TY - JOUR
T1 - RON, a tyrosine kinase receptor involved in tumor progression and metastasis
AU - Camp, E. Ramsay
AU - Liu, Wenbiao
AU - Fan, Fan
AU - Yang, Anthony
AU - Somcio, Ray
AU - Ellis, Lee M.
PY - 2005/4
Y1 - 2005/4
N2 - Tyrosine kinase receptors mediate many critical cellular functions that contribute to tumor progression and metastasis and thus are potential targets for molecular-based cancer therapy. As has been found for many receptor tyrosine kinases, RON (recepteur d'origine nantais) and its ligand, macrophage- stimulating protein, have recently been implicated in the progression and metastasis of tumors. In in vitro experiments using colon and breast cancer cell lines, overexpression of RON led to increased invasion and migration of cancer cells and prevented apoptosis and anoikis. In addition, transgenic mice engineered to overexpress RON in the lung epithelium developed multiple pulmonary tumors, suggesting a role for RON in tumorigenesis. In human cancer specimens, increased RON expression has been demonstrated in colon, breast, ovarian, and lung tumors. Therefore, therapies designed to inhibit RON activation may hinder critical tumor survival mechanisms and play a role in the treatment of advanced disease.
AB - Tyrosine kinase receptors mediate many critical cellular functions that contribute to tumor progression and metastasis and thus are potential targets for molecular-based cancer therapy. As has been found for many receptor tyrosine kinases, RON (recepteur d'origine nantais) and its ligand, macrophage- stimulating protein, have recently been implicated in the progression and metastasis of tumors. In in vitro experiments using colon and breast cancer cell lines, overexpression of RON led to increased invasion and migration of cancer cells and prevented apoptosis and anoikis. In addition, transgenic mice engineered to overexpress RON in the lung epithelium developed multiple pulmonary tumors, suggesting a role for RON in tumorigenesis. In human cancer specimens, increased RON expression has been demonstrated in colon, breast, ovarian, and lung tumors. Therefore, therapies designed to inhibit RON activation may hinder critical tumor survival mechanisms and play a role in the treatment of advanced disease.
KW - Cancer
KW - Macrophage-stimulating protein
KW - RON
KW - Tyrosine kinase receptor
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U2 - 10.1245/ASO.2005.08.013
DO - 10.1245/ASO.2005.08.013
M3 - Review article
C2 - 15827676
AN - SCOPUS:18144422402
SN - 1068-9265
VL - 12
SP - 273
EP - 281
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 4
ER -