Elevated plasma level of visfatin/pre-b cell colony-enhancing factor in male oral squamous cell carcinoma patients

被引:26
作者
Tsai Yu-Duan [1 ]
Wang Chao-Ping [2 ]
Chen Chih-Yu [4 ]
Lin Li-Wen [4 ]
Lin Tsun-Mei [5 ,6 ]
Hsu Chia-Chang [3 ]
Chung Fu-Mei [2 ]
Lin Hsien-Chang [7 ]
Hsu Hsia-Fen [8 ]
Lee Yau-Jiunn [9 ]
Houng Jer-Yiing [8 ]
机构
[1] I Shou Univ, E Da Hosp, Dept Surg, Div Neurol, Kaohsiung 82445, Taiwan
[2] I Shou Univ, E Da Hosp, Div Cardiol, Kaohsiung 82445, Taiwan
[3] I Shou Univ, E Da Hosp, Dept Internal Med, Div Gastroenterol & Hepatol, Kaohsiung 82445, Taiwan
[4] I Shou Univ, E Da Hosp, Dept Dent, Kaohsiung 82445, Taiwan
[5] I Shou Univ, E Da Hosp, Dept Lab Med, Kaohsiung 82445, Taiwan
[6] I Shou Univ, E Da Hosp, Dept Med Res, Kaohsiung 82445, Taiwan
[7] INC Kaohsiung, Li Tzung Biotechnol, Kaohsiung 80143, Taiwan
[8] I Shou Univ, Dept Med Nutr, Inst Biotechnol & Chem Engn, Kaohsiung 82445, Taiwan
[9] Lees Endocrinol Clin Pingtung, Pingtung 90000, Taiwan
来源
MEDICINA ORAL PATOLOGIA ORAL Y CIRUGIA BUCAL | 2013年 / 18卷 / 02期
关键词
Visfatin; oral squamous cell carcinomas; white blood cell count; neutrophil count; CAVITY CANCER-RISK; NICOTINAMIDE PHOSPHORIBOSYLTRANSFERASE; INFLAMMATION; ADIPOCYTOKINE; RESISTIN; MARKERS; LEPTIN; INDIA;
D O I
10.4317/medoral.18574
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: Visfatin, also known as nicotiamide phosphoribosyltransferase or pre-B cell colony enhancing factor, is a pro-inflammatory cytokine whose serum level is increased in various cancers. In this study, we investigated whether plasma visfatin levels were altered in patients with oral squamous cell carcinoma (OSCC). The relationship between plasma visfatin levels and the pretreatment hematologic profile was also explored. Study Design: Plasma visfatin concentrations were measured through ELISA in OSCC patients and control subjects. A total of 51 patients with OSCC and 57 age-and body mass index (BMI)-matched control subjects were studied. All study subjects were male. Results: Plasma visfatin was found to be elevated in patients with OSCC (7.0 +/- 4.5 vs. 4.8 +/- 1.9 ng/ml, p = 0.002). Multiple logistic regression analysis revealed visfatin as an independent association factor for OSCC, even after full adjustment of known biomarkers. Visfatin level was significantly correlated with white blood cell (WBC) count, neutrophil count, and hematocrit (all p < 0.05). In addition, WBC count, neutrophil count, and visfatin gradually increased with stage progression, and hematocrit gradually decreased with stage progression (all p < 0.05). Conclusion: Increased plasma visfatin levels were associated with OSCC, independent of risk factors, and were correlated with inflammatory biomarkers. These data suggest that visfatin may act through inflammatory reactions to play an important role in the pathogenesis of OSCC.
引用
收藏
页码:E180 / E186
页数:7
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