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Proteomic Screening for Serum Biomarkers for Cervical Cancer and Their Clinical Significance

BACKGROUND: The present study aimed to determine serum markers for cervical cancer (CC) and to provide valuable references for clinical diagnosis and treatment. MATERIAL/METHODS: Serum samples were collected from age-matched healthy control women, and from female CC patients before and after surgery...

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Detalles Bibliográficos
Autores principales: Chen, Yani, Xiong, Xiaofan, Wang, Yanfeng, Zhao, Junmei, Shi, Haiyan, Zhang, Huahua, Wang, Yu, Wei, Yameng, Xue, Wanjuan, Zhang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6338008/
https://www.ncbi.nlm.nih.gov/pubmed/30625128
http://dx.doi.org/10.12659/MSM.911478
Descripción
Sumario:BACKGROUND: The present study aimed to determine serum markers for cervical cancer (CC) and to provide valuable references for clinical diagnosis and treatment. MATERIAL/METHODS: Serum samples were collected from age-matched healthy control women, and from female CC patients before and after surgery. Serum biomarkers were selected by comparing serum peptides profiles among the 3 groups by magnetic bead-based weak cation – exchange chromatography fractionation combined with matrix-assisted laser desorption/ionization-time of flight mass spectrometry. Probable serum biomarkers for cervical cancer were then further identified by liquid chromatography-electrospray ionization-tandem mass spectrometry system and the identified proteins were verified by enzyme-linked immunosorbent assay (ELISA). RESULTS: Three peptide biomarkers were identified for distinguishing CC patients from normal individuals, and distinguishing preoperative CC patients from postoperative CC patients. Of these 3 identified protein peptide regions, 2 peptide regions – TKT (Peak 2, 2435.63 m/z, 499–524) and FGA (Peak 4, 2761.79 m/z, 603–629) – were identified as upregulated markers, and peptide region of APOA1 (Peak 9, 2575.3 m/z, 245–260) was identified as a downregulated biomarker in preoperative CC patients compared with healthy women. CONCLUSIONS: The present study provides a new method for identifying potential serum biomarkers for CC patients.