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卵巢颗粒细胞中的长非编码 RNA。

Long non-coding RNAs in ovarian granulosa cells.

机构信息

Department of Gynecology, The First Affiliated Hospital of Shenzhen University, Health Science Center, Shenzhen Second People's Hospital, 3002 Sungang West Road, Futian District, Shenzhen, 518000, Guangdong province, China.

Key Laboratory of Anti-Inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-Inflammatory and Immune Medicine, Institute of Clinical Pharmacology, Anhui Medical University, 81 Meishan Road, Hefei, 230032, Anhui province, China.

出版信息

J Ovarian Res. 2020 Jun 5;13(1):63. doi: 10.1186/s13048-020-00663-2.

DOI:10.1186/s13048-020-00663-2
PMID:32503679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7275442/
Abstract

Granulosa cells (GCs) are somatic cells surrounding oocytes within follicles and are essential for folliculogenesis. Pathological changes in GCs are found in several ovarian disorders. Recent reports have indicated that long non-coding RNAs (lncRNAs), which modulate gene expression via multiple mechanisms, are key regulators of the normal development of GCs, follicles, and ovaries. In addition, accumulating evidence has suggested that lncRNAs can be utilized as biomarkers for the diagnosis and prognosis of GC-related diseases, such as polycystic ovary syndrome (PCOS) and premature ovarian insufficiency (POI). Therefore, lncRNAs not only play a role in GCs that are involved in normal folliculogenesis, but they may also be considered as potential candidate biomarkers and therapeutic targets in GCs under pathological conditions. In the future, a detailed investigation of the in vivo delivery or targeting of lncRNAs and large-cohort-validation of the clinical applicability of lncRNAs is required.

摘要

颗粒细胞(GCs)是围绕卵泡内卵母细胞的体细胞,对于卵泡发生至关重要。GCs 的病理变化存在于几种卵巢疾病中。最近的报告表明,长非编码 RNA(lncRNAs)通过多种机制调节基因表达,是 GCs、卵泡和卵巢正常发育的关键调节剂。此外,越来越多的证据表明,lncRNAs 可用作与 GC 相关疾病(如多囊卵巢综合征(PCOS)和卵巢早衰(POI))的诊断和预后的生物标志物。因此,lncRNAs 不仅在参与正常卵泡发生的 GCs 中发挥作用,而且在病理条件下的 GCs 中也可以被视为潜在的候选生物标志物和治疗靶点。未来需要对 lncRNAs 的体内递药或靶向进行详细研究,并对 lncRNAs 的临床适用性进行大样本队列验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4192/7275442/3fdc4c3004f9/13048_2020_663_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4192/7275442/50eb316b3aee/13048_2020_663_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4192/7275442/534a21224e0b/13048_2020_663_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4192/7275442/3fdc4c3004f9/13048_2020_663_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4192/7275442/50eb316b3aee/13048_2020_663_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4192/7275442/534a21224e0b/13048_2020_663_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4192/7275442/3fdc4c3004f9/13048_2020_663_Fig3_HTML.jpg

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Mol Ther Nucleic Acids. 2020 Jun 5;20:205-216. doi: 10.1016/j.omtn.2020.02.007. Epub 2020 Feb 13.
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Long noncoding RNA HCP5 participates in premature ovarian insufficiency by transcriptionally regulating MSH5 and DNA damage repair via YB1.长非编码 RNA HCP5 通过转录调控 MSH5 和 YB1 参与 DNA 损伤修复,从而导致卵巢早衰。
Nucleic Acids Res. 2020 May 7;48(8):4480-4491. doi: 10.1093/nar/gkaa127.
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LncPrep + 96kb inhibits ovarian fibrosis by upregulating prolyl oligopeptidase expression.
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Mol Med Rep. 2025 May;31(5). doi: 10.3892/mmr.2025.13478. Epub 2025 Feb 28.
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