Identifying Candidate Biomarkers for Pleomorphic Adenoma: A Case-Control Study.

Head Neck Pathol

Division of Oral and Maxillofacial Pathology, Department of Pathology and Laboratory Medicine, University of Western Ontario, 1151 Richmond Street, London, ON, N6A 5C1, Canada.

Published: September 2019

AI Article Synopsis

  • Pleomorphic adenoma (PA) is the most frequently occurring benign tumor in salivary glands, and the study investigates the expression of Kallikrein-related peptidases (KLKs) as potential biomarkers in these tumors.
  • Researchers analyzed fresh PA tissue from 26 specimens to assess KLK1-15 mRNA levels and corresponding protein expressions using advanced techniques, finding that KLK1, KLK12, and KLK13 were downregulated.
  • The research is significant as it is the first to map KLK expression profiles in PA, highlighting potential areas for future clinical applications based on these findings.

Article Abstract

Pleomorphic adenoma (PA) is the most common benign salivary gland tumor. Kallikrein-related peptidases have been identified as biomarkers in many human tumors and may influence tumor behavior. We investigated KLK1-15 messenger ribonucleic acid and proteins in PA specimens to determine a KLK expression profile for this tumor. Fresh frozen PA tissue specimens (n = 26) and matched controls were subjected to quantitative real-time reverse transcription polymerase chain reaction to detect KLK1-15 mRNA. Expression of KLK1, KLK12, KLK13, and KLK8 proteins were then evaluated via immunostaining techniques. Statistical analyses were performed with the level of significance set at P < .05. We observed downregulation of KLK1, KLK12, and KLK13 mRNA expression, and immunostaining studies revealed downregulation of the corresponding proteins. Histologic evidence of capsular perforation was associated with increased KLK1 protein expression. Tumor size was not associated with capsular invasion and/or perforation. This study is the first to detail a KLK expression profile for PA at both the transcriptional level and the protein level. Future work is required to develop clinical applications of these findings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684674PMC
http://dx.doi.org/10.1007/s12105-018-0959-6DOI Listing

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