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Roles of Rap1 signaling in tumor cell migration and invasion 被引量:10
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作者 yi-lei zhang Ruo-Chen Wang +2 位作者 Ken Cheng Brian Z.Ring Li Su 《Cancer Biology & Medicine》 SCIE CAS CSCD 2017年第1期90-99,共10页
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 migr... 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. 展开更多
关键词 TUMOR METASTASIS Rapl RapGEFs RapGAPs
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