Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/68519
標題: Salivary zinc finger protein 510 peptide as a novel biomarker for detection of oral squamous cell carcinoma in early stages
作者: Jou, Y.J.
Lin, C.D.
Lai, C.H.
Tang, C.H.
Huang, S.H.
Tsai, M.H.
Chen, S.Y.
Kao, J.Y.
Lin, C.W.
關鍵字: Oral squamous cell carcinoma;Biomarkers;Matrix-assisted laser;desorption/ionization time-of-flight;Zinc finger protein 510;ClinProt;neck-cancer;diagnosis;znf652;head
Project: Clinica Chimica Acta
期刊/報告no:: Clinica Chimica Acta, Volume 412, Issue 15-16, Page(s) 1357-1365.
摘要: 
Background: Oral squamous cell carcinoma (OSCC) is one of the most frequent malignancies worldwide. Early diagnosis can mean adequate treatment and increase survival. Methods: This study uses ClinProt technique to identify salivary biomarkers for early diagnosis of OSCC. A total of 77 salivary samples from both OSCC patients (n = 47) and healthy donors (n = 30) were analyzed with MALDI-TOF MS technology. Results: Salivary peptides from OSCC patients were separated, using C8-functionalized magnetic beads. Three signals (2918.57 Da, 5592.64 Da, and 4372.66 Da) distinguished OSCC patients from controls. Among them, unique peptide 2918.57 Da, identified as a 24-mer peptide of zinc finger protein 510 (ZNF510). was found in 0% of saliva from healthy individuals, versus 25.0% and 60% from OSCC patients with T1 + T2 and T3 + T4 stages, respectively (P < 0.001). ELISA analysis with rabbit anti-ZNF510 peptide sera shows a starkly higher 24-mer ZNF510 peptide level in saliva from OSCC patients than that in controls (P<0.001). Also, in immunohistochemical analysis of oral tissues, a significantly higher level of ZNF510 was observed in OSCC tissues than in the OSCC free control tissues. Analysis of areas under receiver-operating characteristic (ROC) curves in OSCC early (T1 + T2) and late stages (T3 + T4) shows greater than 0.95. Conclusions: Identifying 24-met ZNF510 peptide as OSCC-related salivary biomarkers via proteomic approach proved useful in adjunct diagnosis for early detection rather than specific diagnosis marker for progression of OSCC patients. (C) 2011 Elsevier B.V. All rights reserved.
URI: http://hdl.handle.net/11455/68519
ISSN: 0009-8981
DOI: 10.1016/j.cca.2011.04.004
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