Associations between single-nucleotide polymorphisms of the VEGF gene and long-term prognosis of oral squamous cell carcinoma

被引:21
作者
Kaemmerer, P. W. [1 ,2 ,3 ]
Koch, F. P. [2 ]
Schiegnitz, E. [2 ]
Kumar, V. V. [2 ,3 ]
Berres, M. [4 ]
Toyoshima, T. [5 ]
Al-Nawas, B. [2 ]
Brieger, J. [6 ]
机构
[1] Harvard Univ, Sch Med, Boston, MA USA
[2] Univ Med Ctr, Dept Oral Maxillofacial & Plast Surg, D-55131 Mainz, Germany
[3] MR Ambedkar Dent Coll & Hosp, Bangalore, Karnataka, India
[4] Univ Med Ctr, IMBEI, D-55131 Mainz, Germany
[5] Kyushu Univ, Dept Oral & Maxillofacial Surg, Fukuoka 812, Japan
[6] Johannes Gutenberg Univ Mainz, Dept Otorhinolaryngol, D-55122 Mainz, Germany
关键词
advanced; long-term; oral squamous cell carcinoma; prognosis; single-nucleotide polymorphisms; smoking; VEGF; ENDOTHELIAL-GROWTH-FACTOR; ADVANCED BREAST-CANCER; FACTOR EXPRESSION; C/T POLYMORPHISM; RISK; SURVIVAL; BEVACIZUMAB; NICOTINE; PATHWAY; MARKERS;
D O I
10.1111/jop.12026
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction Functional polymorphisms (SNPs) of the vascular endothelial growth factor (VEGF) are associated with the incidence of oral squamous cell carcinoma (OSCC). An impact of VEGF-SNPs on prognosis of OSCC patients seems possible. Therefore, correlations between prognostic parameters of OSCC patients and five VEGF-SNPs were determined. Materials and Methods In a retrospective long-term study, in 113 OSCC patients that underwent curative resections, five VEGF-SNPs (1154G/A, +405G/C, +936 C/T, 2578 C/A, and 460 C/T) were analyzed. Associations between SNPs and prognosis (incidence of local recurrent disease, second cancer, metastases, death, total disease-free survival) were examined. Results After a mean follow-up time of 57.6months, 32 patients had local recurrences; 15 patients had second cancer, 15 patients metastases, and 23 patients died. The mean disease-free survival was 43.1months. A significant increased incidence of OSCC in smokers with the VEGF 2578 A/C and 460 C/T SNP was seen (each P<0.0001). In univariate analysis, patients with advanced OSCCs (T>2 or N>0) together with the 1154 A/A allele had a significant worse survival and a worse disease-free survival (both P<0.04). The same was seen for the +405G/G SNP (both P=0.002). In multivariate analysis, only the negative influence of the +405G/G SNP on survival in advanced OSCCs (T>2) could be confirmed (P=0.002). Discussion Possible reciprocal interactions between smoking and VEGF-SNP function were observed. Multivariate analysis confirmed the VEGF +405G/G genotype to be associated with poor survival in advanced OSCCs; a further use of this haplotype as biomarker has to be discussed.
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收藏
页码:374 / 381
页数:8
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