Targeting SHP2 with an Active Site Inhibitor Blocks Signaling and Breast Cancer Cell Phenotypes
Author:
Affiliation:
1. One Medical Center Drive, Department of Biochemistry and Molecular Medicine, School of Medicine, West Virginia University, P.O. Box 9142, Morgantown, West Virginia 26506, United States
Funder
National Cancer Institute
Publisher
American Chemical Society (ACS)
Subject
Pharmaceutical Science,Drug Discovery,Molecular Biology,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsbiomedchemau.3c00024
Reference38 articles.
1. Concomitant activation of the PI3K-Akt and the Ras-ERK signaling pathways is essential for transformation by the V-SEA tyrosine kinase oncogene
2. Molecular Mechanism for a Role of SHP2 in Epidermal Growth Factor Receptor Signaling
3. The phosphotyrosine phosphatase SHP2 is a critical mediator of transformation induced by the oncogenic fibroblast growth factor receptor 3
4. Modulation of α-catenin Tyr phosphorylation by SHP2 positively effects cell transformation induced by the constitutively active FGFR3
5. Hepatocyte growth factor (HGF) signals through SHP2 to regulate primary mouse myoblast proliferation
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Discovery of novel substituted pyridine carboxamide derivatives as potent allosteric SHP2 inhibitors;European Journal of Medicinal Chemistry;2024-09
2. Discovery of Novel Allosteric SHP2 Inhibitor Using Pharmacophore-Based Virtual Screening, Molecular Docking, Molecular Dynamics Simulation, and Principal Component Analysis;Pharmaceuticals;2024-07-12
3. SHP2–EGFR States in Dephosphorylation Can Inform Selective SHP2 Inhibitors, Dampening RasGAP Action;The Journal of Physical Chemistry B;2024-05-15
4. Design, Synthesis, Antitumor Activity Evaluation, and Molecular Dynamics Simulation of Some 2-Aminopyrazine Derivatives;Current Computer-Aided Drug Design;2024-03-12
5. Discovery of Novel Substituted Pyridine Carboxamide Derivatives as Potent and Selective Shp2 Allosteric Inhibitors;2024
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3