Glatthaar Hanna, Katto Judith, Vogt Thomas, Mahlknecht Ulrich
Trauma and Hand Surgery, St. Vincentius Hospital Karlsruhe, Germany.
Biologist, José Carreras Center for Immuno and Gene Therapy, University of Saarland, Homburg/Saar, Germany.
Genet Epigenet. 2016 Feb 24;8:1-6. doi: 10.4137/GEG.S31264. eCollection 2016.
The incidence of malignant melanoma in the developed world is continuously increasing. We conducted a case-control study in order to evaluate the association between each of the four estrogen receptor alpha polymorphisms (ESR1 single-nucleotide polymorphisms [SNPs] +2464C/T, -4576A/C, +1619A/G, and +6362C/T) and malignant melanoma susceptibility and disease course. The study population consisted of 205 Caucasian patients who were diagnosed as having malignant melanoma and 208 healthy Caucasian controls. Through DNA genotyping, we identified a SNP-dependent malignant melanoma susceptibility as well as a SNP-dependent effect on the course of disease and response to therapy.
在发达国家,恶性黑色素瘤的发病率持续上升。我们开展了一项病例对照研究,以评估雌激素受体α的四种多态性(ESR1单核苷酸多态性[SNPs]+2464C/T、-4576A/C、+1619A/G和+6362C/T)中的每一种与恶性黑色素瘤易感性及疾病进程之间的关联。研究人群包括205名被诊断患有恶性黑色素瘤的白种人患者和208名健康的白种人对照。通过DNA基因分型,我们确定了一种单核苷酸多态性依赖性的恶性黑色素瘤易感性,以及对疾病进程和治疗反应的单核苷酸多态性依赖性影响。