MiR-21 expression in the tumor stroma of oral squamous cell carcinoma: an independent biomarker of disease free survival

PLoS One. 2014 Apr 22;9(4):e95193. doi: 10.1371/journal.pone.0095193. eCollection 2014.

Abstract

Oral squamous cell carcinoma (OSCC) patients have a high mortality rate; thus, new clinical biomarkers and therapeutic options are needed. MicroRNAs (miRNAs) are short noncoding RNAs that regulate posttranscriptional gene expression and are commonly deregulated in OSCC and other cancers. MicroRNA-21 (miR-21) is the most consistently overexpressed miRNA in several types of cancer, and it might be a useful clinical biomarker and therapeutic target. To better understand the role of miR-21 in OSCC, paraffin-embedded tumor tissue samples from 86 patients with primary OSCC were analyzed by in situ hybridization. We found that miR-21 was primarily expressed in the tumor stroma and in some tumor-associated blood vessels with no expression in the adjacent normal epithelia or stroma. Using image analysis, we quantitatively estimated miR-21 expression levels specifically in the stroma of a cohort of OSCC samples. These miR-21 levels significantly correlated with disease free survival with the highest levels being located in the stroma. Stromal miR-21 expression was independently associated with a poorer prognosis, even after adjusting for clinical parameters (perineural invasion and N-stage) in a multivariate analysis. In summary, we have shown that miR-21 is located in the carcinoma cells, stroma and blood vessels of tumors, and its expression specifically in the stromal compartment has a negative prognostic value in OSCC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acinar Cells / metabolism
  • Acinar Cells / pathology
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / metabolism
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / pathology
  • Disease-Free Survival
  • Endothelium / metabolism
  • Endothelium / pathology
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Image Processing, Computer-Assisted
  • In Situ Hybridization
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Mouth Neoplasms / genetics*
  • Mouth Neoplasms / pathology
  • Multivariate Analysis
  • Myofibroblasts / metabolism
  • Myofibroblasts / pathology
  • Statistics, Nonparametric
  • Stromal Cells / metabolism
  • Stromal Cells / pathology

Substances

  • Biomarkers, Tumor
  • MIRN21 microRNA, human
  • MicroRNAs

Grants and funding

David H. Jensen is supported by a grant from the non-profit foundation Candys Foundation. Erik Dabelsteen is supported by a grant from the Fredheim Stiftung. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.