Apurinic/Apyrimidinic Endonuclease 1/Redox Factor-1 Could Serve as a Potential Serological Biomarker for the Diagnosis and Prognosis of Oral Squamous Cell Carcinoma.


Journal

Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
ISSN: 1531-5053
Titre abrégé: J Oral Maxillofac Surg
Pays: United States
ID NLM: 8206428

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 24 04 2018
revised: 28 10 2018
accepted: 25 11 2018
pubmed: 7 1 2019
medline: 26 6 2020
entrez: 7 1 2019
Statut: ppublish

Résumé

Apurinic/apyrimidinic endonuclease 1/redox factor-1 (APE1/Ref-1) is a multifunctional protein that shows elevated expression in many cancers, including oral squamous cell carcinoma (OSCC). However, the serum APE1/REF-1 level remains unknown in such patients. The purpose of the present study was to estimate the serum APE/Ref-1 levels in patients with OSCC and measure its association with the diagnosis, clinicopathologic features, and prognosis of OSCC. A total of 98 primary patients with OSCC and 109 age- or gender-matched normal controls were included in our case-control study. The predictor variable was the serum APE1/Ref-1 level, which was measured using an enzyme-linked immunosorbent assay. The outcome variables included diagnosis, clinicopathologic characteristics, treatment response, and OSCC prognosis. The optimal cutoff points of serum APE1/Ref-1 were identified using the X-tile program with minimum P values. Prognostic factors were evaluated using univariate and multivariate Cox regression models. The average patient and control age was 51.6 ± 8.7 years (63 men; 35 women) and 52.4 ± 10.3 years (67 men; 42 women), respectively. The serum APE1/Ref-1 level was significantly greater in patients with OSCC than that in the controls (4.56 ± 1.09 ng/mL vs 3.18 ± 0.88 ng/mL; P < .01). Much higher serum APE1/Ref-1 levels were observed in those with OSCC with late TNM stage, lymph node metastases, and worse pathologic differentiation. The receiver operating characteristic curve analysis illustrated that the serum APE1/Ref-1 level was a potential biomarker for differentiating OSCC, with an area under the curve of 0.83 (95% confidence interval, 0.78 to 0.88; sensitivity, 0.87; specificity, 0.68). The log-rank analysis revealed that patients with OSCC and a low APE1/Ref-1 level experienced longer disease-free survival after postoperative cisplatin chemotherapy and overall survival (P < .05). An elevated APE1/Ref-1 level might serve as a novel potential diagnostic biomarker for OSCC and can reflect the treatment response to cisplatin chemotherapy and prognosis.

Identifiants

pubmed: 30611690
pii: S0278-2391(18)31303-X
doi: 10.1016/j.joms.2018.11.034
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Endonucleases EC 3.1.-
APEX1 protein, human EC 4.2.99.18
DNA-(Apurinic or Apyrimidinic Site) Lyase EC 4.2.99.18
Cisplatin Q20Q21Q62J

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

859-866

Informations de copyright

Copyright © 2018 American Association of Oral and Maxillofacial Surgeons. Published by Elsevier Inc. All rights reserved.

Auteurs

Jianli Xie (J)

Attending Doctor, Department of Prosthodontics, Jinan Stomatological Hospital, Jinan, Shandong, People's Republic of China.

Ying Li (Y)

Nurse-in-Charge, Department of Liver Disease, Infectious Disease Hospital, Jinan, Shandong, People's Republic of China.

Jingjing Kong (J)

Resident, Department of Prosthodontics, Jinan Stomatological Hospital, Jinan, Shandong, People's Republic of China.

Chong Li (C)

Doctor, Department of Oral Medicine, Jinan Stomatological Hospital, Jinan, Shandong, People's Republic of China. Electronic address: jinandr_lc@163.com.

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Classifications MeSH