• 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

长链非编码RNA作为癌症中翻译后修饰关键调节因子的新见解:机制与治疗潜力

Novel insights into lncRNAs as key regulators of post-translational modifications in cancer: mechanisms and therapeutic potential.

作者信息

Han Yaqian, Li Shizhen, Oyang Linda, Cui Shiwen, Zhang Wenlong, Yang Wenjuan, Peng Mingjing, Tan Shiming, Xia Longzheng, Lin Jinguan, Xu Xuemeng, Wu Nayiyuan, Jiang Xianjie, Peng Qiu, Tang Yanyan, Luo Xia, Liao Qianjin, Zhou Yujuan

机构信息

The Affiliated Cancer Hospital of Xiangya School of Medicine, Hunan Key Laboratory of Cancer Metabolism Changsha, Central South University, Hunan Cancer Hospital, 283 Tongzipo Road, Changsha, Changsha, Hunan, 410013, China.

Department of Oncology, Hunan Provincial People's Hospital (The First- Affiliated Hospital of Hunan Normal University), 61 Jiefang West Road, Changsha, Hunan, 410005, China.

出版信息

Cell Oncol (Dordr). 2025 Jul 2. doi: 10.1007/s13402-025-01086-1.

DOI:10.1007/s13402-025-01086-1
PMID:40601247
Abstract

Abnormal post-translational modifications (PTMs) play a crucial role in tumor initiation and progression. However, the mechanisms by which lncRNAs, as emerging epigenetic regulators, mediate PTMs remain largely unexplored. This review provides a comprehensive summary of the latest research on the interplay between lncRNA-mediated PTMs and tumorigenesis. We delve into the molecular mechanisms underlying these interactions, focusing on how lncRNAs regulate PTMs to influence tumor progression. We place particular emphasis on the lncRNA-mediated PTMs as a driver of therapeutic resistance, shedding light on its potential as a novel target for cancer intervention. Furthermore, we highlight the therapeutic potential of targeting lncRNA-PTM networks, emphasizing novel RNA-based strategies and their clinical relevance in cancer treatment. We believe that an in-depth understanding of lncRNA-mediated PTMs could uncover novel therapeutic targets, paving the way for innovative approaches in cancer diagnosis and treatment.

摘要

异常的翻译后修饰(PTMs)在肿瘤的发生和发展中起着关键作用。然而,作为新兴的表观遗传调节因子,长链非编码RNA(lncRNAs)介导PTMs的机制在很大程度上仍未被探索。本综述全面总结了lncRNA介导的PTMs与肿瘤发生之间相互作用的最新研究。我们深入探讨了这些相互作用的分子机制,重点关注lncRNAs如何调节PTMs以影响肿瘤进展。我们特别强调lncRNA介导的PTMs作为治疗抗性驱动因素的作用,揭示其作为癌症干预新靶点的潜力。此外,我们强调靶向lncRNA-PTM网络的治疗潜力,强调基于RNA的新策略及其在癌症治疗中的临床相关性。我们相信,深入了解lncRNA介导的PTMs可以发现新的治疗靶点,为癌症诊断和治疗的创新方法铺平道路。

相似文献

1
Novel insights into lncRNAs as key regulators of post-translational modifications in cancer: mechanisms and therapeutic potential.长链非编码RNA作为癌症中翻译后修饰关键调节因子的新见解:机制与治疗潜力
Cell Oncol (Dordr). 2025 Jul 2. doi: 10.1007/s13402-025-01086-1.
2
Targeting post-translational modifications: novel insights into bone metabolic diseases.靶向翻译后修饰:对骨代谢疾病的新见解。
J Adv Res. 2025 Jun 13. doi: 10.1016/j.jare.2025.06.020.
3
Regulatory mechanisms and clinical implications of PIWI-interacting RNAs (piRNAs) in major digestive tract cancers.PIWI相互作用RNA(piRNA)在主要消化道癌症中的调控机制及临床意义
Cancer Cell Int. 2025 Jul 2;25(1):244. doi: 10.1186/s12935-025-03889-6.
4
RNA modifications in female reproductive physiology and disease: emerging roles and clinical implications.RNA修饰在女性生殖生理与疾病中的作用:新出现的作用及临床意义
Hum Reprod Update. 2025 Mar 27. doi: 10.1093/humupd/dmaf005.
5
Cuproptosis: a novel therapeutic mechanism in lung cancer.铜死亡:肺癌中的一种新型治疗机制。
Cancer Cell Int. 2025 Jun 24;25(1):231. doi: 10.1186/s12935-025-03864-1.
6
How lived experiences of illness trajectories, burdens of treatment, and social inequalities shape service user and caregiver participation in health and social care: a theory-informed qualitative evidence synthesis.疾病轨迹的生活经历、治疗负担和社会不平等如何影响服务使用者和照顾者参与健康和社会护理:一项基于理论的定性证据综合分析
Health Soc Care Deliv Res. 2025 Jun;13(24):1-120. doi: 10.3310/HGTQ8159.
7
Decoding the role of novel long noncoding RNAs lnc-SLC6A12-1:3 and lnc-SLC6A12-7:5 in regulating the expression of GAD1 and SLC6A12 in cholangiocarcinoma.解码新型长链非编码RNA lnc-SLC6A12-1:3和lnc-SLC6A12-7:5在调节胆管癌中GAD1和SLC6A12表达方面的作用。
Comput Biol Chem. 2025 Jun 20;119:108562. doi: 10.1016/j.compbiolchem.2025.108562.
8
Stigma Management Strategies of Autistic Social Media Users.自闭症社交媒体用户的污名管理策略
Autism Adulthood. 2025 May 28;7(3):273-282. doi: 10.1089/aut.2023.0095. eCollection 2025 Jun.
9
Factors that influence parents' and informal caregivers' views and practices regarding routine childhood vaccination: a qualitative evidence synthesis.影响父母和非正式照顾者对常规儿童疫苗接种看法和做法的因素:定性证据综合分析。
Cochrane Database Syst Rev. 2021 Oct 27;10(10):CD013265. doi: 10.1002/14651858.CD013265.pub2.
10
Survivor, family and professional experiences of psychosocial interventions for sexual abuse and violence: a qualitative evidence synthesis.性虐待和暴力的心理社会干预的幸存者、家庭和专业人员的经验:定性证据综合。
Cochrane Database Syst Rev. 2022 Oct 4;10(10):CD013648. doi: 10.1002/14651858.CD013648.pub2.

