• 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

宫颈癌的发生、化疗耐药及其治疗:miRNA 参与的一个快照。

Cervical cancer development, chemoresistance, and therapy: a snapshot of involvement of microRNA.

机构信息

School of Biotechnology, Kalinga Institute of Industrial Technology (KIIT), Deemed To Be University, Bhubaneswar, Odisha, 751024, India.

出版信息

Mol Cell Biochem. 2021 Dec;476(12):4363-4385. doi: 10.1007/s11010-021-04249-4. Epub 2021 Aug 28.

DOI:10.1007/s11010-021-04249-4
PMID:34453645
Abstract

Cervical cancer (CC) is one of the leading causes of death in women due to cancer and a major concern in the developing world. Persistent human papilloma virus (HPV) infection is the major causative agent for CC. Besides HPV infection, genetic and epigenetic factors including microRNA (miRNA) also contribute to the malignant transformation. Earlier studies have revealed that miRNAs participate in cell proliferation, invasion and metastasis, angiogenesis, and chemoresistance processes by binding and inversely regulating the target oncogenes or tumor suppressor genes. Based on functions and mechanistic insights, miRNAs have been identified as cellular modulators that have an enormous role in diagnosis, prognosis, and cancer therapy. Signatures of miRNA could be used as diagnostic markers which are necessary for early diagnosis and management of CC. The therapeutic potential of miRNAs has been shown in CC; however, more comprehensive clinical trials are required for the clinical translation of miRNA-based diagnostics and therapeutics. Understanding the molecular mechanism of miRNAs and their target genes has been useful to develop miRNA-based therapeutic strategies for CC and overcome chemoresistance. In this review, we summarize the role of miRNAs in the development, progression, and metastasis of CC as well as chemoresistance. Further, we discuss the diagnostic and therapeutic potential of miRNAs to overcome chemoresistance and treatment of CC.

摘要

宫颈癌(CC)是癌症导致女性死亡的主要原因之一,也是发展中国家的主要关注点。持续性人乳头瘤病毒(HPV)感染是 CC 的主要致病因素。除 HPV 感染外,遗传和表观遗传因素,包括 microRNA(miRNA),也有助于恶性转化。早期研究表明,miRNA 通过结合并反向调节靶原癌基因或肿瘤抑制基因,参与细胞增殖、侵袭和转移、血管生成和化疗耐药过程。基于功能和机制的见解,miRNA 已被确定为细胞调节剂,在诊断、预后和癌症治疗中具有重要作用。miRNA 的特征可以用作诊断标志物,这对于 CC 的早期诊断和管理是必要的。miRNA 在 CC 中的治疗潜力已经得到证实;然而,需要更多全面的临床试验来将 miRNA 为基础的诊断和治疗方法进行临床转化。了解 miRNA 及其靶基因的分子机制有助于开发基于 miRNA 的 CC 治疗策略并克服化疗耐药性。在这篇综述中,我们总结了 miRNA 在 CC 的发展、进展和转移以及化疗耐药性中的作用。此外,我们讨论了 miRNA 在克服化疗耐药性和治疗 CC 方面的诊断和治疗潜力。

