2018
DOI: 10.1007/s00784-018-2777-3
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Identification of salivary metabolites for oral squamous cell carcinoma and oral epithelial dysplasia screening from persistent suspicious oral mucosal lesions

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Cited by 33 publications
(29 citation statements)
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“…A more recent study also found salivary metabolomics could separate lichen planus from oral cancer, finding discriminatory metabolites upregulated in oral cancer included indoleacetate, putrescine and phosphoethanolamine [51]. Oral cancer and precancerous dysplasia have also been separated from other clinically similar lesions including keratosis and inflammation [52].…”
Section: Current Knowledge Of the Salivary Metabolomementioning
confidence: 97%
“…A more recent study also found salivary metabolomics could separate lichen planus from oral cancer, finding discriminatory metabolites upregulated in oral cancer included indoleacetate, putrescine and phosphoethanolamine [51]. Oral cancer and precancerous dysplasia have also been separated from other clinically similar lesions including keratosis and inflammation [52].…”
Section: Current Knowledge Of the Salivary Metabolomementioning
confidence: 97%
“…Solo application of prospective sampling without blinded evaluation resulted in a high risk of bias in 62.5% of studies (Appendix B). The patient selection domain also had the greatest proportion of studies with high applicability concerns as a result of investigating biomarkers for the detection of OSCC recurrence or distant metastases, head and neck lymphomas, severe epithelial dysplasia, and metaplasia dyskeratosis in addition to primary OSCC diagnosis 17,18,21,22 …”
Section: Resultsmentioning
confidence: 99%
“…All studies reported that squamous carcinomas of the head and neck results in a higher serum l ‐fucose level than precancerous or healthy states; however, the sensitivity observed in the single study reporting quantitative measures of efficacy was moderate 19 . For salivary metabolomic biomarkers, Ishikawa and colleagues 22 suggested that the combination of ornithine, O ‐hydroxybenzoate, and ribose‐5‐phosphate had a high discriminatory power in delineating oral carcinomas and high‐grade oral dysplasia from other persistent suspicious oral mucosal lesions.…”
Section: Resultsmentioning
confidence: 99%
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“…In addition, the combination of priopionyl choline, N‐acetyl‐L‐phenylalanine, sphinganine, phytosphingosine and S‐carboxymethyl‐L‐cysteine also offer excellent sensitivity and specificity . Recent investigations have proposed altered levels of s‐adenosylmethionine + pipecolinic acid, and the combination of ornithine, o‐hydroxybenzoate and ribose‐5‐phosphate may be early diagnostic markers for OSCC . Other candidate markers such as lactate, proline, glycine, citrulline, inositol trisphosphate, 2‐oxoarginine and glycerate‐2‐phosphate have all been proposed as putative markers for future validation studies …”
Section: Metabolomic Biomarker Combinationsmentioning
confidence: 99%