Centro de Investigación Genética y Genómica, Facultad de Ciencias de la Salud Eugenio Espejo, Universidad Tecnológica Equinoccial, Avenue Mariscal Sucre, 170129 Quito, Ecuador.
Gene Regulation, Stem Cells and Cancer Programme, Centre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Universitat Pompeu Fabra (UPF), Dr. Aiguader 88 Street, 08003 Barcelona, Spain.
Biomed Res Int. 2017;2017:3507671. doi: 10.1155/2017/3507671. Epub 2017 Jun 8.
Prostate cancer (PC) is the second most commonly diagnosed type of cancer in males with 1,114,072 new cases in 2015. The MTHFR enzyme acts in the folate metabolism, which is essential in methylation and synthesis of nucleic acids. MTHFR C677T alters homocysteine levels and folate assimilation associated with DNA damage. Androgens play essential roles in prostate growth. The SRD5A2 enzyme metabolizes testosterone and the V89L polymorphism reduces in vivo SRD5A2 activity. The androgen receptor gene codes for a three-domain protein that contains two polymorphic trinucleotide repeats (CAG, GGC). Therefore, it is essential to know how PC risk is associated with clinical features and polymorphisms in high altitude Ecuadorian mestizo populations. We analyzed 480 healthy and 326 affected men from our three retrospective case-control studies. We found significant association between MTHFR C/T (odds ratio [OR] = 2.2; = 0.009), MTHFR C/T+T/T (OR = 2.22; = 0.009), and PC. The SRD5A2 A49T substitution was associated with higher pTNM stage (OR = 2.88; = 0.039) and elevated Gleason grade (OR = 3.15; = 0.004). Additionally, patients with ≤21 CAG repeats have an increased risk of developing PC (OR = 2.99; < 0.001). In conclusion, genotype polymorphism studies are important to characterize genetic variations in high altitude mestizo populations.
前列腺癌(PC)是男性中第二大常见的癌症类型,2015 年新发病例为 1,114,072 例。MTHFR 酶参与叶酸代谢,这对于甲基化和核酸合成至关重要。MTHFR C677T 改变同型半胱氨酸水平和叶酸摄取,与 DNA 损伤有关。雄激素在前列腺生长中发挥重要作用。SRD5A2 酶代谢睾酮,V89L 多态性降低体内 SRD5A2 活性。雄激素受体基因编码一个包含两个多态三核苷酸重复(CAG、GGC)的三域蛋白。因此,了解 PC 风险与临床特征和高海拔厄瓜多尔混血人群中的多态性之间的关系至关重要。我们分析了来自我们三项回顾性病例对照研究的 480 名健康男性和 326 名患病男性。我们发现 MTHFR C/T(比值比[OR] = 2.2; = 0.009)、MTHFR C/T+T/T(OR = 2.22; = 0.009)与 PC 之间存在显著关联。SRD5A2 A49T 取代与更高的 pTNM 分期(OR = 2.88; = 0.039)和升高的 Gleason 分级(OR = 3.15; = 0.004)相关。此外,CAG 重复≤21 的患者发生 PC 的风险增加(OR = 2.99; < 0.001)。总之,基因型多态性研究对于描述高海拔混血人群中的遗传变异很重要。