相似文献

1
Cervical cancer development, chemoresistance, and therapy: a snapshot of involvement of microRNA.宫颈癌的发生、化疗耐药及其治疗:miRNA 参与的一个快照。
Mol Cell Biochem. 2021 Dec;476(12):4363-4385. doi: 10.1007/s11010-021-04249-4. Epub 2021 Aug 28.
2
The Role of microRNA Expression and DNA Methylation in HPV-Related Cervical Cancer: A Systematic Review.微小RNA表达和DNA甲基化在人乳头瘤病毒相关宫颈癌中的作用:一项系统综述
Int J Mol Sci. 2024 Nov 26;25(23):12714. doi: 10.3390/ijms252312714.
3
Differential Expression of MicroRNAs in Uterine Cervical Cancer and Its Implications in Carcinogenesis; An Integrative Approach.微小 RNA 在子宫颈癌中的差异表达及其在癌变中的意义;一种综合方法。
Int J Gynecol Cancer. 2018 Mar;28(3):553-562. doi: 10.1097/IGC.0000000000001203.
4
Human papilloma virus, DNA methylation and microRNA expression in cervical cancer (Review).人乳头瘤病毒、宫颈癌中的 DNA 甲基化和 microRNA 表达(综述)。
Oncol Rep. 2014 Jun;31(6):2467-76. doi: 10.3892/or.2014.3142. Epub 2014 Apr 16.
5
[The role of microRNAs in the pathogenesis of cervical cancer and its relationship to HPV].[微小RNA在宫颈癌发病机制中的作用及其与人类乳头瘤病毒的关系]
Sheng Li Ke Xue Jin Zhan. 2012 Aug;43(4):251-6.
6
MicroRNA-18a targeting of the STK4/MST1 tumour suppressor is necessary for transformation in HPV positive cervical cancer.微小 RNA-18a 靶向 STK4/MST1 肿瘤抑制因子对于 HPV 阳性宫颈癌的转化是必要的。
PLoS Pathog. 2020 Jun 18;16(6):e1008624. doi: 10.1371/journal.ppat.1008624. eCollection 2020 Jun.
7
Molecular markers predicting the progression and prognosis of human papillomavirus-induced cervical lesions to cervical cancer.预测人乳头瘤病毒诱导的宫颈病变向宫颈癌进展和预后的分子标志物。
J Cancer Res Clin Oncol. 2023 Aug;149(10):8077-8086. doi: 10.1007/s00432-023-04710-5. Epub 2023 Mar 31.
8
miR-10b Downregulated by DNA Methylation Acts as a Tumor Suppressor in HPV-Positive Cervical Cancer via Targeting Tiam1.通过靶向Tiam1,DNA甲基化下调的miR-10b在人乳头瘤病毒阳性宫颈癌中作为肿瘤抑制因子发挥作用。
Cell Physiol Biochem. 2018;51(4):1763-1777. doi: 10.1159/000495680. Epub 2018 Nov 30.
9
Novel MicroRNA signatures in HPV-mediated cervical carcinogenesis in Indian women.印度女性人乳头瘤病毒介导的宫颈癌发生中的新型微小RNA特征
Tumour Biol. 2016 Apr;37(4):4585-95. doi: 10.1007/s13277-015-4248-7. Epub 2015 Oct 27.
10
HDAC6 suppresses microRNA-199a transcription and augments HPV-positive cervical cancer progression through Wnt5a upregulation.组蛋白去乙酰化酶 6 通过上调 Wnt5a 抑制 microRNA-199a 的转录,从而增强 HPV 阳性宫颈癌的进展。
Int J Biochem Cell Biol. 2021 Jul;136:106000. doi: 10.1016/j.biocel.2021.106000. Epub 2021 Apr 29.

引用本文的文献

1
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.
2
Long non-coding RNA H19 promotes cervical cancer development via targeting the microRNA-140/ALDH1A1 axis.长链非编码RNA H19通过靶向微小RNA-140/醛脱氢酶1A1轴促进宫颈癌发展。
Eur J Med Res. 2025 Feb 12;30(1):95. doi: 10.1186/s40001-025-02350-8.
3
Alterations in miRNA Expression and Their Role in the Pathogenesis of Cervical Cancer.

