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Low-level expression of miR-375 correlates with poor outcome and metastasis while altering the invasive properties of head and neck squamous cell carcinomas.

Thomas Harris | Lizandra Jimenez | Nicole Kawachi | Jian-Bing Fan | Jing Chen | Tom Belbin | Andrew Ramnauth | Olivier Loudig | Christian E Keller | Richard Smith | Michael B Prystowsky | Nicolas F Schlecht | Jeffrey E Segall | Geoffrey Childs
The American journal of pathology | 2012

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.

Pubmed ID: 22234174

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: P01 CA100324
  • Agency: NCI NIH HHS, United States
    Id: CA100324
  • Agency: NCI NIH HHS, United States
    Id: R01 CA077522
  • Agency: NCI NIH HHS, United States
    Id: F31 CA168337
  • Agency: NCI NIH HHS, United States
    Id: CA77522

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