• 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

相似文献

1
Targeting IGF1R pathway in cancer with microRNAs: How close are we?用 microRNAs 靶向癌症中的 IGF1R 通路:我们有多接近?
RNA Biol. 2018 Mar 4;15(3):320-326. doi: 10.1080/15476286.2017.1338240. Epub 2018 Feb 1.
2
Co-targeting of IGF1R/mTOR pathway by miR-497 and miR-99a impairs hepatocellular carcinoma development.miR-497和miR-99a对IGF1R/mTOR通路的共同靶向作用会损害肝细胞癌的发展。
Oncotarget. 2017 Jul 18;8(29):47984-47997. doi: 10.18632/oncotarget.18207.
3
Implication of epithelial-mesenchymal transition in IGF1R-induced resistance to EGFR-TKIs in advanced non-small cell lung cancer.上皮-间质转化在IGF1R诱导的晚期非小细胞肺癌对EGFR-TKIs耐药中的作用
Oncotarget. 2015 Dec 29;6(42):44332-45. doi: 10.18632/oncotarget.6293.
4
MiR-1294 confers cisplatin resistance in ovarian Cancer cells by targeting IGF1R.miR-1294 通过靶向 IGF1R 赋予卵巢癌细胞顺铂耐药性。
Biomed Pharmacother. 2018 Oct;106:1357-1363. doi: 10.1016/j.biopha.2018.07.059. Epub 2018 Jul 23.
5
Activation of the IGF1R pathway potentially mediates acquired resistance to mutant-selective 3rd-generation EGF receptor tyrosine kinase inhibitors in advanced non-small cell lung cancer.胰岛素样生长因子1受体(IGF1R)通路的激活可能介导晚期非小细胞肺癌对突变选择性第三代表皮生长因子受体酪氨酸激酶抑制剂产生获得性耐药。
Oncotarget. 2016 Apr 19;7(16):22005-15. doi: 10.18632/oncotarget.8013.
6
Inhibition of the IGF signaling pathway reverses cisplatin resistance in ovarian cancer cells.抑制 IGF 信号通路可逆转卵巢癌细胞对顺铂的耐药性。
BMC Cancer. 2017 Dec 14;17(1):851. doi: 10.1186/s12885-017-3840-1.
7
miR-223 reverses the resistance of EGFR-TKIs through IGF1R/PI3K/Akt signaling pathway.微小RNA-223通过胰岛素样生长因子1受体/磷脂酰肌醇-3-激酶/蛋白激酶B信号通路逆转表皮生长因子受体酪氨酸激酶抑制剂的耐药性。
Int J Oncol. 2016 May;48(5):1855-67. doi: 10.3892/ijo.2016.3401. Epub 2016 Feb 19.
8
Inhibition of IGF1R signaling abrogates resistance to afatinib (BIBW2992) in EGFR T790M mutant lung cancer cells.抑制IGF1R信号传导可消除EGFR T790M突变肺癌细胞对阿法替尼(BIBW2992)的耐药性。
Mol Carcinog. 2016 May;55(5):991-1001. doi: 10.1002/mc.22342. Epub 2015 Jun 4.
9
IGF-IR signaling in epithelial to mesenchymal transition and targeting IGF-IR therapy: overview and new insights.胰岛素样生长因子-1受体(IGF-IR)信号传导在上皮-间质转化及IGF-IR靶向治疗中的作用:综述与新见解
Mol Cancer. 2017 Jan 30;16(1):6. doi: 10.1186/s12943-016-0576-5.
10
Targeting melanoma with NT157 by blocking Stat3 and IGF1R signaling.通过阻断Stat3和IGF1R信号通路,用NT157靶向治疗黑色素瘤。
Oncogene. 2016 May 19;35(20):2675-80. doi: 10.1038/onc.2015.229. Epub 2015 Jun 29.

