Structural Features of Glypicans and their Impact on Wnt Signaling in Cancer.

Proteoglycan research Pub Date : 2025-04-01 Epub Date: 2025-05-13 DOI:10.1002/pgr2.70029
Hsi-En Tsao, Mitchell Ho
{"title":"Structural Features of Glypicans and their Impact on Wnt Signaling in Cancer.","authors":"Hsi-En Tsao, Mitchell Ho","doi":"10.1002/pgr2.70029","DOIUrl":null,"url":null,"abstract":"<p><p>Glypicans (GPCs) are a family of cell surface proteoglycans involved in multiple signaling pathways that regulate cell fate and proliferation. They share a characteristic structure composed of a core protein with two or more heparan sulfate chains and a glycosyl-phosphatidylinositol anchor that attaches them to the cell membrane. Aberrant expression of certain glypicans such as GPC1, GPC2, and GPC3 has been found in multiple types of cancer and causes the dysregulation of Wnt, hedgehog, and other signaling pathways, making them emerging targets for cancer immunotherapy. The molecular mechanism by which glypicans interact with signaling factors will provide insights for the development of cancer therapeutics. However, the structural complexes of human glypicans with Wnt and other key signaling factors remain unsolved. In this brief review, we analyze the current protein structural evidence for glypicans, with an emphasis on their interaction with Wnt, in an effort to provide insights to understand the molecular mechanisms by which glypicans play positive or negative roles in Wnt signaling in cancer and to discuss their translational potentials.</p>","PeriodicalId":74585,"journal":{"name":"Proteoglycan research","volume":"3 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12101617/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proteoglycan research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/pgr2.70029","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/13 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Glypicans (GPCs) are a family of cell surface proteoglycans involved in multiple signaling pathways that regulate cell fate and proliferation. They share a characteristic structure composed of a core protein with two or more heparan sulfate chains and a glycosyl-phosphatidylinositol anchor that attaches them to the cell membrane. Aberrant expression of certain glypicans such as GPC1, GPC2, and GPC3 has been found in multiple types of cancer and causes the dysregulation of Wnt, hedgehog, and other signaling pathways, making them emerging targets for cancer immunotherapy. The molecular mechanism by which glypicans interact with signaling factors will provide insights for the development of cancer therapeutics. However, the structural complexes of human glypicans with Wnt and other key signaling factors remain unsolved. In this brief review, we analyze the current protein structural evidence for glypicans, with an emphasis on their interaction with Wnt, in an effort to provide insights to understand the molecular mechanisms by which glypicans play positive or negative roles in Wnt signaling in cancer and to discuss their translational potentials.

Glypicans的结构特征及其对癌症中Wnt信号传导的影响。
Glypicans (GPCs)是一个细胞表面蛋白聚糖家族,参与调节细胞命运和增殖的多种信号通路。它们具有一个具有两个或更多硫酸肝素链的核心蛋白和一个将它们附着在细胞膜上的糖基磷脂酰肌醇锚点组成的特征结构。某些glypicans如GPC1、GPC2和GPC3的异常表达已在多种类型的癌症中被发现,并导致Wnt、hedgehog等信号通路的失调,使其成为癌症免疫治疗的新靶点。glypicans与信号因子相互作用的分子机制将为癌症治疗的发展提供见解。然而,人类glypicans与Wnt和其他关键信号因子的结构复合物仍未得到解决。在这篇简短的综述中,我们分析了目前关于glypicans的蛋白质结构证据,重点分析了它们与Wnt的相互作用,努力为理解glypicans在癌症中Wnt信号传导中发挥积极或消极作用的分子机制提供见解,并讨论了它们的翻译潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信