Src/FAK-mediated regulation of E-cadherin as a mechanism for controlling collective cell movement Insights from in vivo imaging

Alan Serrels*, Marta Canel, Valerie G. Brunton, Margaret C. Frame

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Recent advances in confocal and multi-photon microscopy, together with fluorescent probe development, have enabled cancer biology studies to go beyond the culture dish and interrogate cancer-associated processes in the complex in vivo environment. Regulation of the tumor suppressor protein E-cadherin plays an important role in cancer development and progression, and may contribute to the decision between 'single cell' and 'collective invasion' in vivo. Mounting evidence from in vitro and in vivo experiments places the two nonreceptor protein tyrosine kinases Src and Focal Adhesion Kinase at the heart of E-cadherin regulation and the crosstalk between integrins and cadherins. Here we discuss recent insights, attained using high-resolution fluorescent in vivo imaging, into the regulation of E-cadherin and collective invasion. We focus on the regulatory crosstalk between the Src/FAK signaling axis and E-cadherin in vivo.

Original languageEnglish
Pages (from-to)360-365
Number of pages6
JournalCell Adhesion and Migration
Volume5
Issue number4
DOIs
Publication statusPublished - 2011

Keywords / Materials (for Non-textual outputs)

  • fluorescent in vivo imaging
  • HUMAN-COLON CARCINOMA
  • METASTASIS
  • Src
  • E-cadherin
  • EMT
  • SRC
  • FOCAL ADHESION KINASE
  • ACTIVATION
  • TUMOR PROGRESSION
  • FAK
  • INVASION
  • EPITHELIAL-MESENCHYMAL TRANSITION
  • MIGRATION
  • CANCER CELLS

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