引用本文的文献

1
Establishment and characterization of a new human gallbladder cancer cell line, OCUG-2.一种新的人胆囊癌细胞系OCUG-2的建立与鉴定。
World J Exp Med. 2025 Jun 20;15(2):100443. doi: 10.5493/wjem.v15.i2.100443.
2
IGF-1R inhibitors in cancer: A review of available evidence and future outlook.癌症中的胰岛素样生长因子-1受体(IGF-1R)抑制剂:现有证据综述与未来展望
Crit Rev Oncol Hematol. 2025 Jun 15;214:104809. doi: 10.1016/j.critrevonc.2025.104809.
3
[Predictive Value of miRNAs Markers for Advanced Lung Squamous Cell Carcinoma].[微小RNA标志物对晚期肺鳞状细胞癌的预测价值]
Zhongguo Fei Ai Za Zhi. 2025 May 20;28(5):325-333. doi: 10.3779/j.issn.1009-3419.2025.102.16.
4
IGF1R signalling is a guardian of self-tolerance restricting autoantibody production.IGF1R 信号是自身耐受的守护者,限制自身抗体的产生。
Front Immunol. 2022 Aug 29;13:958206. doi: 10.3389/fimmu.2022.958206. eCollection 2022.
5
Astrocytic IGF-1 and IGF-1R Orchestrate Mitophagy in Traumatic Brain Injury via Exosomal miR-let-7e.星形胶质细胞 IGF-1 和 IGF-1R 通过外泌体 miR-let-7e 调控创伤性脑损伤中的自噬。
Oxid Med Cell Longev. 2022 Aug 24;2022:3504279. doi: 10.1155/2022/3504279. eCollection 2022.
6
Noncoding RNA actions through IGFs and IGF binding proteins in cancer.非编码 RNA 通过 IGFs 和 IGF 结合蛋白在癌症中的作用。
Oncogene. 2022 Jun;41(25):3385-3393. doi: 10.1038/s41388-022-02353-3. Epub 2022 May 21.
7
STAT3 activation regulated circ-STAT3.46 promote expression of IGF1R by sponging of miR-139-5p in human colon cancer.STAT3激活调控的circ-STAT3.46通过海绵吸附miR-139-5p促进人结肠癌中IGF1R的表达。
Transl Cancer Res. 2019 Nov;8(7):2593-2601. doi: 10.21037/tcr.2019.10.31.
8
Mechanism of miR-98 inhibiting tumor proliferation and invasion by targeting IGF1R in diabetic patients combined with colon cancer.miR-98通过靶向IGF1R抑制糖尿病合并结肠癌患者肿瘤增殖和侵袭的机制
Oncol Lett. 2020 Aug;20(2):1719-1726. doi: 10.3892/ol.2020.11707. Epub 2020 Jun 9.
9
Insulin-like growth factor receptor signaling in tumorigenesis and drug resistance: a challenge for cancer therapy.胰岛素样生长因子受体信号在肿瘤发生和耐药中的作用:癌症治疗的挑战。
J Hematol Oncol. 2020 Jun 3;13(1):64. doi: 10.1186/s13045-020-00904-3.
10
Expressions of miR-21 and miR-210 in Breast Cancer and Their Predictive Values for Prognosis.miR-21和miR-210在乳腺癌中的表达及其对预后的预测价值
Iran J Public Health. 2020 Jan;49(1):21-29.