本文引用的文献

1
Transcriptome-scale RNA-targeting CRISPR screens reveal essential lncRNAs in human cells.转录组规模的RNA靶向CRISPR筛选揭示了人类细胞中的必需长链非编码RNA。
Cell. 2024 Dec 26;187(26):7637-7654.e29. doi: 10.1016/j.cell.2024.10.021. Epub 2024 Nov 11.
2
HCP5 Derived Novel Microprotein Triggers Progression of Gastric Cancer through Regulating Ferroptosis.HCP5衍生的新型微蛋白通过调节铁死亡触发胃癌进展。
Adv Sci (Weinh). 2024 Dec;11(46):e2407012. doi: 10.1002/advs.202407012. Epub 2024 Oct 24.
3
Altered glycosylation in cancer: molecular functions and therapeutic potential.
癌症中的糖基化修饰改变:分子功能与治疗潜力。
Cancer Commun (Lond). 2024 Nov;44(11):1316-1336. doi: 10.1002/cac2.12610. Epub 2024 Sep 21.
4
Direct cytosolic delivery of siRNA via cell membrane fusion using cholesterol-enriched exosomes.利用富含胆固醇的外泌体通过细胞膜融合实现小干扰RNA的直接胞质递送。
Nat Nanotechnol. 2024 Dec;19(12):1858-1868. doi: 10.1038/s41565-024-01785-0. Epub 2024 Sep 19.
5
Exosomal SLC16A1-AS1-induced M2 macrophages polarization facilitates hepatocellular carcinoma progression.外泌体 SLC16A1-AS1 诱导的 M2 型巨噬细胞极化促进肝癌进展。
Int J Biol Sci. 2024 Aug 12;20(11):4341-4363. doi: 10.7150/ijbs.94440. eCollection 2024.
6
ATR/Chk1 interacting lncRNA modulates DNA damage response to induce breast cancer chemoresistance.ATR/Chk1相互作用的长链非编码RNA调节DNA损伤反应以诱导乳腺癌化疗耐药。
Cell Insight. 2024 Jul 14;3(5):100183. doi: 10.1016/j.cellin.2024.100183. eCollection 2024 Oct.
7
Hypoxia-induced downregulation of PGK1 crotonylation promotes tumorigenesis by coordinating glycolysis and the TCA cycle.缺氧诱导的 PGK1 琥珀酰化下调通过协调糖酵解和三羧酸循环促进肿瘤发生。
Nat Commun. 2024 Aug 12;15(1):6915. doi: 10.1038/s41467-024-51232-w.
8
NBS1 lactylation is required for efficient DNA repair and chemotherapy resistance.高效的DNA修复和化疗耐药性需要NBS1乳酸化。
Nature. 2024 Jul;631(8021):663-669. doi: 10.1038/s41586-024-07620-9. Epub 2024 Jul 3.
9
Ponatinib vs Imatinib in Frontline Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia: A Randomized Clinical Trial.Ponatinib 对比伊马替尼用于一线治疗费城染色体阳性急性淋巴细胞白血病:一项随机临床试验。
JAMA. 2024 Jun 4;331(21):1814-1823. doi: 10.1001/jama.2024.4783.
10
Loss of lncRNA LINC01056 leads to sorafenib resistance in HCC.长链非编码 RNA LINC01056 的缺失导致 HCC 对索拉非尼产生耐药性。
Mol Cancer. 2024 Apr 6;23(1):74. doi: 10.1186/s12943-024-01988-y.