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Tumor microRNA profile and prognostic value for lymph node metastasis in oral squamous cell carcinoma patients.
Liu, Kelly Yi Ping; Zhu, Sarah Yuqi; Brooks, Denise; Bowlby, Reanne; Durham, J Scott; Ma, Yussanne; Moore, Richard A; Mungall, Andrew J; Jones, Steven; Poh, Catherine F.
Affiliation
  • Liu KYP; Department of Oral Medical and Biological Sciences, Faculty of Dentistry, University of British Columbia, Vancouver, Canada.
  • Zhu SY; Department of Integrative Oncology, BC Cancer, Vancouver, Canada.
  • Brooks D; Department of Integrative Oncology, BC Cancer, Vancouver, Canada.
  • Bowlby R; Bioinformatics, Canada's Michael Smith Genome Sciences Center, Vancouver, Canada.
  • Durham JS; Bioinformatics, Canada's Michael Smith Genome Sciences Center, Vancouver, Canada.
  • Ma Y; Department of Surgery, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
  • Moore RA; Bioinformatics, Canada's Michael Smith Genome Sciences Center, Vancouver, Canada.
  • Mungall AJ; Faculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
  • Jones S; Biospecimen & Library Core Group, Canada's Michael Smith Genome Sciences Center, Vancouver, Canada.
  • Poh CF; Bioinformatics, Canada's Michael Smith Genome Sciences Center, Vancouver, Canada.
Oncotarget ; 11(23): 2204-2215, 2020 Jun 09.
Article in En | MEDLINE | ID: mdl-32577165
ABSTRACT
Neck lymph node metastasis (LN+) is one of the most significant prognostic factors affecting 1-in-2 patients diagnosed with oral squamous cell carcinoma (OSCC). The different LN outcomes between clinico-pathologically similar primary tumors suggest underlying molecular signatures that could be associated with the risk of nodal disease development. MicroRNAs (miRNAs)are short non-coding molecules that regulate the expression of their target genes to maintain the balance of cellular processes. A plethora of evidence has indicated that aberrantly expressed miRNAs are involved in cancers with either an antitumor or oncogenic role. In this study, we characterized miRNA expression among OSCC fresh-frozen tumors with known outcomes of nodal disease (82 LN+, 76 LN0). We identified 49 differentially expressed miRNAs in tumors of the LN+ group. Using penalized lasso Cox regression, we identified a group of 10 miRNAs of which expression levels were highly associated with nodal-disease free survival. We further reported a 4-miRNA panel (miR-21-5p, miR-107, miR-1247-3p, and miR-181b-3p) with high accuracy in discriminating LN status, suggesting their potential application as prognostic biomarkers for nodal disease.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Oncotarget Year: 2020 Document type: Article Affiliation country: Canadá

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Oncotarget Year: 2020 Document type: Article Affiliation country: Canadá