• 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

罗恩受体酪氨酸激酶信号转导作为治疗靶点。

Ron receptor tyrosine kinase signaling as a therapeutic target.

机构信息

University of Cincinnati College of Medicine, Cincinnati Veterans Affairs Medical Center, Department of Cancer and Cell Biology, OH 45267-0521, USA.

出版信息

Expert Opin Ther Targets. 2012 Sep;16(9):921-31. doi: 10.1517/14728222.2012.710200. Epub 2012 Jul 26.

DOI:10.1517/14728222.2012.710200
PMID:22834780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4075176/
Abstract

INTRODUCTION

Since its discovery nearly 20 years ago, the Ron receptor tyrosine kinase has been extensively studied. These studies have elucidated many of the major signaling pathways activated by Ron. In the context of the inflammation and cancer, studies have shown that Ron plays differential roles; Ron activation limits the inflammatory response, whereas in cancer, Ron activation is associated with increased metastases and poor prognosis.

AREAS COVERED

This review discusses the current literature with regard to Ron signaling and consequences of its activation in cancer as well as its role in cancer therapy. Further, we discuss the mechanisms by which Ron influences the inflammatory response and its role in chronic inflammatory diseases. Finally, we discuss Ron's connection between chronic inflammation and progression to cancer.

EXPERT OPINION

The complex nature of Ron's signaling paradigm necessitates additional studies to understand the pathways by which Ron is functioning and how these differ in inflammation and cancer. This will be vital to understanding the impact that Ron signaling has in disease states. Additional studies of targeted therapies, either alone or in conjunction with current therapies are needed to determine if inhibition of Ron signaling will provide long-term benefits to cancer patients.

摘要

简介

近 20 年前发现 Ron 受体酪氨酸激酶以来,人们对其进行了广泛研究。这些研究阐明了 Ron 激活的许多主要信号通路。在炎症和癌症的背景下,研究表明 Ron 发挥了不同的作用;Ron 激活限制了炎症反应,而在癌症中,Ron 激活与转移增加和预后不良有关。

涵盖领域

本文综述了 Ron 信号及其在癌症中激活的后果以及在癌症治疗中的作用的最新文献。此外,我们还讨论了 Ron 影响炎症反应的机制及其在慢性炎症性疾病中的作用。最后,我们讨论了 Ron 与慢性炎症向癌症进展之间的联系。

专家意见

Ron 信号的复杂性质需要进一步研究,以了解 Ron 发挥作用的途径以及这些途径在炎症和癌症中的差异。这对于了解 Ron 信号在疾病状态中的影响至关重要。需要进一步研究针对 Ron 的靶向治疗,无论是单独使用还是与现有治疗方法联合使用,以确定抑制 Ron 信号是否会为癌症患者带来长期益处。

