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Abstract
<p class="first" id="d19532169e104">The aim of the study described here was to investigate
whether ultrasound-mediated
microbubble destruction (UTMD) of targeted microbubbles conjugated with an anti-vascular
endothelial growth factor receptor 2 (anti-VEGFR2) antibody can enhance the therapeutic
effect of doxorubicin (DOX) on a mouse hepatocellular carcinoma (HCC) model bearing
HEP-G2-RFP tumors. The growth of liver tumors in mice was inhibited by using Visistar
VEGFR2 plus ultrasound irradiation and by DOX alone. DOX plus UTMD had an inhibitory
effect on tumor growth beginning on the seventh day of treatment, while Visistar VEGFR2
alone and DOX alone had inhibitory effects beginning on the 11th day. DOX + UTMD significantly
decreased tumor volume and tumor weight compared with DOX alone (p < 0.05) and
Visistar
VEGFR2 alone (p < 0.05). Compared with DOX alone and Visistar VEGFR2 alone, DOX + UTMD
had the highest inhibitory effect on tumor angiogenesis and the highest apoptosis
index. UTMD-targeted microbubbles can significantly enhance the antitumor effect of
DOX on a mouse HCC model, inhibit angiogenesis and induce apoptosis in tumor cells.
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