Oral Oncology
Volume 46, Issue 3 , Pages 204-208, March 2010

miR-24 up-regulation in oral carcinoma: Positive association from clinical and in vitro analysis

  • Shu-Chun Lin

      Affiliations

    • School of Dentistry, National Yang-Ming University, Taipei, Taiwan
  • ,
  • Chung-Ji Liu

      Affiliations

    • School of Dentistry, National Yang-Ming University, Taipei, Taiwan
    • Oral and Maxillofacial Surgery, MacKay Memorial Hospital, Taipei, Taiwan
  • ,
  • Jung-An Lin

      Affiliations

    • School of Dentistry, National Yang-Ming University, Taipei, Taiwan
  • ,
  • Wei-Fan Chiang

      Affiliations

    • School of Dentistry, National Yang-Ming University, Taipei, Taiwan
    • Department of Dentistry, Chimei Hospital, Liouying Campus, Tainan, Taiwan
  • ,
  • Pei-Shih Hung

      Affiliations

    • School of Dentistry, National Yang-Ming University, Taipei, Taiwan
  • ,
  • Kuo-Wei Chang

      Affiliations

    • School of Dentistry, National Yang-Ming University, Taipei, Taiwan
    • Department of Stomatology, Veterans General Hospital, Taipei, Taiwan
    • Corresponding Author InformationCorresponding author. Address: School of Dentistry, National Yang-Ming University, Beitou, Taipei 112, Taiwan. Tel.: +886 2 28267223; fax: +886 2 28264053.

Received 1 December 2009; received in revised form 16 December 2009; accepted 17 December 2009. published online 08 February 2010.

Summary 

MicroRNAs (miRNAs) play important roles in neoplastic process. miR-24 is localized on chromosome 9q22 and 19p13, regions frequently altered in oral squamous cell carcinoma (OSCC). This study showed that miR-24 was up-regulated in OSCC tissues relative to control samples. In addition, the plasma levels of miR-24 in OSCC patients were significantly higher than in control individuals. miR-24 expression was also higher in OSCC cell lines relative to normal oral keratinocytes. Experiments blocking miR-24 and using exogenous miR-24 expression indicated that miR-24 contributes to the growth of OSCC cells and that miR-24 may target p57. This study suggests that miR-24 is involved in the regulation of OSCC growth and that the miR-24’s level in plasma may be validatable as a tumor marker for OSCC patients.

Keywords: Carcinoma, MicroRNA, Oral cavity, Plasma, Proliferation, miR-24

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PII: S1368-8375(09)01010-0

doi:10.1016/j.oraloncology.2009.12.005

Oral Oncology
Volume 46, Issue 3 , Pages 204-208, March 2010