Roles of Rap1 signaling in tumor cell migration and invasion

Yi Lei Zhang, Ruo Chen Wang, Ken Cheng, Brian Z. Ring, Li Su

Research output: Contribution to journalReview articlepeer-review

133 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)90-99
Number of pages10
JournalCancer Biology and Medicine
Volume14
Issue number1
DOIs
StatePublished - Mar 1 2017

Keywords

  • Metastasis
  • Rap1
  • RapGAPs
  • RapGEFs
  • Tumor

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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