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Updated: Mar 18, 2026

Intramucosal Inoculation of Squamous Cell Carcinoma Cells in Mice for Tumor Immune Profiling and Treatment Response Assessment
Published on: April 22, 2019
RAB25 expression is epigenetically downregulated in oral and oropharyngeal squamous cell carcinoma with lymph node
M J A M Clausen1,2, L J Melchers1,2, M F Mastik1
1a Departments of Pathology , University of Groningen, University Medical Center Groningen , Groningen , the Netherlands.
Abstract:
Oral and oropharyngeal squamous cell carcinoma (OOSCC) have a low survival rate, mainly due to metastasis to the regional lymph nodes. For optimal treatment of these metastases, a neck dissection is required; however, inaccurate detection methods results in under- and over-treatment. New DNA prognostic methylation biomarkers might improve lymph node metastases detection. To identify epigenetically regulated genes associated with lymph node metastases, genome-wide methylation analysis was performed on 6 OOSCC with (pN+) and 6 OOSCC without (pN0) lymph node metastases and combined with a gene expression signature predictive for pN+ status in OOSCC. Selected genes were validated using an independent OOSCC cohort by immunohistochemistry and pyrosequencing, and on data retrieved from The Cancer Genome Atlas. A two-step statistical selection of differentially methylated sequences revealed 14 genes with increased methylation status and mRNA downregulation in pN+ OOSCC. RAB25, a known tumor suppressor gene, was the highest-ranking gene in the discovery set. In the validation sets, both RAB25 mRNA (P = 0.015) and protein levels (P = 0.012) were lower in pN+ OOSCC. RAB25 mRNA levels were negatively correlated with RAB25 methylation levels (P < 0.001) but RAB25 protein expression was not. Our data revealed that promoter methylation is a mechanism resulting in downregulation of RAB25 expression in pN+ OOSCC and decreased expression is associated with lymph node metastasis. Detection of RAB25 methylation might contribute to lymph node metastasis diagnosis and serve as a potential new therapeutic target in OOSCC.
Insights
New DNA methylation biomarkers may improve the detection of lymph node metastases in oral and oropharyngeal squamous cell carcinoma (OOSCC). RAB25 gene downregulation, linked to methylation, is associated with metastasis, offering a potential diagnostic and therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- Oral and oropharyngeal squamous cell carcinoma (OOSCC) have poor survival rates, largely due to lymph node metastasis.
- Current methods for detecting lymph node metastases in OOSCC are inaccurate, leading to undertreatment or overtreatment.
- Novel prognostic methylation biomarkers are needed to improve the accuracy of metastasis detection.
Purpose of the Study:
- To identify epigenetically regulated genes associated with lymph node metastasis in OOSCC.
- To evaluate the potential of these genes as diagnostic biomarkers and therapeutic targets.
Main Methods:
- Genome-wide methylation analysis was performed on OOSCC tissues with (pN+) and without (pN0) lymph node metastases.
- Gene expression analysis was integrated to identify predictive signatures for pN+ status.
- Selected candidate genes were validated using immunohistochemistry, pyrosequencing, and The Cancer Genome Atlas (TCGA) data.
Main Results:
- Fourteen genes showed increased methylation and decreased mRNA expression in pN+ OOSCC.
- RAB25, a tumor suppressor gene, was identified as a top candidate.
- RAB25 mRNA and protein levels were significantly lower in pN+ OOSCC.
- RAB25 promoter methylation correlated negatively with mRNA levels, suggesting epigenetic silencing.
Conclusions:
- Promoter methylation leads to RAB25 downregulation in pN+ OOSCC.
- Decreased RAB25 expression is associated with lymph node metastasis.
- RAB25 methylation could serve as a diagnostic biomarker and a potential therapeutic target for OOSCC metastasis.
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