基质硬化通过口周蛋白-整联蛋白机械传导途径促进癌症的集体侵袭。

IF 4.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Matrix Biology Pub Date : 2023-08-01 DOI:10.1016/j.matbio.2023.05.006
Tiantian Wu , Shanshan Xiong , Mimi Chen , Bjorn T. Tam , Wei Chen , Ke Dong , Zhenling Ma , Zhe Wang , Gaoliang Ouyang
{"title":"基质硬化通过口周蛋白-整联蛋白机械传导途径促进癌症的集体侵袭。","authors":"Tiantian Wu ,&nbsp;Shanshan Xiong ,&nbsp;Mimi Chen ,&nbsp;Bjorn T. Tam ,&nbsp;Wei Chen ,&nbsp;Ke Dong ,&nbsp;Zhenling Ma ,&nbsp;Zhe Wang ,&nbsp;Gaoliang Ouyang","doi":"10.1016/j.matbio.2023.05.006","DOIUrl":null,"url":null,"abstract":"<div><p>Matrix rigidity is a critical contributor to tumor progression; however, whether and how matrix stiffness modulates the collective invasion of tumor cells remain unknown. Here we demonstrate that increased matrix stiffness activates YAP to promote the secretion of periostin (POSTN) in cancer-associated fibroblasts, which in turn augments the matrix rigidity of mammary glands and breast tumor tissues by facilitating collagen crosslinking. Moreover, decreased tissue stiffening resulted from the POSTN deficiency impairs peritoneal metastatic potential of orthotopic breast tumors. Increased matrix stiffness also promotes three-dimensional (3D) collective breast tumor cell invasion via multicellular cytoskeleton remodeling. POSTN triggers the integrin/FAK/ERK/Cdc42/Rac1 mechanotransduction pathway during 3D collective invasion of breast tumor. Clinically, high POSTN expression correlates with high collagen levels in breast tumors and cooperatively determines the metastatic recurrence potential in breast cancer patients. Collectively, these findings indicate that matrix rigidity promotes 3D collective invasion of breast tumor cells via the YAP-POSTN-integrin mechanotransduction signaling.</p></div>","PeriodicalId":49851,"journal":{"name":"Matrix Biology","volume":"121 ","pages":"Pages 22-40"},"PeriodicalIF":4.5000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Matrix stiffening facilitates the collective invasion of breast cancer through the periostin-integrin mechanotransduction pathway\",\"authors\":\"Tiantian Wu ,&nbsp;Shanshan Xiong ,&nbsp;Mimi Chen ,&nbsp;Bjorn T. Tam ,&nbsp;Wei Chen ,&nbsp;Ke Dong ,&nbsp;Zhenling Ma ,&nbsp;Zhe Wang ,&nbsp;Gaoliang Ouyang\",\"doi\":\"10.1016/j.matbio.2023.05.006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Matrix rigidity is a critical contributor to tumor progression; however, whether and how matrix stiffness modulates the collective invasion of tumor cells remain unknown. Here we demonstrate that increased matrix stiffness activates YAP to promote the secretion of periostin (POSTN) in cancer-associated fibroblasts, which in turn augments the matrix rigidity of mammary glands and breast tumor tissues by facilitating collagen crosslinking. Moreover, decreased tissue stiffening resulted from the POSTN deficiency impairs peritoneal metastatic potential of orthotopic breast tumors. Increased matrix stiffness also promotes three-dimensional (3D) collective breast tumor cell invasion via multicellular cytoskeleton remodeling. POSTN triggers the integrin/FAK/ERK/Cdc42/Rac1 mechanotransduction pathway during 3D collective invasion of breast tumor. Clinically, high POSTN expression correlates with high collagen levels in breast tumors and cooperatively determines the metastatic recurrence potential in breast cancer patients. Collectively, these findings indicate that matrix rigidity promotes 3D collective invasion of breast tumor cells via the YAP-POSTN-integrin mechanotransduction signaling.</p></div>\",\"PeriodicalId\":49851,\"journal\":{\"name\":\"Matrix Biology\",\"volume\":\"121 \",\"pages\":\"Pages 22-40\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2023-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Matrix Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0945053X23000690\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Matrix Biology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0945053X23000690","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

基质刚性是肿瘤进展的关键因素;然而,基质硬度是否以及如何调节肿瘤细胞的集体侵袭仍然未知。在这里,我们证明,增加的基质硬度激活YAP,以促进癌症相关成纤维细胞中周缘素(POSTN)的分泌,这反过来又通过促进胶原蛋白交联来增强乳腺和乳腺肿瘤组织的基质硬度。此外,POSTN缺乏导致的组织硬化减少削弱了原位乳腺肿瘤的腹膜转移潜力。增加的基质硬度也通过多细胞骨架重塑促进三维(3D)集体乳腺肿瘤细胞侵袭。POSTN在乳腺肿瘤的3D集体侵袭过程中触发整合素/FAK/ERK/Cdc42/Rac1机械转导途径。临床上,高POSTN表达与乳腺肿瘤中的高胶原水平相关,并共同决定了乳腺癌症患者转移复发的可能性。总之,这些发现表明,基质刚性通过YAP-POSTN整合素机械转导信号促进乳腺肿瘤细胞的3D集体侵袭。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Matrix stiffening facilitates the collective invasion of breast cancer through the periostin-integrin mechanotransduction pathway

Matrix rigidity is a critical contributor to tumor progression; however, whether and how matrix stiffness modulates the collective invasion of tumor cells remain unknown. Here we demonstrate that increased matrix stiffness activates YAP to promote the secretion of periostin (POSTN) in cancer-associated fibroblasts, which in turn augments the matrix rigidity of mammary glands and breast tumor tissues by facilitating collagen crosslinking. Moreover, decreased tissue stiffening resulted from the POSTN deficiency impairs peritoneal metastatic potential of orthotopic breast tumors. Increased matrix stiffness also promotes three-dimensional (3D) collective breast tumor cell invasion via multicellular cytoskeleton remodeling. POSTN triggers the integrin/FAK/ERK/Cdc42/Rac1 mechanotransduction pathway during 3D collective invasion of breast tumor. Clinically, high POSTN expression correlates with high collagen levels in breast tumors and cooperatively determines the metastatic recurrence potential in breast cancer patients. Collectively, these findings indicate that matrix rigidity promotes 3D collective invasion of breast tumor cells via the YAP-POSTN-integrin mechanotransduction signaling.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Matrix Biology
Matrix Biology 生物-生化与分子生物学
CiteScore
11.40
自引率
4.30%
发文量
77
审稿时长
45 days
期刊介绍: Matrix Biology (established in 1980 as Collagen and Related Research) is a cutting-edge journal that is devoted to publishing the latest results in matrix biology research. We welcome articles that reside at the nexus of understanding the cellular and molecular pathophysiology of the extracellular matrix. Matrix Biology focusses on solving elusive questions, opening new avenues of thought and discovery, and challenging longstanding biological paradigms.
期刊最新文献
Identification of CD44 as a key engager to hyaluronic acid-rich extracellular matrices for cell traction force generation and tumor invasion in 3D Remodeling of the extracellular matrix by serine proteases as a prerequisite for cancer initiation and progression The epidermal integrin-mediated secretome regulates the skin microenvironment during tumorigenesis and repair Extracellular matrix integrity regulates GABAergic plasticity in the hippocampus Effects of hydrostatic pressure, osmotic pressure, and confinement on extracellular matrix associated responses in the nucleus pulposus cells ex vivo
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1