期刊文献+

Roles of Rap1 signaling in tumor cell migration and invasion 被引量:10

Roles of Rap1 signaling in tumor cell migration and invasion
下载PDF
导出
摘要 Ras-associated protein-1(Rap1), a small GTPase in the Ras-related protein family, is an important regulator of basic cellular functions(e.g., formation and control of cell adhesions and junctions), cellular migration, and polarization. Through its interaction with other proteins, Rap1 plays many roles during cell invasion and metastasis in different cancers. The basic function of Rap1 is straightforward; it acts as a switch during cellular signaling transduction and regulated by its binding to either guanosine triphosphate(GTP) or guanosine diphosphate(GDP). However, its remarkably diverse function is rendered by its interplay with a large number of distinct Rap guanine nucleotide exchange factors and Rap GTPase activating proteins. This review summarizes the mechanisms by which Rap1 signaling can regulate cell invasion and metastasis, focusing on its roles in integrin and cadherin regulation, Rho GTPase control, and matrix metalloproteinase expression. Ras-associated protein-1 (Rapl), a small GTPase in the Ras-related protein family, is an important regulator of basic cellular functions (e.g., formation and control of cell adhesions and junctions), cellular migration, and polarization. Through its interaction with other proteins, Rapl plays many roles during cell invasion and metastasis in different cancers. The basic function of Rapl is straightforward; it acts as a switch during cellular signaling transduction and regulated by its binding to either guanosine triphosphate (GTP) or guanosine diphosphate (GDP). However, its remarkably diverse function is rendered by its interplay with a large number of distinct Rap guanine nucleotide exchange factors and Rap GTPase activating proteins. This review summarizes the mechanisms by which Rap 1 signaling can regulate cell invasion and metastasis, focusing on its roles in integrin and cadherin regulation, Rho GTPase control, and matrix metalloproteinase expression.
出处 《Cancer Biology & Medicine》 SCIE CAS CSCD 2017年第1期90-99,共10页 癌症生物学与医学(英文版)
基金 supported by grants from the National Natural Science Foundation of China(Grant No.31271504 and 31471310) the Shenzhen Science and Technology Innovation Committee,China(Grant No.JCYJ2013040 1144744187)
  • 相关文献

同被引文献65

引证文献10

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部