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Immunohistochemical biomarkers in oral submucous fibrosis: A scoping review
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AbstractIntroductionThis scoping review was done to study the immunohistochemical biomarkers involved in the pathogenesis and malignant transformation of oral submucous fibrosis (OSF), in literature published from 2010 to 2021.MethodThe protocol was adapted from the Joanna Briggs Institute Reviewer's Manual (2017), and reported according to the PRISMA guidelines for Scoping Reviews.ResultsEighty‐six studies included in this review reported 84 immunohistochemical (IHC) biomarkers in OSF: 10 epithelial markers, 28 connective tissue markers, 22 proliferative markers, and 24 other biomarkers that are transcription factors, cancer stem cell markers, cell signaling markers, proteins, and enzymes. The commonly reported IHC biomarkers were alpha‐smooth muscle actin (α‐SMA) and E‐cadherin (seven articles each) followed by vascular endothelial growth factor (VEGF) and CD34 (six articles each), p53, p63, and Ki67 (five articles each). α‐SMA, Ki67, CD105, and hTERT were significantly increased in oral squamous cell carcinoma arising in a background of OSF (OSCC‐OSF) compared with OSF and normal subjects.ConclusionThe identified surrogate IHC biomarkers reported in OSF in this scoping review require validation with long‐term prospective studies to facilitate early diagnosis, for use in risk assessment, and plan appropriate treatment for OSF in clinical practice.Open Science Framework ID: osf.io/epwra
Title: Immunohistochemical biomarkers in oral submucous fibrosis: A scoping review
Description:
AbstractIntroductionThis scoping review was done to study the immunohistochemical biomarkers involved in the pathogenesis and malignant transformation of oral submucous fibrosis (OSF), in literature published from 2010 to 2021.
MethodThe protocol was adapted from the Joanna Briggs Institute Reviewer's Manual (2017), and reported according to the PRISMA guidelines for Scoping Reviews.
ResultsEighty‐six studies included in this review reported 84 immunohistochemical (IHC) biomarkers in OSF: 10 epithelial markers, 28 connective tissue markers, 22 proliferative markers, and 24 other biomarkers that are transcription factors, cancer stem cell markers, cell signaling markers, proteins, and enzymes.
The commonly reported IHC biomarkers were alpha‐smooth muscle actin (α‐SMA) and E‐cadherin (seven articles each) followed by vascular endothelial growth factor (VEGF) and CD34 (six articles each), p53, p63, and Ki67 (five articles each).
α‐SMA, Ki67, CD105, and hTERT were significantly increased in oral squamous cell carcinoma arising in a background of OSF (OSCC‐OSF) compared with OSF and normal subjects.
ConclusionThe identified surrogate IHC biomarkers reported in OSF in this scoping review require validation with long‐term prospective studies to facilitate early diagnosis, for use in risk assessment, and plan appropriate treatment for OSF in clinical practice.
Open Science Framework ID: osf.
io/epwra.
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