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Identification of serum biomarkers for occupational medicamentosa-like dermatitis induced by trichloroethylene using mass spectrometry.

Authors :
Hong, Wen-Xu
Liu, Wei
Zhang, Yanfang
Huang, Peiwu
Yang, Xifei
Ren, Xiaohu
Ye, Jinbo
Huang, Haiyan
Tang, Haiyan
Zhou, Guifeng
Huang, Xinfeng
Zhuang, Zhixiong
Liu, Jianjun
Source :
Toxicology & Applied Pharmacology. Nov2013, Vol. 273 Issue 1, p121-129. 9p.
Publication Year :
2013

Abstract

Abstract: Occupational medicamentosa-like dermatitis induced by trichloroethylene (OMLDT) is an autoimmune disease and it has become a serious occupational health hazard. In the present study, we collected fasting blood samples from patients with OMLDT (n=18) and healthy volunteers (n=33) to explore serum peptidome patterns. Peptides in sera were purified using weak cation exchange magnetic beads (MB-WCX), and analyzed by matrix-assisted laser desorption ionization time-of-flight-mass spectrometry (MALDI-TOF-MS) and ClinProTools bioinformatics software. The intensities of thirty protein/peptide peaks were significantly different between the healthy control and OMLDT patients. A pattern of three peaks (m/z 2106.3, 2134.5, and 3263.67) was selected for supervised neural network (SNN) model building to separate the OMLDT patients from the healthy controls with a sensitivity of 95.5% and a specificity of 73.8%. Furthermore, two peptide peaks of m/z 4091.61 and 4281.69 were identified as fragments of ATP-binding cassette transporter family A member 12 (ABCA12), and cationic trypsinogen (PRRS1), respectively. Our findings not only show that specific proteomic fingerprints in the sera of OMLDT patients can be served as a differentiated tool of OMLDT patients with high sensitivity and high specificity, but also reveal the novel correlation between OMLDT with ABC transports and PRRS1, which will be of potential value for clinical and mechanistic studies of OMLDT. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
0041008X
Volume :
273
Issue :
1
Database :
Academic Search Index
Journal :
Toxicology & Applied Pharmacology
Publication Type :
Academic Journal
Accession number :
91921235
Full Text :
https://doi.org/10.1016/j.taap.2013.08.014