• 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

胰岛素样生长因子和胰岛素受体信号传导中的Grb10蛋白(综述)。

Grb10 proteins in insulin-like growth factor and insulin receptor signaling (review).

作者信息

Morrione A

机构信息

Kimmel Cancer Center, Thomas Jefferson University, 606 Bluemle Life Sciences Building, Philadelphia, PA 19107-5541, USA.

出版信息

Int J Mol Med. 2000 Feb;5(2):151-4. doi: 10.3892/ijmm.5.2.151.

DOI:10.3892/ijmm.5.2.151
PMID:10639593
Abstract

The adapter protein Grb10 belongs to a superfamily of related proteins that include Grb7, Grb14 and the Caenorhabtidis elegans Mig10. The available data on Grb10 proteins suggest a role of these adapters in signaling downstream of several receptor tyrosine kinases. In the present review the focus is on the interaction between Grb10 proteins and the insulin-like growth factor receptor/insulin receptor, and the role of Grb10 in IGF-I/insulin-induced mitogenesis is discussed, considering that the data available are also partially discordant.

摘要

衔接蛋白Grb10属于一个相关蛋白超家族,该超家族包括Grb7、Grb14和秀丽隐杆线虫Mig10。关于Grb10蛋白的现有数据表明,这些衔接蛋白在几种受体酪氨酸激酶的下游信号传导中发挥作用。在本综述中,重点是Grb10蛋白与胰岛素样生长因子受体/胰岛素受体之间的相互作用,并讨论了Grb10在IGF-I/胰岛素诱导的有丝分裂中的作用,鉴于现有数据也存在部分不一致。

相似文献

1
Grb10 proteins in insulin-like growth factor and insulin receptor signaling (review).胰岛素样生长因子和胰岛素受体信号传导中的Grb10蛋白(综述)。
Int J Mol Med. 2000 Feb;5(2):151-4. doi: 10.3892/ijmm.5.2.151.
2
Grb10 adapter protein as regulator of insulin-like growth factor receptor signaling.Grb10衔接蛋白作为胰岛素样生长因子受体信号传导的调节因子。
J Cell Physiol. 2003 Dec;197(3):307-11. doi: 10.1002/jcp.10363.
3
Grb10 exceeding the boundaries of a common signaling adapter.Grb10超出了常见信号转导衔接蛋白的范畴。
Front Biosci. 2004 Jan 1;9:603-18. doi: 10.2741/1227.
4
Grb10, a positive, stimulatory signaling adapter in platelet-derived growth factor BB-, insulin-like growth factor I-, and insulin-mediated mitogenesis.Grb10,一种在血小板衍生生长因子BB、胰岛素样生长因子I和胰岛素介导的有丝分裂中起正向刺激信号作用的衔接蛋白。
Mol Cell Biol. 1999 Sep;19(9):6217-28. doi: 10.1128/MCB.19.9.6217.
5
The adapter protein GRB10 is an endogenous negative regulator of insulin-like growth factor signaling.衔接蛋白GRB10是胰岛素样生长因子信号通路的内源性负调节因子。
Endocrinology. 2005 Oct;146(10):4399-409. doi: 10.1210/en.2005-0150. Epub 2005 Jul 21.
6
Grb10 interacts differentially with the insulin receptor, insulin-like growth factor I receptor, and epidermal growth factor receptor via the Grb10 Src homology 2 (SH2) domain and a second novel domain located between the pleckstrin homology and SH2 domains.Grb10通过Grb10的Src同源2(SH2)结构域以及位于普列克底物蛋白同源结构域和SH2结构域之间的第二个新结构域,与胰岛素受体、胰岛素样生长因子I受体和表皮生长因子受体发生不同的相互作用。
J Biol Chem. 1998 Mar 20;273(12):6860-7. doi: 10.1074/jbc.273.12.6860.
7
Regulation of insulin and type 1 insulin-like growth factor signaling and action by the Grb10/14 and SH2B1/B2 adaptor proteins.Grb10/14 和 SH2B1/B2 衔接蛋白对胰岛素和 1 型胰岛素样生长因子信号转导和作用的调节。
FEBS J. 2013 Feb;280(3):794-816. doi: 10.1111/febs.12080. Epub 2013 Jan 2.
8
The Grb10/Nedd4 complex regulates ligand-induced ubiquitination and stability of the insulin-like growth factor I receptor.Grb10/Nedd4复合物调节配体诱导的胰岛素样生长因子I受体的泛素化和稳定性。
Mol Cell Biol. 2003 May;23(9):3363-72. doi: 10.1128/MCB.23.9.3363-3372.2003.
9
Interaction of a GRB-IR splice variant (a human GRB10 homolog) with the insulin and insulin-like growth factor I receptors. Evidence for a role in mitogenic signaling.一种GRB-IR剪接变体(人类GRB10同源物)与胰岛素及胰岛素样生长因子I受体的相互作用。有丝分裂信号传导中作用的证据。
J Biol Chem. 1996 Sep 13;271(37):22506-13. doi: 10.1074/jbc.271.37.22506.
10
Grb10: more than a simple adaptor protein.Grb10:不止是一种简单的衔接蛋白。
Front Biosci. 2004 Jan 1;9:387-403. doi: 10.2741/1226.

