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Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma

Oral cavity squamous cell carcinoma (OSCC) is a destructive disease with increasing incidence. OSCC is usually diagnosed at an advanced stage, which leads to poor outcomes of OSCC patients. Currently, there is a lack of biomarkers with sufficient effectiveness in early diagnosis of OSCC. To ameliora...

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Autores principales: Hsueh, Pei-Chun, Chang, Kai-Ping, Liu, Hao-Ping, Chiang, Wei-Fan, Chan, Xiu-Ya, Hung, Chu-Mi, Chu, Lichieh Julie, Wu, Chih-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659860/
https://www.ncbi.nlm.nih.gov/pubmed/36387116
http://dx.doi.org/10.3389/fonc.2022.968570
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author Hsueh, Pei-Chun
Chang, Kai-Ping
Liu, Hao-Ping
Chiang, Wei-Fan
Chan, Xiu-Ya
Hung, Chu-Mi
Chu, Lichieh Julie
Wu, Chih-Ching
author_facet Hsueh, Pei-Chun
Chang, Kai-Ping
Liu, Hao-Ping
Chiang, Wei-Fan
Chan, Xiu-Ya
Hung, Chu-Mi
Chu, Lichieh Julie
Wu, Chih-Ching
author_sort Hsueh, Pei-Chun
collection PubMed
description Oral cavity squamous cell carcinoma (OSCC) is a destructive disease with increasing incidence. OSCC is usually diagnosed at an advanced stage, which leads to poor outcomes of OSCC patients. Currently, there is a lack of biomarkers with sufficient effectiveness in early diagnosis of OSCC. To ameliorate OSCC screening, we evaluated the performances of salivary autoantibodies (auto-Abs) to nine proteins (ANXA2, CA2, ISG15, KNG1, MMP1, MMP3, PRDX2, SPARC, and HSPA5) as OSCC biomarkers. A multiplexed immunoassay using a fluorescence bead-based suspension array system was established for simultaneous assessment of the salivary levels of the above nine auto-Abs and a known OSCC-associated auto-Ab, anti-p53. Compared to healthy individuals (n = 140), the salivary levels of nine auto-Abs were significantly elevated in OSCC patients (n = 160). Notably, the salivary levels of the 10 auto-Abs in the early-stage OSCC patients (n = 102) were higher than that in the healthy group. Most importantly, utilizing a marker panel consisting of anti-MMP3, anti-PRDX2, anti-SPARC, and anti-HSPA5 for detection of early-stage OSCC achieved a sensitivity of 63.8% with a specificity of 90%. Collectively, herein we established a multiplex auto-Ab platform for OSCC screening, and demonstrated a four-auto-Ab panel which shows clinical applicability for early diagnosis of OSCC.
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spelling pubmed-96598602022-11-15 Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma Hsueh, Pei-Chun Chang, Kai-Ping Liu, Hao-Ping Chiang, Wei-Fan Chan, Xiu-Ya Hung, Chu-Mi Chu, Lichieh Julie Wu, Chih-Ching Front Oncol Oncology Oral cavity squamous cell carcinoma (OSCC) is a destructive disease with increasing incidence. OSCC is usually diagnosed at an advanced stage, which leads to poor outcomes of OSCC patients. Currently, there is a lack of biomarkers with sufficient effectiveness in early diagnosis of OSCC. To ameliorate OSCC screening, we evaluated the performances of salivary autoantibodies (auto-Abs) to nine proteins (ANXA2, CA2, ISG15, KNG1, MMP1, MMP3, PRDX2, SPARC, and HSPA5) as OSCC biomarkers. A multiplexed immunoassay using a fluorescence bead-based suspension array system was established for simultaneous assessment of the salivary levels of the above nine auto-Abs and a known OSCC-associated auto-Ab, anti-p53. Compared to healthy individuals (n = 140), the salivary levels of nine auto-Abs were significantly elevated in OSCC patients (n = 160). Notably, the salivary levels of the 10 auto-Abs in the early-stage OSCC patients (n = 102) were higher than that in the healthy group. Most importantly, utilizing a marker panel consisting of anti-MMP3, anti-PRDX2, anti-SPARC, and anti-HSPA5 for detection of early-stage OSCC achieved a sensitivity of 63.8% with a specificity of 90%. Collectively, herein we established a multiplex auto-Ab platform for OSCC screening, and demonstrated a four-auto-Ab panel which shows clinical applicability for early diagnosis of OSCC. Frontiers Media S.A. 2022-10-31 /pmc/articles/PMC9659860/ /pubmed/36387116 http://dx.doi.org/10.3389/fonc.2022.968570 Text en Copyright © 2022 Hsueh, Chang, Liu, Chiang, Chan, Hung, Chu and Wu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Hsueh, Pei-Chun
Chang, Kai-Ping
Liu, Hao-Ping
Chiang, Wei-Fan
Chan, Xiu-Ya
Hung, Chu-Mi
Chu, Lichieh Julie
Wu, Chih-Ching
Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma
title Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma
title_full Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma
title_fullStr Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma
title_full_unstemmed Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma
title_short Development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma
title_sort development of a salivary autoantibody biomarker panel for diagnosis of oral cavity squamous cell carcinoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659860/
https://www.ncbi.nlm.nih.gov/pubmed/36387116
http://dx.doi.org/10.3389/fonc.2022.968570
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