相似文献

1
Ron receptor tyrosine kinase signaling as a therapeutic target.罗恩受体酪氨酸激酶信号转导作为治疗靶点。
Expert Opin Ther Targets. 2012 Sep;16(9):921-31. doi: 10.1517/14728222.2012.710200. Epub 2012 Jul 26.
2
Preclinical Efficacy of Ron Kinase Inhibitors Alone and in Combination with PI3K Inhibitors for Treatment of sfRon-Expressing Breast Cancer Patient-Derived Xenografts.Ron激酶抑制剂单独及与PI3K抑制剂联合用于治疗表达sfRon的乳腺癌患者来源异种移植瘤的临床前疗效
Clin Cancer Res. 2015 Dec 15;21(24):5588-600. doi: 10.1158/1078-0432.CCR-14-3283. Epub 2015 Aug 19.
3
RON Signaling Is a Key Mediator of Tumor Progression in Many Human Cancers.RON信号传导是多种人类癌症肿瘤进展的关键介质。
Cold Spring Harb Symp Quant Biol. 2016;81:177-188. doi: 10.1101/sqb.2016.81.031377. Epub 2017 Jan 5.
4
A potential signaling axis between RON kinase receptor and hypoxia-inducible factor-1 alpha in pancreatic cancer.RON 激酶受体与缺氧诱导因子-1α在胰腺癌中的潜在信号轴。
Mol Carcinog. 2021 Nov;60(11):734-745. doi: 10.1002/mc.23339. Epub 2021 Aug 4.
5
Multiple variants of the RON receptor tyrosine kinase: biochemical properties, tumorigenic activities, and potential drug targets.RON受体酪氨酸激酶的多种变体:生化特性、致瘤活性及潜在药物靶点。
Cancer Lett. 2007 Nov 18;257(2):157-64. doi: 10.1016/j.canlet.2007.08.007. Epub 2007 Sep 21.
6
The ron receptor tyrosine kinase: a key regulator of inflammation and cancer progression.Ron受体酪氨酸激酶:炎症和癌症进展的关键调节因子。
Crit Rev Immunol. 2013;33(6):549-74. doi: 10.1615/critrevimmunol.2013007953.
7
RON and MET Co-overexpression Are Significant Pathological Characteristics of Poor Survival and Therapeutic Targets of Tyrosine Kinase Inhibitors in Triple-Negative Breast Cancer.RON 和 MET 共表达是三阴性乳腺癌不良生存的重要病理特征,也是酪氨酸激酶抑制剂治疗靶点。
Cancer Res Treat. 2020 Jul;52(3):973-986. doi: 10.4143/crt.2019.726. Epub 2020 Apr 22.
8
Ron receptor tyrosine kinase activation confers resistance to tamoxifen in breast cancer cell lines.罗恩受体酪氨酸激酶的激活赋予乳腺癌细胞系对他莫昔芬的耐药性。
Neoplasia. 2010 Aug;12(8):650-8. doi: 10.1593/neo.10476.
9
Met-related receptor tyrosine kinase Ron in tumor growth and metastasis.与Met相关的受体酪氨酸激酶Ron在肿瘤生长和转移中的作用
Adv Cancer Res. 2008;100:1-33. doi: 10.1016/S0065-230X(08)00001-8.
10
Recepteur d'origine nantais tyrosine kinase is a direct target of hypoxia-inducible factor-1alpha-mediated invasion of breast carcinoma cells.源自南特的酪氨酸激酶受体是缺氧诱导因子-1α介导的乳腺癌细胞侵袭的直接靶点。
J Biol Chem. 2009 May 22;284(21):14001-10. doi: 10.1074/jbc.M809320200. Epub 2009 Mar 23.

引用本文的文献

1
MSP-RON signaling in liver pathobiology and as an emerging therapeutic target: a review of the current evidence.MSP-RON信号通路在肝脏病理生物学中的作用及作为新兴治疗靶点的研究现状:现有证据综述
Cell Commun Signal. 2025 Aug 28;23(1):385. doi: 10.1186/s12964-025-02407-5.
2
An Introduction and Overview of RON Receptor Tyrosine Kinase Signaling.RON 受体酪氨酸激酶信号概述与介绍。
Genes (Basel). 2023 Feb 17;14(2):517. doi: 10.3390/genes14020517.
3
Regulation of Kinase Signaling Pathways by α6β4-Integrins and Plectin in Prostate Cancer.

