4.7 Article

Improving the diagnostic efficacy of squamous cell carcinoma antigen for oral squamous cell carcinoma via saponin disruption of serum extracellular vesicles

Journal

CLINICA CHIMICA ACTA
Volume 525, Issue -, Pages 40-45

Publisher

ELSEVIER
DOI: 10.1016/j.cca.2021.12.012

Keywords

Squamous cell carcinoma antigen; Oral squamous cell carcinoma; Saponin; Extracellular vesicles

Funding

  1. National Natural Science Founda-tion of China [81803088, 81870762]
  2. Medical and Engineering Cross Research Foundation of Shanghai Jiao Tong University [YG2016QN15]
  3. Shanghai Sailing Program [19YF1427500]

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By using saponin to disrupt the membranes of serum EVs, the diagnostic efficacy of SCCA for oral squamous cell carcinoma can be improved. This provides a simple and rapid method with great potential for clinical application.
Background: The diagnostic value of squamous cell carcinoma antigen (SCCA) for oral squamous cell carcinoma (OSCC) is insufficient. Recently, extracellular vesicles (EVs) have displayed great potential for improving diagnostic efficacy. However, one of the main challenges that restricts the application of EVs is the lack of a clinically suitable separation method for the intra-vesicular protein detection.Methods: Saponin was used to destroy serum EVs membranes for releasing the intra-vesicular SCCA into the serum, circumventing the purification process of EVs. The concentrations of SCCA were measured and compared in 113 healthy people and 73 OSCC patients pre-and post-saponin treatment.Results: The concentration of serum SCCA significantly increased after saponin destroyed the membrane of EVs. The area under the curve (AUC) of serum SCCA for OSCC diagnosis was 0.6444 (95% CI, 0.5595 to 0.7293). The diagnostic AUC of serum EVs-derived SCCA reached 0.7969 (95% CI, 0.735 to 0.8588).Conclusions: The results suggested that serum EVs disrupted by saponin could improve the diagnostic efficacy of SCCA for OSCC, which provides a simple, rapid, and high-throughput method to detect the intra-vesicular proteins of EVs and holds great potential for clinical application.

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