Laboratório de Imunopatologia Keizo Asami, Universidade Federal de Pernambuco, Av. Prof. Moraes Rego, S/N, Recife, 50670-901, Brazil.
Departamento de Bioquímica, Universidade Federal de Pernambuco, Av. Prof. Moraes Rego, S/N, Recife, 50670-901, Brazil.
Mol Biol Rep. 2019 Jun;46(3):3531-3536. doi: 10.1007/s11033-019-04780-0. Epub 2019 Mar 30.
FUT3 gene is responsible for encode an homonymous α1,3/4-fucosyltransferase involved in the synthesis of sialyl-Lewis antigens. FUT3-fucosylated glycoconjugates play key roles in pathways involved in tumor biology and metastasis, such as cellular ligation to E-selectins, TGF-β-induced epithelial-mesenchymal transition, NK cell-mediated tumor cytotoxicity and apoptosis. Tumor-associated FUT3 promoter polymorphism rs2306969 (-6951 C> T, position related to the gene's translation start site) has been linked to breast, ovarian and intestinal gastric cancer. Although non-coding polymorphisms accounts for the majority of variations founded in breast cancer, their functional roles are still poorly understood. This study aimed to investigate the impact of different alleles for this variation in FUT3 expression of invasive breast tumors. A luciferase reporter assay was performed using two breast tumor cell lines to evaluate respectively the impact of FUT3 rs2306969 (-6951 CC) and (-6951 TT) on protein expression. Gene and protein expressions were also measured in twenty-nine fresh biopsies of invasive breast tumors. Rs2306969 did not significantly influence FUT3 expression in both used systems. However, this study is defiant since the biological role of this polymorphism in breast cancer and other tumor types could be linked to cis/trans modulation of other genes, respond to different environmental stimuli or impact gene expression only in association with other variations. Rs2306969 did not modulate FUT3 expression in breast tumors under non-stimulated conditions. Nevertheless, our study contributes to the notably challenging task that is to understand how non-coding polymorphisms can drive the overall risk in cancer development.
FUT3 基因负责编码一种同型的α1,3/4-岩藻糖基转移酶,参与唾液酸化-Lewis 抗原的合成。FUT3 岩藻糖化糖缀合物在肿瘤生物学和转移途径中发挥关键作用,例如细胞与 E-选择素的连接、TGF-β诱导的上皮-间充质转化、NK 细胞介导的肿瘤细胞毒性和细胞凋亡。肿瘤相关的 FUT3 启动子多态性 rs2306969(-6951 C>T,与基因翻译起始位点相关的位置)与乳腺癌、卵巢癌和胃肠道癌有关。尽管非编码多态性占乳腺癌中发现的大多数变异,但它们的功能作用仍知之甚少。本研究旨在研究 FUT3 表达中这种变异的不同等位基因对浸润性乳腺癌的影响。使用两种乳腺癌细胞系进行荧光素酶报告基因检测,分别评估 FUT3 rs2306969(-6951 CC)和(-6951 TT)对蛋白表达的影响。还在 29 份浸润性乳腺癌新鲜活检标本中测量了基因和蛋白表达。rs2306969 在用的两种系统中均未显著影响 FUT3 表达。然而,由于该多态性在乳腺癌和其他肿瘤类型中的生物学作用可能与其他基因的顺式/反式调节、对不同环境刺激的反应或仅在与其他变异相关时影响基因表达有关,因此该研究存在争议。rs2306969 在非刺激条件下不调节乳腺癌中的 FUT3 表达。然而,我们的研究有助于理解非编码多态性如何能导致癌症发展的总体风险,这是一个极具挑战性的任务。