微rna在卵巢功能不全中的作用及意义。

IF 1.5 4区 医学 Q4 GENETICS & HEREDITY
Hui Gao, Xi-Xia Cao, Hua Hua, Hui Zhu
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引用次数: 0

摘要

背景:卵巢功能不全(POI)是女性在40岁之前卵巢功能过早下降的一种疾病,表现为月经不规律,如闭经或少经,卵泡刺激素水平升高超过25 U/L,雌激素水平逐渐下降。尽管进行了大量研究,但POI的确切致病机制仍不清楚。本研究的重点是microRNAs (miRNAs)在POI发展中的作用。作为基因表达的关键调控因子,mirna可能在POI的诊断和创新治疗方法的开发中发挥重要作用。方法:在PubMed上进行全面的文献检索。我们纳入了截至2024年9月用英语发表的研究。我们的搜索使用了以下关键词的组合:microRNA,卵巢早衰(POI)和卵巢早衰(POF)。文章通过标题过滤,然后通过全文审查,只选择那些与我们感兴趣的主题及其相关领域相关的文章。结果:mirna已成为POI的关键调节因子,介导一系列促进疾病进展的生物学过程。它们的参与为早期诊断、预后评估和治疗干预提供了有希望的见解,突出了它们作为生物标志物和治疗靶点的潜力。结论:阐明mirna在POI中的作用为治疗该疾病开辟了新的途径。通过了解mirna如何影响POI的分子机制,可以开发诊断和治疗的创新策略,从而潜在地改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Functions and Implications of MicroRNAs in Premature Ovarian Insufficiency.

Background: Premature ovarian insufficiency (POI) is a condition in women characterized by the premature decline of ovarian function before age 40, evident through menstrual irregularities such as amenorrhea or oligomenorrhea, elevated FSH levels exceeding 25 U/L, and a progressive decrease in estrogen levels. Despite considerable research, the exact pathogenic mechanisms underlying POI remain unclear. This study focuses on the role of microRNAs (miRNAs) in the development of POI. As critical regulators of gene expression, miRNAs may play significant roles in diagnosis and the development of innovative therapeutic approaches for POI.

Methods: A comprehensive literature search was conducted on PubMed for this review. We included studies published in English up to September 2024. Our search utilized a combination of the following keywords: microRNA, premature ovarian insufficiency (POI), and premature ovarian failure (POF). Articles were filtered by title and subsequently through full-text review, selecting only those pertinent to our topics of interest and their related areas.

Results: miRNAs have emerged as critical regulators in POI, mediating a range of biological processes that contribute to the disease's progression. Their involvement offers promising insights for early diagnosis, prognostic assessments, and therapeutic interventions, highlighting their potential as biomarkers and therapeutic targets.

Conclusion: Elucidating miRNAs' roles in POI opens new avenues for managing the disease. By understanding how miRNAs influence the molecular mechanisms of POI, innovative strategies can be developed for diagnosis and treatment, potentially improving patient outcomes.

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来源期刊
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
4.20
自引率
0.00%
发文量
241
审稿时长
14 weeks
期刊介绍: Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care. Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.
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