Shih Liang-Chun, Li Ching-Hao, Sun Kuo-Ting, Chen Liang-Yu, Hsu Che-Lun, Hung Yi-Wen, Wu Cheng-Nan, Hsia Te-Chun, Shen Te-Chun, Chang Wen-Shin, Shih Tzu-Ching, Tsai Chia-Wen, Bau DA-Tian
Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.
Department of Otolaryngology, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Anticancer Res. 2018 Apr;38(4):2087-2092. doi: 10.21873/anticanres.12448.
BACKGROUND/AIM: Matrix metalloproteinases (MMPs) play a critical role in inflammation and carcinogenesis, and the expression of mRNA MMP7 in oral squamous cell carcinoma tissues was higher than in the oral lichen planus or normal oral mucosa. However, the genotypic role of MMP7 has never been examined in oral cancer. Therefore, in the current study we aimed to examine the contribution of genotypic variants in the promoter region of MMP7 (A-181G and C-153T) to oral cancer risk in Taiwan.
In this hospital-based case-control study, 788 patients with oral cancer and 956 gender-and age-matched healthy controls were genotyped for MMP7 A-181G and C-153T via polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methodology.
The distribution pattern of AA, AG and GG for MMP7 promoter A-181G genotype was 88.2, 10.4 and 1.4% in the oral cancer patient group and 89.0, 9.3 and 1.7% in the healthy control group, respectively (p for trend=0.6779), non-significantly differentially distributed between the two groups. There is no polymorphic genotype for MMP7 C-153T among Taiwanese. The comparisons in allelic frequency distribution also support the findings that G allele may not be the risk determinant allele for oral cancer. There is no interaction between the genotypes of MMP7 with age, gender, smoking, alcohol or betel quid consumption on oral cancer risk.
Our results indicate that the MMP7 promoter genotypes only play an indirect role in determining the personal susceptibility to oral cancer in Taiwan.
背景/目的:基质金属蛋白酶(MMPs)在炎症和致癌过程中起关键作用,且口腔鳞状细胞癌组织中MMP7的mRNA表达高于口腔扁平苔藓或正常口腔黏膜。然而,MMP7的基因型作用在口腔癌中从未被研究过。因此,在本研究中,我们旨在探讨台湾地区MMP7启动子区域(A-181G和C-153T)的基因型变异对口腔癌风险的影响。
在这项基于医院的病例对照研究中,通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对788例口腔癌患者和956例年龄和性别匹配的健康对照进行MMP7 A-181G和C-153T基因分型。
口腔癌患者组中MMP7启动子A-181G基因型的AA、AG和GG分布模式分别为88.2%、10.4%和1.4%,健康对照组分别为89.0%、9.3%和1.7%(趋势p值=0.6779),两组间分布无显著差异。台湾人群中MMP7 C-153T无多态基因型。等位基因频率分布的比较也支持G等位基因可能不是口腔癌风险决定等位基因的发现。MMP7基因型与年龄、性别、吸烟、饮酒或嚼槟榔在口腔癌风险上无相互作用。
我们的结果表明,MMP7启动子基因型在决定台湾地区个体对口腔癌的易感性方面仅起间接作用。