本文引用的文献

1
miR-211-5p Suppresses Metastatic Behavior by Targeting SNAI1 in Renal Cancer.miR-211-5p 通过靶向肾癌细胞中的 SNAI1 抑制转移行为。
Mol Cancer Res. 2017 Apr;15(4):448-456. doi: 10.1158/1541-7786.MCR-16-0288. Epub 2017 Jan 5.
2
Snail-Modulated MicroRNA 493 Forms a Negative Feedback Loop with the Insulin-Like Growth Factor 1 Receptor Pathway and Blocks Tumorigenesis.蜗牛调控的微小RNA 493与胰岛素样生长因子1受体途径形成负反馈环并阻断肿瘤发生。
Mol Cell Biol. 2017 Mar 1;37(6). doi: 10.1128/MCB.00510-16. Print 2017 Mar 15.
3
miR-486-5p suppresses prostate cancer metastasis by targeting Snail and regulating epithelial-mesenchymal transition.微小RNA-486-5p通过靶向Snail并调节上皮-间质转化来抑制前列腺癌转移。
Onco Targets Ther. 2016 Nov 8;9:6909-6914. doi: 10.2147/OTT.S117338. eCollection 2016.
4
MiR-132 plays an oncogenic role in laryngeal squamous cell carcinoma by targeting FOXO1 and activating the PI3K/AKT pathway.微小RNA-132通过靶向叉头框蛋白O1并激活磷脂酰肌醇-3-激酶/蛋白激酶B信号通路在喉鳞状细胞癌中发挥致癌作用。
Eur J Pharmacol. 2016 Dec 5;792:1-6. doi: 10.1016/j.ejphar.2016.10.015. Epub 2016 Oct 15.
5
MicroRNA-153 inhibits tumor progression in esophageal squamous cell carcinoma by targeting SNAI1.微小RNA-153通过靶向SNAI1抑制食管鳞状细胞癌的肿瘤进展。
Tumour Biol. 2016 Dec;37:16135–16140. doi: 10.1007/s13277-016-5427-x. Epub 2016 Oct 13.
6
Profiling of downregulated blood-circulating miR-150-5p as a novel tumor marker for cholangiocarcinoma.下调的血液循环miR-150-5p作为胆管癌新型肿瘤标志物的分析
Tumour Biol. 2016 Nov;37(11):15019-15029. doi: 10.1007/s13277-016-5313-6. Epub 2016 Sep 22.
7
MicroRNA-9 regulates the development of knee osteoarthritis through the NF-kappaB1 pathway in chondrocytes.微小RNA-9通过软骨细胞中的核因子κB1途径调节膝骨关节炎的发展。
Medicine (Baltimore). 2016 Sep;95(36):e4315. doi: 10.1097/MD.0000000000004315.
8
MiR-137 and miR-34a directly target Snail and inhibit EMT, invasion and sphere-forming ability of ovarian cancer cells.微小RNA-137和微小RNA-34a直接靶向蜗牛蛋白,并抑制卵巢癌细胞的上皮-间质转化、侵袭和球体形成能力。
J Exp Clin Cancer Res. 2016 Sep 5;35(1):132. doi: 10.1186/s13046-016-0415-y.
9
Tumor suppressor miRNA-204-5p promotes apoptosis by targeting BCL2 in prostate cancer cells.抑癌 miRNA-204-5p 通过靶向前列腺癌细胞中的 BCL2 促进细胞凋亡。
Asian J Surg. 2017 Sep;40(5):396-406. doi: 10.1016/j.asjsur.2016.07.001. Epub 2016 Aug 9.
10
miR-1303 promotes the proliferation of neuroblastoma cell SH-SY5Y by targeting GSK3β and SFRP1.miR-1303 通过靶向 GSK3β 和 SFRP1 促进神经母细胞瘤细胞 SH-SY5Y 的增殖。
Biomed Pharmacother. 2016 Oct;83:508-513. doi: 10.1016/j.biopha.2016.07.010. Epub 2016 Jul 18.

用 microRNAs 靶向癌症中的 IGF1R 通路:我们有多接近?

Targeting IGF1R pathway in cancer with microRNAs: How close are we?

机构信息

a Department of Biotechnology , Indian Institute of Technology, Madras (IIT M) , Chennai , India.

b Department of Human Genetics , College of Biomedical Sciences, Technology & Research, Sri Ramachandra University , Porur, Chennai , India.

出版信息

RNA Biol. 2018 Mar 4;15(3):320-326. doi: 10.1080/15476286.2017.1338240. Epub 2018 Feb 1.

DOI:10.1080/15476286.2017.1338240
PMID:28613101
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5927721/
Abstract

Cancer of the head and neck are the most common cancers in India and account for 30% of all cancers. At molecular level, it could be attributed to the overexpression of growth factors like IGF1-R, EGFR, VEGF-R and deregulation of cell cycle regulators and tumor suppressors. IGF1-R is an emerging target in head and neck cancer treatment, because of its reported role in tumor development, progression and metastasis. IGF1R targeted agents are in advanced stages of clinical development. Nevertheless, these agents suffer from several disadvantages including acquired resistance and toxic side effects. Hence there is a need for developing newer agents targeting not only the receptor but also its downstream signaling. miRNAs are considered as master regulators of gene expression of multiple genes and has been widely reported to be a promising therapeutic strategy. This review discusses the present status of research in both these arenas and emphasizes the role of miRNA as a promising agent for biologic therapy.

摘要

头颈部癌症是印度最常见的癌症,占所有癌症的 30%。在分子水平上,这可能归因于生长因子如 IGF1-R、EGFR、VEGF-R 的过表达和细胞周期调节剂和肿瘤抑制因子的失调。IGF1-R 是头颈部癌症治疗的一个新兴靶点,因为它在肿瘤的发展、进展和转移中发挥作用。IGF1R 靶向药物处于临床开发的后期阶段。然而,这些药物存在多种缺点,包括获得性耐药和毒副作用。因此,需要开发新的药物,不仅针对受体,还针对其下游信号。miRNA 被认为是多个基因的基因表达的主要调控因子,并且已被广泛报道为一种很有前途的治疗策略。本文综述了这两个领域的研究现状,并强调了 miRNA 作为生物治疗有前途的药物的作用。