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Chairside molecular imaging of aberrant glycosylation in subjects with suspicious oral lesions using fluorescently labeled wheat germ agglutinin
Author(s) -
Baeten John,
Johnson Alexander,
Sunny Sumsum,
Suresh Amritha,
Birur Praveen,
Uma K,
Kademani Deepak
Publication year - 2018
Publication title -
head and neck
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.012
H-Index - 127
eISSN - 1097-0347
pISSN - 1043-3074
DOI - 10.1002/hed.24943
Subject(s) - wheat germ agglutinin , pathology , fluorescein isothiocyanate , in vivo , medicine , agglutinin , sialic acid , fluorescein , fluorescence , biology , lectin , biochemistry , immunology , physics , microbiology and biotechnology , quantum mechanics
Abstract Background Aberrant sialylation is accepted as a carcinogenic biomarker. In previous work, fluorescently labeled wheat germ agglutinin (WGA) distinguished between cancerous and normal oral biopsies. The purpose of this study was to investigate WGA‐fluorescein isothiocyanate (FITC) as a point‐of‐care tool for detecting oral malignant and dysplastic lesions in vivo. Methods Subject recruitment was divided into two groups: (1) the clinically normal oral mucosa group; or (2) the presence of clinically suspicious oral lesion(s) group. A WGA‐FITC solution was topically applied to observable lesions or to half the subject's mouth (sagittal plane) if lesions were absent. Fluorescent molecular imaging was used to evaluate WGA‐FITC localization. Results Fluorescent imaging in 55 subjects demonstrated that WGA‐FITC could detect histopathologically‐confirmed cancerous and dysplastic lesions with high sensitivity (100% and 81%, respectively) and specificity (82%). Conclusion This study supports in vivo fluorescent molecular imaging of WGA‐FITC to visualize aberrant sialic acid expression associated with carcinogenesis. This technique resulted in the immediate chairside detection of oral cancerous and dysplastic lesions.