本文引用的文献

1
MicroRNA-362-3p Inhibits Migration and Invasion via Targeting BCAP31 in Cervical Cancer.微小RNA-362-3p通过靶向宫颈癌中的BCAP31抑制迁移和侵袭。
Front Mol Biosci. 2020 Jun 9;7:107. doi: 10.3389/fmolb.2020.00107. eCollection 2020.
2
miR-16-5p/PDK4-Mediated Metabolic Reprogramming Is Involved in Chemoresistance of Cervical Cancer.miR-16-5p/PDK4介导的代谢重编程参与宫颈癌的化疗耐药
Mol Ther Oncolytics. 2020 May 23;17:509-517. doi: 10.1016/j.omto.2020.05.008. eCollection 2020 Jun 26.
3
Identification of Prognostic miRNA Signature and Lymph Node Metastasis-Related Key Genes in Cervical Cancer.
miRNA 表达的改变及其在宫颈癌发病机制中的作用。
Asian Pac J Cancer Prev. 2024 Oct 1;25(10):3533-3541. doi: 10.31557/APJCP.2024.25.10.3533.
4
Therapeutic Strategies in Advanced Cervical Cancer Detection, Prevention and Treatment.晚期宫颈癌的检测、预防与治疗中的治疗策略
Onco Targets Ther. 2024 Sep 25;17:785-801. doi: 10.2147/OTT.S475132. eCollection 2024.
5
Understanding the role of miRNAs in cervical cancer pathogenesis and therapeutic responses.了解微小RNA在宫颈癌发病机制及治疗反应中的作用。
Front Cell Dev Biol. 2024 Aug 28;12:1397945. doi: 10.3389/fcell.2024.1397945. eCollection 2024.
6
Overview of miR-106a Regulatory Roles: from Cancer to Aging.miR-106a调控作用概述:从癌症到衰老
Bioengineering (Basel). 2023 Jul 27;10(8):892. doi: 10.3390/bioengineering10080892.
7
Knockdown of miR-24 Suppressed the Tumor Growth of Cervical Carcinoma Through Regulating PTEN/PI3K/AKT Signaling Pathway.miR-24 敲低通过调控 PTEN/PI3K/AKT 信号通路抑制宫颈癌的肿瘤生长。
Biochem Genet. 2024 Apr;62(2):1277-1290. doi: 10.1007/s10528-023-10491-w. Epub 2023 Aug 17.
8
Human Papilloma Virus: An Unraveled Enigma of Universal Burden of Malignancies.人乳头瘤病毒:解开恶性肿瘤全球负担之谜
Pathogens. 2023 Apr 6;12(4):564. doi: 10.3390/pathogens12040564.
9
Recent Updates on the Role of the MicroRNA-10 Family in Gynecological Malignancies.微小RNA-10家族在妇科恶性肿瘤中作用的最新进展
J Oncol. 2022 Dec 19;2022:1544648. doi: 10.1155/2022/1544648. eCollection 2022.
10
Resveratrol against Cervical Cancer: Evidence from In Vitro and In Vivo Studies.白藜芦醇抗宫颈癌:来自体外和体内研究的证据。
Nutrients. 2022 Dec 10;14(24):5273. doi: 10.3390/nu14245273.
宫颈癌中预后性miRNA特征及淋巴结转移相关关键基因的鉴定
Front Pharmacol. 2020 May 8;11:544. doi: 10.3389/fphar.2020.00544. eCollection 2020.
4
MicroRNA-21 promotes cell metastasis in cervical cancer through modulating epithelial-mesenchymal transition.微小RNA-21通过调节上皮-间质转化促进宫颈癌细胞转移。
Oncol Lett. 2020 Apr;19(4):3289-3295. doi: 10.3892/ol.2020.11438. Epub 2020 Mar 3.
5
MiR-23b-3p reduces the proliferation, migration and invasion of cervical cancer cell lines via the reduction of c-Met expression.miR-23b-3p 通过降低 c-Met 表达来减少宫颈癌细胞系的增殖、迁移和侵袭。
Sci Rep. 2020 Feb 24;10(1):3256. doi: 10.1038/s41598-020-60143-x.
6
Human Papillomavirus E6 and E7: The Cervical Cancer Hallmarks and Targets for Therapy.人乳头瘤病毒E6和E7:宫颈癌的标志及治疗靶点
Front Microbiol. 2020 Jan 21;10:3116. doi: 10.3389/fmicb.2019.03116. eCollection 2019.
7
MicroRNA-708 Suppresses Cell Proliferation and Enhances Chemosensitivity of Cervical Cancer Cells to cDDP by Negatively Targeting Timeless.微小RNA-708通过负向靶向Timeless抑制宫颈癌细胞增殖并增强其对顺铂的化疗敏感性。
Onco Targets Ther. 2020 Jan 9;13:225-235. doi: 10.2147/OTT.S227015. eCollection 2020.
8
microRNA-499a promotes the progression and chemoresistance of cervical cancer cells by targeting SOX6.microRNA-499a 通过靶向 SOX6 促进宫颈癌细胞的进展和化疗耐药性。
Apoptosis. 2020 Apr;25(3-4):205-216. doi: 10.1007/s10495-019-01588-y.
9
Role of miR-221/222 in Tumor Development and the Underlying Mechanism.miR-221/222在肿瘤发展中的作用及潜在机制
J Oncol. 2019 Dec 24;2019:7252013. doi: 10.1155/2019/7252013. eCollection 2019.
10
MicroRNA-497-5p Induces Cell Cycle Arrest Of Cervical Cancer Cells In S Phase By Targeting CBX4.微小RNA-497-5p通过靶向CBX4诱导宫颈癌细胞在S期发生细胞周期阻滞。
Onco Targets Ther. 2019 Dec 2;12:10535-10545. doi: 10.2147/OTT.S210059. eCollection 2019.