Eph as a target in inflammation.

Abstract

Evidence to show that the Eph/ephrin system is involved in inflammation induced by infection, injury, inflammatory diseases, and atherosclerosis has been increased. Although the roles of the Eph/ephrin system in both neural and vascular development as well as cell motility are well documented, its involvement in inflammatory processes has not yet been elucidated in detail. Moreover, the soluble form of artificially oligomerized or dimerized Fc-fused ephrin-A1 has been widely used in in vitro and/or in vivo studies to activate the EphA receptors, whereas its physiological functions as a membrane-anchored protein remain largely unknown. Recent studies using clinical samples reported that the overexpression of Ephs and ephrins in some tumors such as hepatocellular carcinoma positively correlated with both malignancy of tumors and the poor prognosis of cancer patients. However, the molecular mechanisms underlying malignancy of tumors are not fully understood. The author herein summarizes the molecular mechanisms of the Eph/ephrin system involved in the immune system and inflammatory processes. Especially, the author focuses on inflammation-induced physiological changes in vascular endothelial cells leading to vascular hyper-permeability and described them in this review. The author also introduces those that contribute to ephrin-A1-mediated lung metastasis.

• Authors: Katsuaki Ieguchi
• Journal: Endocrine, metabolic & immune disorders drug targets (Endocr Metab Immune Disord Drug Targets) Vol. 15 Issue 2 Pg. 119-28 ( 2015) ISSN: 2212-3873 [Electronic] United Arab Emirates
• PMID: 25772170 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)

Chemical References

• Anti-Inflammatory Agents
• Antineoplastic Agents
• Ephrins
• Inflammation Mediators
• Receptors, Eph Family

Topics

• Animals
• Anti-Inflammatory Agents (therapeutic use)
• Antineoplastic Agents (therapeutic use)
• Capillary Permeability
• Drug Design
• Endothelial Cells (metabolism)
• Ephrins (antagonists & inhibitors, metabolism)
• Humans
• Inflammation (drug therapy, immunology, metabolism)
• Inflammation Mediators (antagonists & inhibitors, metabolism)
• Molecular Targeted Therapy
• Neoplasm Metastasis
• Neoplasms (drug therapy, metabolism, pathology)
• Receptors, Eph Family (antagonists & inhibitors, metabolism)
• Signal Transduction (drug effects)