Zhang Siyi, Liu Shanshan, Chen Wenchu, Yan Yaping, Cai Mansi, Liu Xiaoping, Luo Ailing, Li Wenjuan, Yi Lisha, Xu Yingyi
Department of Anesthesiology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangdong Provincial Clinical Research Center for Child Health, Guangzhou, 510623, China.
Department of Hematology and Oncology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangdong Provincial Clinical Research Center for Child Health, Guangzhou, 510623, China.
J Cancer. 2024 Feb 4;15(6):1762-1769. doi: 10.7150/jca.90379. eCollection 2024.
: The potential relation of methyltransferase-like gene polymorphisms and epithelial ovarian cancer (EOC) remains unclear. Five SNPs ( rs3769767 A>G, rs1056321 T>C, rs10190853 G>A, rs3769768 G>A and rs11869256 A>G) of methyltransferase-like genes was selected trough NCBI dbSNP database. Two hundred and eighty-eight cases and 361 controls were enrolled from three hospitals in South China to conduct the case-control study. Genomic DNA was abstracted from peripheral blood and genotyped through a TapMan assay. Stratified analysis was conducted to explore the association of rs10190853, rs3769768, rs11869256 genotype and EOC susceptibility. The combination analysis was adopted to evaluate the relation between inferred haplotypes of the genes and EOC risk. Multifactor dimensionality reduction (MDR) analysis was performed to verify the interaction of SNPs. Among the five analyzed SNPs, rs3769768 AA exhibited a significant association with increased EOC risk, while rs10190853 GA, rs11869256 GA was certified to decrease the susceptibility of EOC. The stratified analysis further revealed the harmful effect of rs3769768 AA in EOC patients. On the contrary, rs11869256 AG/GG and rs10190853 AA showed the reduced risk of EOC in patients of specific subgroups. Combination analysis identified that haplotypes AAA highly connected with reduced risk of EOC. MDR analysis revealed that these SNPs existed no specific interactions. : rs3769768 was related to increased risk of EOC. rs10190853 and rs11869256 decreased the susceptibility in EOC. and could be potential target of molecular therapy and prognosis markers.
甲基转移酶样基因多态性与上皮性卵巢癌(EOC)之间的潜在关系仍不清楚。通过NCBI dbSNP数据库选择了甲基转移酶样基因的5个单核苷酸多态性(SNPs)(rs3769767 A>G、rs1056321 T>C、rs10190853 G>A、rs3769768 G>A和rs11869256 A>G)。从中国南方的三家医院招募了288例病例和361例对照进行病例对照研究。从外周血中提取基因组DNA,并通过TaqMan分析进行基因分型。进行分层分析以探讨rs10190853、rs3769768、rs11869256基因型与EOC易感性的关联。采用组合分析来评估这些基因的推断单倍型与EOC风险之间的关系。进行多因素降维(MDR)分析以验证SNPs之间的相互作用。在分析的5个SNPs中,rs3769768 AA与EOC风险增加显著相关,而rs10190853 GA、rs11869256 GA被证实可降低EOC的易感性。分层分析进一步揭示了rs3769768 AA对EOC患者的有害影响。相反,rs11869256 AG/GG和rs10190853 AA在特定亚组患者中显示出EOC风险降低。组合分析确定单倍型AAA与EOC风险降低高度相关。MDR分析表明这些SNPs不存在特定相互作用。rs3769768与EOC风险增加有关。rs10190853和rs11869256降低了EOC的易感性,并且可能是分子治疗的潜在靶点和预后标志物