4.7 Article

MicroRNA-137 Promoter Methylation Is Associated With Poorer Overall Survival in Patients With Squamous Cell Carcinoma of the Head And Neck

期刊

CANCER
卷 117, 期 7, 页码 1454-1462

出版社

WILEY
DOI: 10.1002/cncr.25689

关键词

miRNA; miR-137; epigenetics; prognosis; head and neck cancer

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资金

  1. American Cancer Society [RSG-05-246-01-GMC]
  2. National Institutes of Health [CA148629, CA132385, CA097190]
  3. Clinical and Translational Science Institute
  4. Institute for Clinical Research Education at the University of Pittsburgh [5TL1RR024155-03]

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BACKGROUND: The overall 5-year survival rate of approximately 60% for head and neck cancer patients has remained essentially unchanged over the past 30 years. MicroRNA-137 (miR-137) plays an essential role in cell-cycle control at the G1/S-phase checkpoint. However, the aberrant miR-137 promoter methylation observed in squamous cell carcinoma of the head and neck (SCCHN) suggests a tumor-specific molecular defect that may contribute to disease progression. METHODS: The goal of this study was to assess, in formalin-fixed, paraffin-embedded tumor tissue, the association between miR-137 promoter methylation and survival (both overall and disease free) and with prognostic factors including stage, tumor size, lymph node positivity, tumor grade, and surgical tumor margin positivity. RESULTS: The promoter methylation status of miR-137 was ascertained by methylation-specific polymerase chain reaction and detected in 11 of 67 SCCHN patients (16.4%), with no significant differences according to site (oral cavity, pharynx, larynx). Methylation of the miR-137 promoter was significantly associated with overall survival (hazard ratio, 3.68; 95% confidence interval, 1.01-13.38) but not with disease-free survival or any of the prognostic factors evaluated. CONCLUSIONS: The results of this study indicate that miR-137 is methylated in tumor tissue from pharyngeal and laryngeal squamous cancers, in addition to oral squamous cell carcinoma, and that miR-137 promoter methylation has potential utility as a prognostic marker for SCCHN. Cancer 2011; 117: 1454-62. (C) 2010 American Cancer Society.

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