancer progression and metastasis.
- Immune checkpoint proteins, such as PD-1 and PD-L1, are crucial regulators of the anti-tumor immune response.
Purpose of the Study:
- To investigate the association between EMT and the expression of immune checkpoint proteins PD-1 and PD-L1 in OTSCC.
- To explore the relationship between EMT status, PD-1/PD-L1 expression, and clinicopathological variables in OTSCC.
- To determine the prognostic implications of EMT and PD-1/PD-L1 expression on patient survival in OTSCC.
Main Methods:
- Immunohistochemistry was employed to assess E-cadherin and N-cadherin expression for EMT status determination.
- Semiquantitative analysis of PD-1 and PD-L1 immunoexpression was performed on 61 OTSCC tissue samples.
- Statistical analyses were conducted to correlate EMT status and PD-1/PD-L1 expression with clinicopathological features and survival rates (OS and DFS).
Main Results:
- A high prevalence of positive EMT status (75.4%) was observed in OTSCC, significantly associated with higher histological grade (p=0.003).
- Increased PD-L1 expression was significantly linked to larger tumor size (p=0.048).
- Positive EMT status correlated with higher immunoexpression of both PD-1 (p=0.003) and PD-L1 (p=0.001), with a moderate positive correlation between PD-1 and PD-L1 expression (r=0.571, p<0.001).
Conclusions:
- EMT is a frequent event in OTSCC and is associated with increased expression of PD-1 and PD-L1.
- The findings suggest that EMT may contribute to the development of an immunosuppressive tumor microenvironment in OTSCC.
- Targeting EMT or immune checkpoints could represent potential therapeutic strategies for OTSCC.
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