• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

微小RNA介导的卵巢癌治疗方法:一项全面的系统综述。

MicroRNA‑mediated approaches in ovarian cancer therapy: A comprehensive systematic review.

作者信息

Putri Henny Meitri Andrie Rachmasari, Novianti Putri Wikie, Pradjatmo Heru, Haryana Sofia Mubarika

机构信息

Department of Obstetrics and Gynecology, Indonesia Army Hospital, Central Jakarta 10410, Indonesia.

Siena Clinical, Central Jakarta 10340, Indonesia.

出版信息

Oncol Lett. 2024 Aug 12;28(4):491. doi: 10.3892/ol.2024.14624. eCollection 2024 Oct.

DOI:10.3892/ol.2024.14624
PMID:39185494
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11342411/
Abstract

Ovarian cancer (OC) poses a significant health risk to women worldwide, with late diagnoses and chemotherapy resistance leading to high mortality rates. Despite several histological subtypes, the primary challenge remains the subtle nature of its symptoms, resulting in advanced-stage diagnosis and reduced treatment success rates. With platinum-based therapies showing relative efficacy but limited survival enhancements, the emergence of chemotherapy resistance during recurrence remains a critical obstacle. Precision medicine development has aimed to address these challenges in the context of the molecular diversity of OC. The present review explored the landscape of microRNA (miRNA)-mediated approaches in OC treatment. miRNAs have emerged as regulators of gene expression, serving as both oncogenes and tumor suppressors in OC. Dysregulated miRNAs are associated with disease progression and chemotherapy resistance, underscoring their significance in diagnosis and tailored treatment strategies. The present review extracted 295 publications from the PUBMED database. Out of the 73 eligible studies, 55 miRNAs were assessed. A total of three of these miRNAs were not associated with any disease or cancer, whilst eight were associated with OC, albeit also associated with other diseases. The present review encompassed three dimensions: i) The role of miRNAs in treatment efficacy; ii) the use of miRNAs to enhance therapy outcomes; and iii) adjunctive strategies for improved treatment results. Furthermore, it offered insights into potential avenues for improving OC treatment using miRNA-based approaches.

摘要

卵巢癌(OC)对全球女性的健康构成重大风险,晚期诊断和化疗耐药导致高死亡率。尽管存在几种组织学亚型,但主要挑战仍然是其症状的隐匿性,导致晚期诊断和治疗成功率降低。由于铂类疗法显示出相对疗效,但生存改善有限,复发期间化疗耐药的出现仍然是一个关键障碍。精准医学的发展旨在在OC分子多样性的背景下应对这些挑战。本综述探讨了微小RNA(miRNA)介导的方法在OC治疗中的前景。miRNA已成为基因表达的调节因子,在OC中既作为癌基因又作为肿瘤抑制因子。miRNA失调与疾病进展和化疗耐药相关,突显了它们在诊断和定制治疗策略中的重要性。本综述从PUBMED数据库中提取了295篇出版物。在73项符合条件的研究中,评估了55种miRNA。其中共有3种miRNA与任何疾病或癌症无关,而8种与OC相关,尽管也与其他疾病相关。本综述涵盖三个方面:i)miRNA在治疗疗效中的作用;ii)使用miRNA提高治疗效果;iii)改善治疗结果的辅助策略。此外,它还为使用基于miRNA的方法改善OC治疗的潜在途径提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/8d65d2693bbd/ol-28-04-14624-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/8968d8f78216/ol-28-04-14624-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/5466217158a0/ol-28-04-14624-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/885ad6c53b0f/ol-28-04-14624-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/8d65d2693bbd/ol-28-04-14624-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/8968d8f78216/ol-28-04-14624-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/5466217158a0/ol-28-04-14624-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/885ad6c53b0f/ol-28-04-14624-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a961/11342411/8d65d2693bbd/ol-28-04-14624-g03.jpg

相似文献

1
MicroRNA‑mediated approaches in ovarian cancer therapy: A comprehensive systematic review.微小RNA介导的卵巢癌治疗方法:一项全面的系统综述。
Oncol Lett. 2024 Aug 12;28(4):491. doi: 10.3892/ol.2024.14624. eCollection 2024 Oct.
2
MicroRNAs as the critical regulators of Cisplatin resistance in ovarian cancer cells.MicroRNAs 作为卵巢癌细胞顺铂耐药的关键调节因子。
J Ovarian Res. 2021 Sep 30;14(1):127. doi: 10.1186/s13048-021-00882-1.
3
The Role of miRNA in Ovarian Cancer: an Overview.miRNA 在卵巢癌中的作用:概述。
Reprod Sci. 2022 Oct;29(10):2760-2767. doi: 10.1007/s43032-021-00717-w. Epub 2022 Jan 1.
4
Double Insurance for OC: miRNA-Mediated Platinum Resistance and Immune Escape.双重保险应对 OC:miRNA 介导的铂耐药和免疫逃逸。
Front Immunol. 2021 Apr 1;12:641937. doi: 10.3389/fimmu.2021.641937. eCollection 2021.
5
Optimal chemotherapy treatment for women with recurrent ovarian cancer.复发性卵巢癌女性的最佳化疗治疗。
Curr Oncol. 2007 Oct;14(5):195-208. doi: 10.3747/co.2007.148.
6
A diagnostic miRNA panel to detect recurrence of ovarian cancer through artificial intelligence approaches.通过人工智能方法检测卵巢癌复发的诊断 miRNA 面板。
J Cancer Res Clin Oncol. 2023 Jan;149(1):325-341. doi: 10.1007/s00432-022-04468-2. Epub 2022 Nov 15.
7
Research Advances in the Roles of N6-Methyladenosine Modification in Ovarian Cancer.N6-甲基腺苷修饰在卵巢癌中作用的研究进展。
Cancer Control. 2024 Jan-Dec;31:10732748241256819. doi: 10.1177/10732748241256819.
8
Differential role of microRNAs in prognosis, diagnosis, and therapy of ovarian cancer.微小RNA在卵巢癌预后、诊断及治疗中的差异作用
Biomed Pharmacother. 2016 Dec;84:592-600. doi: 10.1016/j.biopha.2016.09.087. Epub 2016 Sep 30.
9
Transcriptomic analysis reveals tumor stage- or grade-dependent expression of miRNAs in serous ovarian cancer.转录组分析揭示了浆液性卵巢癌中 miRNA 与肿瘤分期或分级相关的表达。
Hum Cell. 2021 May;34(3):862-877. doi: 10.1007/s13577-021-00486-3. Epub 2021 Feb 12.
10
The prognostic role of microRNA in epithelial ovarian cancer: a systematic review of literature with an overall survival meta-analysis.微小RNA在上皮性卵巢癌中的预后作用:一项文献系统综述及总生存的Meta分析
Oncotarget. 2020 Mar 24;11(12):1085-1095. doi: 10.18632/oncotarget.27246.

