Comparative analysis of micro-RNAs in human papillomavirus-positive versus -negative oropharyngeal cancers

Head Neck. 2016 Nov;38(11):1634-1642. doi: 10.1002/hed.24487. Epub 2016 Apr 21.

Abstract

Background: Oncogenic mechanisms of human papillomavirus (HPV)-positive oropharyngeal cancer are still poorly characterized. Analysis of their microRNA expression profile might provide valuable information.

Methods: The microRNA expression profiles were analyzed by micro-arrays in 26 oropharyngeal cancers. A microRNA signature specific to HPV-status was identified by analyzing a learning/training set consisting of 16 oropharyngeal cancers. The robustness of this signature was further confirmed by blind case-by-case classification of a validation set composed of 10 independent tumors. Putative targeted molecular pathways were proposed using DIANA miRPath online software (http://microrna.gr/mirpath).

Results: We have identified 25 miRNA signatures, which discriminates HPV16-positive oropharyngeal cancer from their HPV-negative counterparts. These 25 microRNAs play a potential role in Wnt and PI3K-pathways, cell-adhesion/cell-polarity, and the cytoskeleton regulation.

Conclusion: Our study contributes to a better understanding of pathogenic mechanisms involved in the development of HPV-positive oropharyngeal cancer and in the identification of potential therapeutic molecular targets. © 2016 Wiley Periodicals, Inc. Head Neck 38: 1708-1716, 2016.

Keywords: PI3K pathway; Wnt pathway; gene expression profile; human papillomavirus 16; micro/miRNA; microarray; oropharyngeal/oropharynx cancer.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / virology
  • Female
  • Human papillomavirus 16 / isolation & purification
  • Humans
  • Male
  • MicroRNAs / metabolism*
  • Middle Aged
  • Oropharyngeal Neoplasms / genetics*
  • Oropharyngeal Neoplasms / virology
  • Papillomavirus Infections / complications
  • Sequence Analysis, RNA
  • Transcriptome

Substances

  • MicroRNAs