本文引用的文献

1
Multiple associations between a broad spectrum of autoimmune diseases, chronic inflammatory diseases and cancer.多种自身免疫性疾病、慢性炎症性疾病和癌症之间存在广泛关联。
Anticancer Res. 2012 Apr;32(4):1119-36.
2
Conditional deletion of β-catenin in mammary epithelial cells of Ron receptor, Mst1r, overexpressing mice alters mammary tumorigenesis.Ron 受体、Mst1r 过表达小鼠乳腺上皮细胞中β-catenin 的条件性缺失改变了乳腺肿瘤发生。
Endocrinology. 2012 Jun;153(6):2735-46. doi: 10.1210/en.2011-1543. Epub 2012 Apr 2.
3
Antiangiogenic therapy--evolving view based on clinical trial results.
α6β4整合素和网蛋白对前列腺癌激酶信号通路的调控
Cancers (Basel). 2022 Dec 27;15(1):149. doi: 10.3390/cancers15010149.
4
Genetic Influences in Cancer-Associated Myositis.癌症相关肌炎的遗传影响。
Arthritis Rheumatol. 2023 Feb;75(2):153-163. doi: 10.1002/art.42345. Epub 2022 Dec 20.
5
RUNX1/EGFR pathway contributes to STAT3 activation and tumor growth caused by hyperactivated mTORC1.RUNX1/表皮生长因子受体(EGFR)通路促进了由过度激活的哺乳动物雷帕霉素靶蛋白复合体1(mTORC1)所引起的信号转导和转录激活因子3(STAT3)的激活以及肿瘤生长。
Mol Ther Oncolytics. 2021 Oct 28;23:387-401. doi: 10.1016/j.omto.2021.10.009. eCollection 2021 Dec 17.
6
Macrophage-mediated RON signaling supports breast cancer growth and progression through modulation of IL-35.巨噬细胞介导的 RON 信号通过调节 IL-35 支持乳腺癌的生长和进展。
Oncogene. 2022 Jan;41(3):321-333. doi: 10.1038/s41388-021-02091-y. Epub 2021 Nov 6.
7
RON in hepatobiliary and pancreatic cancers: Pathogenesis and potential therapeutic targets.RON 在肝胆胰腺肿瘤中的作用:发病机制与潜在治疗靶点。
World J Gastroenterol. 2021 May 28;27(20):2507-2520. doi: 10.3748/wjg.v27.i20.2507.
8
NanoString technology distinguishes anti-TIF-1γ from anti-Mi-2 dermatomyositis patients.NanoString 技术可区分抗 TIF-1γ 与抗 Mi-2 皮肌炎患者。
Brain Pathol. 2021 May;31(3):e12957. doi: 10.1111/bpa.12957.
9
The HNRNPA2B1-MST1R-Akt axis contributes to epithelial-to-mesenchymal transition in head and neck cancer.HNRNPA2B1-MST1R-Akt 轴促进头颈部癌症的上皮间质转化。
Lab Invest. 2020 Dec;100(12):1589-1601. doi: 10.1038/s41374-020-0466-8. Epub 2020 Jul 15.
10
MST1R (RON) expression is a novel prognostic biomarker for metastatic progression in breast cancer patients.MST1R(RON)表达是乳腺癌患者转移进展的新型预后生物标志物。
Breast Cancer Res Treat. 2020 Jun;181(3):529-540. doi: 10.1007/s10549-020-05653-y. Epub 2020 Apr 27.
抗血管生成治疗——基于临床试验结果的不断变化的观点。
Nat Rev Clin Oncol. 2012 Feb 14;9(5):297-303. doi: 10.1038/nrclinonc.2012.8.
4
The RON-receptor regulates pancreatic cancer cell migration through phosphorylation-dependent breakdown of the hemidesmosome.RON 受体通过依赖磷酸化的半桥粒崩解调控胰腺癌细胞迁移。
Int J Cancer. 2012 Oct 15;131(8):1744-54. doi: 10.1002/ijc.27447. Epub 2012 Mar 8.
5
Macrophage-stimulating protein polymorphism rs3197999 is associated with a gain of function: implications for inflammatory bowel disease.巨噬细胞刺激蛋白多态性 rs3197999 与功能获得有关:对炎症性肠病的影响。
Genes Immun. 2012 Jun;13(4):321-7. doi: 10.1038/gene.2011.88. Epub 2012 Jan 12.
6
Protein characterization of a candidate mechanism SNP for Crohn's disease: the macrophage stimulating protein R689C substitution.候选机制 SNP 对克罗恩病的蛋白特性分析:巨噬细胞刺激蛋白 R689C 取代。
PLoS One. 2011;6(11):e27269. doi: 10.1371/journal.pone.0027269. Epub 2011 Nov 7.
7
Sustained expression of the RON receptor tyrosine kinase by pancreatic cancer stem cells as a potential targeting moiety for antibody-directed chemotherapeutics.胰腺癌干细胞中 RON 受体酪氨酸激酶的持续表达可作为抗体导向化疗的潜在靶向部分。
Mol Pharm. 2011 Dec 5;8(6):2310-9. doi: 10.1021/mp200193u. Epub 2011 Nov 1.
8
Ron receptor overexpression in the murine prostate induces prostate intraepithelial neoplasia.罗恩受体在小鼠前列腺中的过表达诱导前列腺上皮内瘤形成。
Cancer Lett. 2012 Jan 1;314(1):92-101. doi: 10.1016/j.canlet.2011.09.021. Epub 2011 Sep 24.
9
Managing resistance in chronic myeloid leukemia.慢性髓性白血病的耐药管理。
Blood Rev. 2011 Nov;25(6):279-90. doi: 10.1016/j.blre.2011.09.001. Epub 2011 Oct 6.
10
Regulation of macrophage arginase expression and tumor growth by the Ron receptor tyrosine kinase.Ron 受体酪氨酸激酶对巨噬细胞精氨酸酶表达和肿瘤生长的调控。
J Immunol. 2011 Sep 1;187(5):2181-92. doi: 10.4049/jimmunol.1003460. Epub 2011 Aug 1.