Low-Level Expression of miR-375 Correlates with Poor Outcome and Metastasis While Altering the Invasive Properties of Head and Neck Squamous Cell Carcinomas
Small, noncoding microRNAs (miRNAs) have been shown to be abnormally expressed in every tumor type examined. We used comparisons of global miRNA expression profiles of head and neck squamous cell carcinoma (HNSCC) samples and adjacent normal tissue to rank those miRNAs that were most significantly altered in our patient population. Rank Consistency Score analysis revealed miR-375 to have the most significantly lowered miRNA levels in tumors relative to matched adjacent nonmalignant tissue from the same patient among 736 miRNAs that were evaluated. This result has been previously observed by other groups; however, we extend this finding with the unique observation that low miR-375 expression levels correlate significantly with cancer survival and distant metastasis. In a study of 123 primary HNSCC patients using multivariable Cox proportional hazard ratios (HR) and 95% confidence intervals (CI), both death from disease (HR: 12.8, 95% CI: 3 to 49) and incidence of distant metastasis (HR: 8.7, 95% CI: 2 to 31) correlated with lower expression levels of miR-375 regardless of the site or stage of the tumor. In addition, we found that oral cavity tumor cell lines (eg, UMSCC1 and UMSCC47) overexpressing miR-375 were significantly less invasive in vitro than their matched empty vector controls. We conclude that miR-375 represents a potential prognostic marker of poor outcome and metastasis in HNSCC and that it may function by suppressing the tumor's invasive properties.
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Supported in part by funds from the Department of Pathology, Albert Einstein College of Medicine and Montefiore Medical Center and by grants from the National Institutes of Health (CA77522 and CA100324 to J.E.S.). J.E.S. is the Betty and Sheldon Feinberg Senior Faculty Scholar in Cancer Research.
T.H. and L.J. contributed equally to this work. G.C. and J.E.S. are co-contributing authors.
Supplemental material for this article can be found at http://ajp.amjpathol.org or at doi: 10.1016/j.ajpath.2011.12.004
A guest editor acted as editor-in-chief for the manuscript. No person at Albert Einstein College of Medicine or Thomas Jefferson University was involved in the peer review process or final disposition of this article.
PII: S0002-9440(11)01094-7
doi:10.1016/j.ajpath.2011.12.004
© 2012 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.
