Proteomics-based identification of plasma biomarkers in oral squamous cell carcinoma

被引:34
|
作者
Tung, Chun-Liang [1 ,2 ]
Lin, Szu-Ting [3 ,4 ]
Chou, Hsiu-Chuan [5 ]
Chen, Yi-Wen [3 ,4 ]
Lin, Hwan-Chung [6 ]
Tung, Chung-Liang [6 ]
Huang, Kao-Jean [7 ,8 ]
Chen, Yi-Ju [1 ]
Lee, Ying-Ray [9 ,10 ]
Chan, Hong-Lin [3 ,4 ]
机构
[1] Chiayi Christian Hosp, Dept Pathol, Chiayi, Taiwan
[2] Chang Gung Univ Sci & Technol, Dept Nursing, Chiayi, Taiwan
[3] Natl Tsing Hua Univ, Inst Bioinformat & Struct Biol, Hsinchu 30013, Taiwan
[4] Natl Tsing Hua Univ, Dept Med Sci, Hsinchu 30013, Taiwan
[5] Natl Hsinchu Univ Educ, Dept Appl Sci, Hsinchu, Taiwan
[6] Chiayi Christian Hosp, Dept Oral & Maxillofacial Surg, Chiayi, Taiwan
[7] Natl Dong Hwa Univ, Dept Life Sci, Hualien, Taiwan
[8] Natl Dong Hwa Univ, Inst Biotechnol, Hualien, Taiwan
[9] Chiayi Christian Hosp, Dept Med Res, Chiayi, Taiwan
[10] Min Hwei Coll Hlth Care Management, Dept Nursing, Tainan, Taiwan
关键词
Oral squamous cell carcinoma; 2D-DIGE; Proteomic; Biomarker; Plasma; DIFFERENCE GEL-ELECTROPHORESIS; OXIDATIVE STRESS; ACTIVE-SITE; IN-VIVO; CANCER; CYSTEINE; PEROXIREDOXINS; OVEROXIDATION; TAIWAN; GROWTH;
D O I
10.1016/j.jpba.2012.11.017
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Oral squamous cell carcinoma (OSCC) is an aggressive cancer and its occurrence is closely related to betel nut chewing in Taiwan. However, there are few prognostic and diagnostic biomarkers for this disease especially for its association with betel nut chewing. Recent progresses in quantitative proteomics have offered opportunities to discover plasma proteins as biomarkers for tracking the progression and for understanding the molecular mechanisms of OSCC. In present study, plasma samples from OSCC patients with at least 5-year history of betel nut chewing and healthy donors were analyzed by fluorescence 2D-DIGE-based proteomic analysis. Totally, 38 proteins have been firmly identified representing 13 unique gene products. These proteins mainly function in inflammatory responses (such as fibrinogen gamma chain) and transport (Apolipoprotein A-I). Additionally, the current quantitative proteomic approach has identified numerous OSCC biomarkers including fibrinogen (alpha/beta/gamma) chain, haptoglobin, leucine-rich alpha-2-glycoprotein and ribosomal protein S6 kinase alpha-3 (RSK2) which have not been reported and may be associated with the progression and development of the disease. In summary, this study reports a comprehensive patient-based proteomic approach for the identification of potential plasma biomarkers in OSCC. The potential of utilizing these markers for screening and treating OSCC warrants further investigations. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 17
页数:11
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