RAB25 expression is epigenetically downregulated in oral and oropharyngeal squamous cell carcinoma with lymph node metastasisClausen, M. J. A. M., Melchers, L. J., Mastik, M. F., Slagter-Menkema, L., Groen, H. J. M., van der Laan, B. F. A. M., van Criekinge, W., de Meyer, T., Denil, S., van der Vegt, B., Wisman, G. B. A., Roodenburg, J. L. N. & Schuuring, E., 2016, In : Epigenetics. 11, 9, p. 653-663 11 p.
Research output: Contribution to journal › Article › Academic › peer-review
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.
|Number of pages||11|
|Publication status||Published - 2016|
- DNA methylation, epigenetic regulation, head and neck cancer, metastasis, MethylCap-Seq, oral squamous cell carcinoma, NECK-CANCER, DIFFERENTIAL EXPRESSION, PROMOTER METHYLATION, BREAST-CANCER, HEAD, GENE, IDENTIFICATION, VALIDATION, MICROARRAY, PREDICTION