引用本文的文献

1
No evidence that human GIGYF2 interacts with GRB10: implications for human disease.没有证据表明人类GIGYF2与GRB10相互作用:对人类疾病的启示。
Life Sci Alliance. 2025 Jun 16;8(9). doi: 10.26508/lsa.202503334. Print 2025 Sep.
2
Motif-guided identification of KRAS-interacting proteins.基于模体的 KRAS 相互作用蛋白鉴定。
BMC Biol. 2024 Nov 19;22(1):264. doi: 10.1186/s12915-024-02067-w.
3
CircRNAs as New Therapeutic Entities and Tools for Target Identification in Acute Myeloid Leukemia.环状 RNA 作为急性髓系白血病新的治疗靶点和工具。
Cancer Genomics Proteomics. 2024 Mar-Apr;21(2):118-136. doi: 10.21873/cgp.20434.
4
JASS: command line and web interface for the joint analysis of GWAS results.JASS:用于全基因组关联研究(GWAS)结果联合分析的命令行和网络界面。
NAR Genom Bioinform. 2020 Mar;2(1):lqaa003. doi: 10.1093/nargab/lqaa003. Epub 2020 Jan 24.
5
Insulin Receptor Plasma Membrane Levels Increased by the Progesterone Receptor Membrane Component 1.胰岛素受体的质膜水平通过孕激素受体膜组份 1 增加。
Mol Pharmacol. 2018 Jul;94(1):665-673. doi: 10.1124/mol.117.110510. Epub 2018 Apr 19.
6
Grb7 and Hax1 may colocalize partially to mitochondria in EGF-treated SKBR3 cells and their interaction can affect Caspase3 cleavage of Hax1.在经表皮生长因子(EGF)处理的SKBR3细胞中,Grb7和Hax1可能部分共定位于线粒体,且它们的相互作用会影响Hax1的半胱天冬酶3切割。
J Mol Recognit. 2016 Jul;29(7):318-33. doi: 10.1002/jmr.2533. Epub 2016 Feb 12.
7
Ligand-mediated endocytosis and trafficking of the insulin-like growth factor receptor I and insulin receptor modulate receptor function.配体介导的内吞作用以及胰岛素样生长因子受体I和胰岛素受体的运输调节受体功能。
Front Endocrinol (Lausanne). 2014 Dec 17;5:220. doi: 10.3389/fendo.2014.00220. eCollection 2014.
8
Systemic Sclerosis is a Complex Disease Associated Mainly with Immune Regulatory and Inflammatory Genes.系统性硬化症是一种主要与免疫调节和炎症基因相关的复杂疾病。
Open Rheumatol J. 2014 Sep 29;8:29-42. doi: 10.2174/1874312901408010029. eCollection 2014.
9
GRB10 gene and type 2 diabetes in Whites.GRB10基因与白人中的2型糖尿病
J Intern Med. 2010 Jan;267(1):132-3. doi: 10.1111/j.1365-2796.2009.02089.x. Epub 2009 Oct 9.
10
Tyrosine phosphorylation of growth factor receptor-bound protein-7 by focal adhesion kinase in the regulation of cell migration, proliferation, and tumorigenesis.粘着斑激酶介导的生长因子受体结合蛋白7的酪氨酸磷酸化在细胞迁移、增殖及肿瘤发生调控中的作用
J Biol Chem. 2009 Jul 24;284(30):20215-26. doi: 10.1074/jbc.M109.018259. Epub 2009 May 27.