AI Article Synopsis

  • The study investigated methylation profiles in head and neck squamous-cell carcinoma (HNSCC) patients to assess their prognostic significance and potential as biomarkers.
  • Analysis involved qRT-PCR to examine gene expression and qMSP for promoter methylation on a sample set of 205 patients.
  • Findings indicated that promoter hypermethylation was linked to disease recurrence, showed strong diagnostic discrimination between cancerous and normal tissues, and correlated with decreased disease-free survival in early-stage patients, suggesting a role in HNSCC development and as a valuable biomarker.

Article Abstract

This study examined ( methylation profiles in head and neck squamous-cell carcinoma (HNSCC) patients at diagnosis and follow-up, and evaluated their prognostic significance and value as a biomarker. expression was examined in a panel of cell lines by quantitative reverse transcription PCR (qRT-PCR). Promoter methylation was determined by quantitative methylation-specific polymerase chain reaction (qMSP) and was compared to the clinical characteristics of 205 samples. promoter methylation was associated with transcriptional inhibition and was correlated with disease recurrence in 31.7% of cases, with an odds ratio of 1.694 (95% confidence interval: 1.093-2.626; P = 0.018) by multivariate Cox proportional hazard regression analysis. promoter hypermethylation showed highly discriminatory receiver operator characteristic curve profiles that clearly distinguished HNSCC from adjacent normal mucosal tissue, and was correlated with reduced disease-free survival in early stage T1 and T2 patients (log-rank test, P < 0.001). methylation was significantly correlated with the methylation status of both and . This study suggests that CpG hypermethylation is a likely mechanism of gene inactivation, supporting the hypothesis that might play a role in HNSCC tumorigenesis and could serve as an important biomarker.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868161PMC
http://dx.doi.org/10.7150/jca.23527DOI Listing

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