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长链非编码RNA、微小RNA和环状RNA在卵巢癌转移中的作用:途径与治疗方法

Long Non-Coding, Micro, and Circular RNAs in Ovarian Cancer Metastasis: Pathways and Treatment Approaches.

作者信息

Gosia Meeral, Doshi Gaurav, Parab Siddhi, Godad Angel

机构信息

Department of Pharmacology, SVKM's Dr. Bhanuben Nanavati College of Pharmacy, V L M Road, Vile Parle, Mumbai, 400056, India.

出版信息

Reprod Sci. 2025 Aug 15. doi: 10.1007/s43032-025-01948-x.

DOI:10.1007/s43032-025-01948-x
PMID:40815436
Abstract

Gynaecologic cancer is a major cause of death for women and the most well-known ovarian cancer (OC) has a high mortality rate. Given that the majority of ovarian cancer deaths are caused by metastatic tumors that have spread to nearby tissues, several biological processes, including angiogenesis and metastasis, have a role in the onset and course of these diseases. Numerous non-coding RNAs (ncRNAs) have been shown in recent studies to contribute to the invasion and metastasis of ovarian cancer by altering particular cellular pathways. Three forms of ncRNAs which are long non-coding RNAs, micro RNAs, and circular RNAs are the subjects of this review. miRNA is used as a potential biomarker such as miR-375 which is a serum exosome and also in therapeutics. lncRNA sponges with miRNA which sequesters and regulates tumor progression such as XIST miR-149-3p. circRNA targets proteins and regulates gene expression. This review provides an overview of the precise function of non-coding RNAs in the many pathways and molecular exchanges that contribute to the invasion and metastasis of malignancies. To increase the survival rate of OC patients, new approaches to ncRNA-targeted therapy are being utilised, including targeting lncRNAs and circRNAs and modulating the tumor microenvironment using exosomes.

摘要

妇科癌症是女性死亡的主要原因,最广为人知的卵巢癌(OC)死亡率很高。鉴于大多数卵巢癌死亡是由扩散到附近组织的转移性肿瘤引起的,包括血管生成和转移在内的几种生物学过程在这些疾病的发生和发展过程中发挥作用。最近的研究表明,许多非编码RNA(ncRNAs)通过改变特定的细胞途径促进卵巢癌的侵袭和转移。本文综述的三种ncRNAs形式为长链非编码RNA、微小RNA和环状RNA。miRNA被用作潜在的生物标志物,如血清外泌体中的miR-375,也用于治疗。lncRNA与miRNA结合,隔离并调节肿瘤进展,如XIST与miR-149-3p。circRNA靶向蛋白质并调节基因表达。本文综述了非编码RNA在导致恶性肿瘤侵袭和转移的多种途径和分子交换中的精确功能。为了提高OC患者的生存率,正在采用新的ncRNA靶向治疗方法,包括靶向lncRNAs和circRNAs以及使用外泌体调节肿瘤微环境。

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本文引用的文献

1
The up-regulation of PAK2 indicates unfavorable prognosis in patients with serous epithelial ovarian cancer and contributes to paclitaxel resistance in ovarian cancer cells.PAK2 的上调表明浆液性上皮性卵巢癌患者预后不良,并导致卵巢癌细胞对紫杉醇耐药。
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Targeting Ovarian Cancer Stem Cells by Dual Inhibition of the Long Noncoding RNA HOTAIR and Lysine Methyltransferase EZH2.靶向长链非编码 RNA HOTAIR 和赖氨酸甲基转移酶 EZH2 的双重抑制治疗卵巢癌干细胞。
Mol Cancer Ther. 2024 Nov 4;23(11):1666-1679. doi: 10.1158/1535-7163.MCT-23-0314.
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Drug resistance in ovarian cancer: from mechanism to clinical trial.
卵巢癌的耐药性:从机制到临床试验。
Mol Cancer. 2024 Mar 28;23(1):66. doi: 10.1186/s12943-024-01967-3.
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Identification of serum miR-1246 and miR-150-5p as novel diagnostic biomarkers for high-grade serous ovarian cancer.鉴定血清 miR-1246 和 miR-150-5p 作为高级别浆液性卵巢癌的新型诊断生物标志物。
Sci Rep. 2023 Nov 7;13(1):19287. doi: 10.1038/s41598-023-45317-7.
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Expression of circ-PHC3 enhances ovarian cancer progression via regulation of the miR-497-5p/SOX9 pathway.circ-PHC3 通过调控 miR-497-5p/SOX9 通路促进卵巢癌细胞的进展。
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Executive Summary of the Ovarian Cancer Evidence Review Conference.卵巢癌证据审查会议执行摘要。
Obstet Gynecol. 2023 Jul 1;142(1):179-195. doi: 10.1097/AOG.0000000000005211. Epub 2023 Jun 7.
7
Hsa_circ_0001741 Suppresses Ovarian Cancer Cell Proliferations Through Adsorption of miR-188-5p and Promotion of FOXN2 Expression.Hsa_circ_0001741 通过吸附 miR-188-5p 和促进 FOXN2 表达来抑制卵巢癌细胞增殖。
Mol Biotechnol. 2024 Jun;66(6):1477-1483. doi: 10.1007/s12033-023-00773-4. Epub 2023 Jun 15.
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Crosstalk between Genes and Long Non-Coding RNAs in Glioblastoma.胶质母细胞瘤中基因与长非编码 RNA 的相互作用。
Int J Mol Sci. 2023 Mar 28;24(7):6392. doi: 10.3390/ijms24076392.
9
HOTAIR: a potential metastatic, drug-resistant and prognostic regulator of breast cancer.HOTAIR:一种潜在的转移性、耐药性和乳腺癌预后调节因子。
Mol Cancer. 2023 Mar 30;22(1):65. doi: 10.1186/s12943-023-01765-3.
10
Exosome-transmitted circ Modulates Ovarian Cancer Metastasis via miR-378/ST5 Axis.外泌体传递的 circ 通过 miR-378/ST5 轴调节卵巢癌转移。
Mol Cell Biol. 2023 Jan;43(1):22-42. doi: 10.1080/10985549.2022.2160605. Epub 2023 Jan 26.