Hu Rei-Hsing, Chuang Chun-Yi, Lin Chiao-Wen, Su Shih-Chi, Chang Lun-Ching, Wu Ssu-Wei, Liu Yu-Fan, Yang Shun-Fa
Department of Biomedical Sciences, Chung Shan Medical University, Taichung 402, Taiwan.
School of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
J Pers Med. 2021 May 31;11(6):490. doi: 10.3390/jpm11060490.
MACC1 (Metastasis Associated in Colon Cancer 1) is found to regulate the hepatocyte growth factor (HGF)/Met signal pathway, and plays an important role in tumor proliferation, angiogenesis, and metastasis. However, the relationships between SNPs (single nucleotide polymorphisms) and oral cancer are still blurred. In this study, five SNPs (rs3095007, rs1990172, rs4721888, rs975263, and rs3735615) were genotyped in 911 oral cancer patients and 1200 healthy individuals by real-time polymerase chain reaction (PCR), and the associations of oral cancer with the SNP genotypes, environmental risk factors, and clinicopathological characteristics were further analyzed. Our results showed that individuals who had GC genotype or C-allele (GC + CC) in rs4721888 would have a higher risk for oral cancer incidence than GG genotype after adjustment for betel quid chewing, cigarette smoking, and alcohol drinking. Moreover, the 715 oral cancer patients with a betel quid chewing habit, who had C-allele (TC + CC) in rs975263, would have a higher risk for lymph node metastasis. Further analyses of the sequences of rs4721888 revealed that the C-allele of rs4721888 would be a putative exonic splicing enhancer. In conclusion, SNP rs4721888 would elevate the susceptibility for oral cancer, and SNP rs975263 would increase the metastasis risk for oral cancer patients with a betel quid chewing habit. Our data suggest that SNP rs4721888 could be a putative genetic marker for oral cancer, and SNP rs975362 may have the potential to be a prognostic marker of metastasis in an oral cancer patient.
结肠癌转移相关蛋白1(MACC1)被发现可调控肝细胞生长因子(HGF)/Met信号通路,并在肿瘤增殖、血管生成和转移中发挥重要作用。然而,单核苷酸多态性(SNP)与口腔癌之间的关系仍不明确。在本研究中,通过实时聚合酶链反应(PCR)对911例口腔癌患者和1200名健康个体的5个SNP(rs3095007、rs1990172、rs4721888、rs975263和rs3735615)进行基因分型,并进一步分析口腔癌与SNP基因型、环境危险因素及临床病理特征之间的关联。我们的结果显示,在校正嚼槟榔、吸烟和饮酒因素后,rs4721888中具有GC基因型或C等位基因(GC + CC)的个体患口腔癌的风险高于GG基因型个体。此外,715例有嚼槟榔习惯的口腔癌患者中,rs975263中具有C等位基因(TC + CC)的患者发生淋巴结转移的风险更高。对rs4721888序列的进一步分析表明,rs4721888的C等位基因可能是一个外显子剪接增强子。总之,SNP rs4721888会增加患口腔癌的易感性,SNP rs975263会增加有嚼槟榔习惯的口腔癌患者的转移风险。我们的数据表明,SNP rs4721888可能是口腔癌的一个潜在遗传标志物,SNP rs975362可能有潜力成为口腔癌患者转移的预后标志物。