Title of article
LAMP3 (CD208) Expression in Squamous Cell Carcinoma and Epithelial Dysplasia of the Oral Cavity and Clinicopathological Characteristics of Unfavorable Prognosis
Author/Authors
Shahabinejad, Mehdi Department of Oral and Maxillofacial Pathology - School of Dentistry - Mashhad University of Medical Sciences, Mashhad, Iran , Zare, Reza Oral and Maxillofacial Diseases Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Asadi, Zeynab Dental Research Center - Mashhad University of Medical Sciences, Mashhad, Iran , Mohajertehran, Farnaz Department of Oral and Maxillofacial Pathology - School of Dentistry - Mashhad University of Medical Sciences, Mashhad, Iran - Oral and Maxillofacial Diseases Research Center - Mashhad University of Medical Sciences, Mashhad, Iran
Pages
6
From page
373
To page
378
Abstract
Background: This study aimed to evaluate LAMP3 (CD208) gene expression in oral squamous cell carcinoma (OSCC) and dysplastic oral epithelium by quantitative real-time polymerase chain reaction (qPCR) and compare LAMP3 expression in different disease grades and stages.
Methods: In this study, 60 OSCC and dysplastic oral epithelium samples were obtained from the Mashhad
University of Medical Sciences together with their demographic and clinicopathological documents. LAMP3
expression was measured by qPCR.
Results: LAMP3 expression was significantly greater in OSCC than in dysplasia samples (P=0.001), in grade
III OSCC than in grades I and II, and also greater in advanced than in early OSCC disease stage (P=0.001).
Conclusions: The significantly greater LAMP3 expression in OSCC than in dysplastic epithelium indicates a
role for LAMP3 in carcinogenesis in oral mucosa. Our results suggest LAMP3 may be useful as an anticancer target and/or to predict disease pathogenesis in OSCC patient’s cells.
Keywords
Clinicopathological , Grade , Epithelial dysplasia , LAMP3 , Stage , Squamous cell carcinoma
Journal title
Reports of Biochemistry and Molecular Biology (RBMB)
Serial Year
2021
Record number
2720248
Link To Document