4.6 Article

Detection of serum/salivary exosomal Alix in patients with oral squamous cell carcinoma

Journal

ORAL DISEASES
Volume 27, Issue 3, Pages 439-447

Publisher

WILEY
DOI: 10.1111/odi.13565

Keywords

Alix; exosome; oral squamous cell carcinoma; tumor marker

Funding

  1. Japan Society for the Promotion of Science [26221304, JP17H04065, JP18K17025]
  2. Ministry of Education, Culture, Sports, Science and Technology: Nanotechnology Platform

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This study found that exosomal Alix levels in serum/saliva were significantly higher in patients with OSCC compared to healthy controls, indicating potential diagnostic biomarkers for OSCC. Serum exoAlix was also identified as suitable for predicting therapeutic responses.
Objective Owing to variations in the exterior appearances of noncancerous diseases in the oral cavity, clinicians may have difficulty diagnosing oral squamous cell carcinoma (OSCC). Tissue biopsy is confirmatory, but invasive. Therefore, reliable tumor markers for OSCC are required. Here, exosomal Alix (exoAlix) levels were measured in serum/salivary samples from patients with OSCC and healthy controls (HCs). Methods Fifty-seven patients admitted to Nagoya University Hospital from 2017 through 2019 were enrolled, and serum samples (OSCC,n = 29; HC,n = 21) and/or saliva samples (OSCC,n = 23; HC,n = 20) were collected. Exosomal fractions were isolated using ultracentrifugation. ExoAlix levels were measured using enzyme-linked immunosorbent assay. Results Serum/salivary exoAlix levels were significantly higher in patients with OSCC than in HCs. Receiver operating characteristic analyses revealed that sensitivity, specificity, positive predictive value, and area under the curve were 0.345, 1.000, 1.000, and 0.685, respectively, for serum exoAlix and 0.348, 1.000, 1.000, and 0.712, respectively, for salivary exoAlix at optimal cut-off values (serum, 0.205; saliva, 0.193). All tested OSCC tissue sections (n = 21) were immuno-reactive for Alix. Conclusion Serum and salivary exoAlix were identified as potential diagnostic OSCC biomarkers. Serum exoAlix was suitable for prediction of therapeutic responses.

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