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.
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Authors | Amanda Beauchamp, Waldemar Debinski |
Journal | Seminars in cell & developmental biology
(Semin Cell Dev Biol)
Vol. 23
Issue 1
Pg. 109-15
(Feb 2012)
ISSN: 1096-3634 [Electronic] England |
PMID | 22040911
(Publication Type: Journal Article, Review)
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Copyright | Copyright © 2011 Elsevier Ltd. All rights reserved. |
Chemical References |
- Ephrin-A1
- Receptor, EphA2
- rho GTP-Binding Proteins
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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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