评估tp53信号通路基因核苷酸多态性在子宫不孕症因素诊断中的重要性

A. O. Putilo, T. A. Dzhibladze, N. Pozdnyakova, Nataliya Yu. Grygortsevich, E. Svidinskaya, V. Zuev, I. Khokhlova
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摘要

导读:世界卫生组织报告女性不孕症的发生率为30%,并且没有下降的趋势。同时,子宫因子在不孕症结构中占有重要地位,达50%。辅助生殖技术方法的改进可以成功地克服许多导致不孕症的原因,但该方法的可能性在子宫因素中受到限制。目的:评估TP53信号通路基因(LIF rs41281637, c.256GA;生物力学学报(自然科学版);MDM2 rs2279744, c.14+309TG;MDM4 rs1563828, c.558+572AG;TP53 rs1042522, c.215CG)在原发性和继发性不孕症患者子宫内膜中的表达。材料和方法:在2018 - 2021年,V.F. Snegirev妇产科诊所检查和治疗了54例26至48岁的原发性或继发性不孕症患者,包括子宫内膜遗传样本检查。第一组包括28例26至42岁的原发性不孕症患者。第二组患者26例,年龄29 ~ 48岁,继发性不孕症。结果:本研究评估了原发性和继发性不孕症患者TP53信号通路基因的核苷酸多态性表达。研究结果显示,在原发性和继发性不孕症患者中,核苷酸多态性LIF、MDM2、MDM4和TP53存在不同的变异,以及两组患者中LIF rs41281637 (G/ a)标记的同一性。结论:实验数据表明,TP53、LIF和MDM4信号通路基因的遗传多态性在女性原发性和MDM2继发性不孕症的发生中发挥了重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The importance of assessing nucleotide polymorphisms of the tp53 signaling pathway genes in uterine infertility factor diagnosis
INTRODUCTION: The WHO reported a 30% frequency of female infertility, which does not tend to decrease. Concurrently, the uterine factor occupies one of the most important places in infertility structure, reaching 50%. Improvement of assisted reproductive technology methods can successfully overcome many causes of infertility, but the possibilities of the method are limited in the uterine factor of infertility. AIM: To assess the presence of nucleotide polymorphisms of the TP53 signaling pathway genes (LIF rs41281637, c.256GA; LIF rs929271, n.397-2854TG; MDM2 rs2279744, c.14+309TG; MDM4 rs1563828, c.558+572AG; TP53 rs1042522, c.215CG) in the endometrium in patients with primary and secondary infertility. MATERIALS AND METHODS: In 20182021, the V.F. Snegirev Clinic of Obstetrics and Gynecology examined and treated 54 patients aged 26 to 48 years with primary or secondary infertility, including a genetic endometrial sample examination. The first group consisted of 28 patients with primary infertility aged 26 to 42 years. The 2nd group included 26 patients aged 29 to 48 years with secondary infertility. RESULTS: The study evaluated the expression of nucleotide polymorphisms of the TP53 signaling pathway genes in patients with primary and secondary infertility. Study results, data were obtained indicating various variants of nucleotide polymorphisms LIF, MDM2, MDM4, and TP53 in primary and secondary infertility, as well as the identity of a marker, such as LIF rs41281637 (G/A) in patients of both groups. CONCLUSION: The experimental data obtained indicate an important contribution of genetic polymorphisms in the genes of the TP53, LIF and MDM4 signaling pathway to the development of primary and MDM2 secondary infertility in women.
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