引用本文的文献

1
Signaling networks and MiRNA crosstalk in ovarian cancer chemoresistance.卵巢癌化疗耐药中的信号网络与微小RNA相互作用
J Ovarian Res. 2025 Aug 14;18(1):185. doi: 10.1186/s13048-025-01770-8.
2
Exosomal miRNA-based theranostics in cervical cancer: bridging diagnostics and therapy.基于外泌体微小RNA的宫颈癌诊疗一体化:连接诊断与治疗
Med Oncol. 2025 May 4;42(6):193. doi: 10.1007/s12032-025-02752-y.

本文引用的文献

1
Prognostic factors and clinic-pathologic characteristics of ovarian tumor with different histologic subtypes-a SEER database population study of 41,376 cases.不同组织学亚型卵巢肿瘤的预后因素及临床病理特征——一项基于监测、流行病学和最终结果(SEER)数据库41376例病例的人群研究
Transl Cancer Res. 2023 Aug 31;12(8):1937-1950. doi: 10.21037/tcr-23-58. Epub 2023 Aug 9.
2
Combination microRNA-based cellular reprogramming with paclitaxel enhances therapeutic efficacy in a relapsed and multidrug-resistant model of epithelial ovarian cancer.基于微小RNA的细胞重编程与紫杉醇联合应用可增强复发性和多药耐药性上皮性卵巢癌模型的治疗效果。
Mol Ther Oncolytics. 2022 Mar 15;25:57-68. doi: 10.1016/j.omto.2022.03.005. eCollection 2022 Jun 16.
3
Identification of the most common BRCA alterations through analysis of germline mutation databases: Is droplet digital PCR an additional strategy for the assessment of such alterations in breast and ovarian cancer families?
通过分析种系突变数据库鉴定最常见的 BRCA 改变:液滴数字 PCR 是否是评估乳腺癌和卵巢癌家族中此类改变的附加策略?
Int J Oncol. 2022 May;60(5). doi: 10.3892/ijo.2022.5349. Epub 2022 Apr 6.
4
Targeted delivery of exosomal miR-484 reprograms tumor vasculature for chemotherapy sensitization.外泌体 miR-484 的靶向递送重编程肿瘤血管以增强化疗敏感性。
Cancer Lett. 2022 Apr 1;530:45-58. doi: 10.1016/j.canlet.2022.01.011. Epub 2022 Jan 18.
5
MiR-149-3p promotes the cisplatin resistance and EMT in ovarian cancer through downregulating TIMP2 and CDKN1A.miR-149-3p 通过下调 TIMP2 和 CDKN1A 促进卵巢癌细胞顺铂耐药和 EMT。
J Ovarian Res. 2021 Nov 19;14(1):165. doi: 10.1186/s13048-021-00919-5.
6
Differences in Ovarian and Other Cancers Risks by Population and Mutation Location.按人群和突变位置划分的卵巢癌和其他癌症风险的差异。
Genes (Basel). 2021 Jul 8;12(7):1050. doi: 10.3390/genes12071050.
7
Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries.《全球癌症统计数据 2020:全球 185 个国家和地区 36 种癌症的发病率和死亡率估计》。
CA Cancer J Clin. 2021 May;71(3):209-249. doi: 10.3322/caac.21660. Epub 2021 Feb 4.
8
The Effects of Combination of Mimic miR-155-5p and Antagonist miR-324-5p Encapsulated Chitosan in Ovarian Cancer SKOV3.壳聚糖包裹 mimic miR-155-5p 和拮抗剂 miR-324-5p 对卵巢癌 SKOV3 的影响。
Asian Pac J Cancer Prev. 2020 Sep 1;21(9):2603-2608. doi: 10.31557/APJCP.2020.21.9.2603.
9
Roles of microRNAs in Ovarian Cancer Tumorigenesis: Two Decades Later, What Have We Learned?微小RNA在卵巢癌肿瘤发生中的作用:二十年后,我们学到了什么?
Front Oncol. 2020 Jul 21;10:1084. doi: 10.3389/fonc.2020.01084. eCollection 2020.
10
MicroRNA-302 represses epithelial-mesenchymal transition and cisplatin resistance by regulating ATAD2 in ovarian carcinoma.MicroRNA-302 通过调控卵巢癌细胞中的 ATAD2 抑制上皮-间质转化和顺铂耐药性。
Exp Cell Res. 2020 Nov 1;396(1):112241. doi: 10.1016/j.yexcr.2020.112241. Epub 2020 Aug 21.