Downregulation of miRNA-424: a sign of field cancerisation in clinically normal tongue adjacent to squamous cell carcinoma

L. Boldrup (Lead / Corresponding author), P. J. Coates, G. Laurell, T. Wilms, R. Fahraeus, K. Nylander

    Research output: Contribution to journalArticlepeer-review

    32 Citations (Scopus)

    Abstract

    Background: The overall survival for patients with squamous cell carcinoma of the tongue is low and the search for early diagnostic and prognostic markers is thus essential. MicroRNAs have been suggested as potential prognostic and diagnostic candidates in squamous cell carcinoma of head and neck in general.

    Methods: On the basis of the known differences between sub-sites within the oral cavity, we investigated the expression and role of microRNA-424 in squamous cell carcinoma arising in tongue. MicroRNA levels were measured by qRT-PCR in both tissue and plasma samples.

    Results: Levels of microRNA-424 were upregulated in tongue squamous cell carcinoma, but not in tumours originating from gingiva or floor of the mouth. Interestingly, microRNA-424 was downregulated in clinically normal tongue tissue next to tumour compared with completely healthy tongue, indicating that microRNA-424 could be a marker of field cancerisation in this tumour type. However, expression of microRNA-424 in a tongue-derived epithelial cell line revealed no significant changes in the expression profile of proteins and genes.

    Conclusions: Our patient data show that microRNA-424 alterations are a marker of field cancerisation specific for tongue tumourigenesis, which also could have a role in development of tongue squamous cell carcinoma.

    Original languageEnglish
    Pages (from-to)1760-1765
    Number of pages6
    JournalBritish Journal of Cancer
    Volume112
    Issue number11
    Early online date12 May 2015
    DOIs
    Publication statusPublished - 26 May 2015

    Keywords

    • Field cancerisation
    • miRNA
    • miRNA-424
    • Tongue SCC

    ASJC Scopus subject areas

    • Cancer Research
    • Oncology

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