机械转化
骨膜炎
整合素
细胞外基质
乳腺癌
癌症研究
细胞生物学
转移
静脉注射
生物
医学
病理
化学
内科学
癌症
受体
作者
Tiantian Wu,Shanshan Xiong,Mimi Chen,Bjorn T. Tam,Wei Chen,Ke Dong,Zhenling Ma,Zhe Wang,Gaoliang Ouyang
出处
期刊:Matrix Biology
[Elsevier BV]
日期:2023-05-23
卷期号:121: 22-40
被引量:13
标识
DOI:10.1016/j.matbio.2023.05.006
摘要
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.
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