ABSTRACT:
BACKGROUND:
Dovitinib is a receptor tyrosine kinase (RTK) inhibitor targeting vascular endothelial
growth factor receptors, fibroblast growth factor receptors and
platelet-derived growth factor receptor beta. Dovitinib is currently in
clinical trials for the treatment of hepatocellular carcinoma (HCC).
METHOD:
In
this study, we used five HCC cell lines and five endothelial cell lines to
validate molecular and cellular targets of dovitinib.
RESULTS:
Tumor
growth and pulmonary metastasis were significantly suppressed in an orthotopic
HCC model. Immunoblotting revealed that among known dovitinib targets, only
PDGFR-beta was expressed in two HCC cell lines, while four of five endothelial
lines expressed PDGFR-beta, FGFR-1, and VEGFR-2. Dovitinib inhibited
endothelial cell proliferation and motility at 0.04 mumol/L, a
pharmacologically relevant concentration; it was unable to inhibit the
proliferation or motility of HCC cells at the same concentration.
Immunohistochemical analyses showed that dovitinib significantly decreased the
microvessel density of xenograft tumors, inhibiting proliferation and inducing
apoptosis in HCC cells.
CONCLUSION:
Our
findings indicate that dovitinib inhibits HCC growth and metastasis
preferentially through an antiangiogenic mechanism, not through direct
targeting of HCC cells.
Source:
Dovitinib preferentially targets endothelial cells rather than cancer
cells for the inhibition of hepatocellular carcinoma growth and metastasis.
Chen ZY, Shi M, Peng LX, Wei W, Li XJ, Guo ZX, Li SH, Zhong C, Qian CN, Guo RP
(guorp@sysucc.org.cn). J Transl Med.
2012 Dec 10;10(1):245.
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