平滑肌瘤患者与健康人群雌激素受体-α基因(T/C)多态性的比较

H. Hoseini, A. Sarani, Afsaneh Sarabandi, Masoud Kerman Saravi
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引用次数: 0

摘要

背景:平滑肌瘤是女性最常见的肿瘤之一,多发于育龄期,其病因尚不清楚。激素疗法是治疗这种疾病的常用方法之一。雌激素通过受体ER α在平滑肌瘤的治疗中发挥有效作用。单核苷酸多态性(snp)在许多疾病和肿瘤的诊断、治疗和预后中都是有效的。为此,本研究调查了锡斯坦和俾路支斯坦省、扎黑丹省平滑肌瘤妇女雌激素受体ER α基因多态性,并与健康人群进行了比较。材料和方法:总共选取了150名患有平滑肌瘤的妇女,并分离了她们的DNA。另外,从健康个体中抽取150个样本作为对照组。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法和pvii方法研究基因多态性。结果:ER α基因多态性与子宫肌瘤的发生有显著关系。结论:该基因多态性可作为扎黑丹、锡斯坦和俾路支斯坦省伊朗妇女平滑肌瘤预后的标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Estrogen Receptor-α Gene (T/C) Polymorphism in Patients With Leiomyoma Compared to Healthy Individuals
Background: Leiomyoma as one of the most prevalent tumors in women occurs at the same time of reproductive age and its causes are still unknown. Hormone therapy is one of the common treatments for this disease. Estrogen hormone through its receptor, which is called ER α, plays an effective role in the treatment of leiomyoma. Single nucleotide polymorphisms (SNPs) are effective in the diagnosis, treatment, and prognosis of many diseases and tumors. In this regard, the current study investigated the estrogen receptor gene polymorphisms of ER α in women with leiomyoma in Sistan and Baluchestan province, Zahedan and then compared them with healthy individuals. Materials and Methods: Overall, 150 women with leiomyoma were sampled and their DNA was isolated as well. In addition, 150 samples were taken from healthy individuals as the control group. The polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and PvuII were used to study gene polymorphisms. Results: The results showed a significant relationship between ER α gene polymorphism and leiomyoma. Conclusion: Accordingly, this gene polymorphism can be considered as a marker for prognosis in leiomyoma in the population of Iranian women in Zahedan, Sistan and Baluchestan province.
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