ArticleClinical oral investigations2011
MAGE-A antigens in lesions of the oral mucosa.
Article in Clinical oral investigations, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 19 citations in OpenAlex.
- Effectiveness of autofluorescence to identify suspicious oral lesions--a prospective, blinded clinical trial.Clinical oral investigations · 2011Trial
- Review
- Malignant transformation of oral leukoplakia is associated with macrophage polarization.Journal of translational medicine · 2020Article
- MAGE-A expression in oral and laryngeal leukoplakia predicts malignant transformation.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2019Article
- MAGE-A9 in head and neck cancer: Prognostic value and preclinical findings in the context of irradiation.Molecular and clinical oncology · 2018Article
- The prognostic value of GLUT-1 staining in the detection of malignant transformation in oral mucosa.Clinical oral investigations · 2017Article
- Contrary melanoma-associated antigen-A expression at the tumor front and center: A comparative analysis of stage I and IV head and neck squamous cell carcinoma.Oncology letters · 2016Article
- Melanoma-associated antigen expression and the efficacy of tyrosine kinase inhibitors in head and neck cancer.Oncology letters · 2015Article
- Correlation of MAGE-A tumor antigens and the efficacy of various chemotherapeutic agents in head and neck carcinoma cells.Clinical oral investigations · 2014Article
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Authors and funding
8 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Oral squamous cell carcinoma develops continuously out of predamaged oral mucosa. For the physician and pathologist, difficulties arise in distinguishing precancerous from cancerous lesions. MAGE-A antigens are tumor antigens that are found solely in malignant transformed cells. These antigens might be useful in distinguishing precancerous from cancerous lesions. The aim of this study was to verify this assumption by comparing MAGE-A expression in benign, precancerous, and cancerous lesions of the oral mucosa. Retrospectively, biopsies of different oral lesions were randomly selected. The lesions that were included are 64 benign oral lesions (25 traumatic lesions (oral ulcers), 13 dental follicles, and 26 epulis), 26 oral lichen planus, 123 epithelial precursor lesions (32 epithelial hyperplasia found in leukoplakias, 24 epithelial dysplasia found in leukoplakias, 26 erythroplasia with oral epithelial dysplasia, and 41 carcinomas in situ in erythroleukoplakias). The lesions were immunohistochemically stained with the poly-MAGE-A antibody 57B, and the results were compared. Biopsies of oral lichen planus, oral ulcers, dental follicles, epulis, and leukoplakia without dysplasia showed no positive staining for MAGE-A antigens. Leukoplakia with dysplasia, dysplasia, and carcinomata in situ displayed positive staining in 33%, 65%, and 56% of the cases, respectively. MAGE-A antigens were not detectable via immunohistochemistry in benign lesions of the oral mucosa. The staining rate of dysplastic precancerous lesions or malignant lesions ranged from 33% to 65%. The MAGE-A antigens might facilitate better differentiation between precancerous and cancerous lesions of the oral mucosa.
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