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Ephs and ephrins in cancer: ephrin-A1 signalling.

Abstract
Ephrin-A1 and its primary receptor, EphA2, are involved in numerous physiological processes and have been intensely studied for their roles in malignancy. Ephrin-Eph signalling is complex on its own and is also cell-type dependent, making elucidation of the exact role of ephrin-A1 in neoplasia challenging. Multiple oncogenic signalling pathways, such as MAP/ERK and PI3K are affected by ephrin-A1, and in some cases evidence suggests the promotion of a specific pathway in one cell or cancer type and inhibition of the same pathway in another type of cell or cancer. Ephrin-A1 also plays an integral role in angiogenesis and tumor neovascularization. Until recently, studies investigating ephrins focused on the ligands as GPI-anchored proteins that required membrane anchoring or artificial clustering for Eph receptor activation. However, recent studies have demonstrated a functional role for soluble, monomeric ephrin-A1. This review will focus on various forms of ephrin-A1-specific signalling in human malignancy.
AuthorsAmanda Beauchamp, Waldemar Debinski
JournalSeminars in cell & developmental biology (Semin Cell Dev Biol) Vol. 23 Issue 1 Pg. 109-15 (Feb 2012) ISSN: 1096-3634 [Electronic] England
PMID22040911 (Publication Type: Journal Article, Review)
CopyrightCopyright © 2011 Elsevier Ltd. All rights reserved.
Chemical References
  • Ephrin-A1
  • Receptor, EphA2
  • rho GTP-Binding Proteins
Topics
  • Animals
  • Cell Physiological Phenomena
  • Cytoskeleton (metabolism)
  • Endothelial Cells (metabolism)
  • Ephrin-A1 (chemistry, metabolism, physiology)
  • Humans
  • Neoplasms (blood supply, metabolism, pathology)
  • Neovascularization, Pathologic (metabolism)
  • Protein Structure, Tertiary
  • Receptor, EphA2 (metabolism)
  • Signal Transduction
  • rho GTP-Binding Proteins (metabolism)

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