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The macrophage stimulating protein/Ron pathway as a potential therapeutic target to impede multiple mechanisms involved in breast cancer progression.

Abstract
Macrophage Stimulating Protein (MSP) is the only known ligand for the receptor tyrosine kinase Ron. The MSP/Ron pathway is involved in several important biological processes, including macrophage activity, wound healing, and epithelial cell behavior. A role for MSP/Ron in breast cancer has recently been elucidated, wherein this pathway regulates tumor growth, angiogenesis, and metastasis. Here, we review the recent literature surrounding MSP/Ron function in tumor cells, inflammatory cells, and osteoclasts - cell types that often coexist in breast tumor microenvironments. We discuss the potential implications of MSP/Ron activity occurring concurrently in these cell types on tumor progression and metastasis. Lastly, we outline the potential for targeting MSP/Ron as a novel therapy for breast cancer, and for other cancer types.
AuthorsKelsi L Kretschmann, Henok Eyob, Saundra S Buys, Alana L Welm
JournalCurrent drug targets (Curr Drug Targets) Vol. 11 Issue 9 Pg. 1157-68 (Sep 2010) ISSN: 1873-5592 [Electronic] United Arab Emirates
PMID20545605 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Review)
Chemical References
  • Proto-Oncogene Proteins
  • macrophage stimulating protein
  • Hepatocyte Growth Factor
  • RON protein
  • Receptor Protein-Tyrosine Kinases
Topics
  • Animals
  • Breast Neoplasms (drug therapy, metabolism, physiopathology)
  • Cell Line, Tumor
  • Disease Progression
  • Epithelial Cells (metabolism)
  • Female
  • Hepatocyte Growth Factor (metabolism)
  • Humans
  • Inflammation (physiopathology)
  • Macrophages (physiology)
  • Mice
  • Mice, Transgenic
  • Molecular Targeted Therapy
  • Neoplasms (drug therapy, metabolism)
  • Osteoclasts (metabolism)
  • Proto-Oncogene Proteins (metabolism)
  • Receptor Protein-Tyrosine Kinases (antagonists & inhibitors, metabolism)
  • Signal Transduction
  • Wound Healing

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