Combination Therapy of Transcatheter Arterial Chemoembolization and Arterial Administration of Antiangiogenesis on VX2 Liver Tumor

被引:28
作者
Deng, Gang [1 ]
Zhao, Deng-Ling [1 ]
Li, Guang-Chao [1 ]
Yu, Hui [1 ]
Teng, Gao-Jun [1 ]
机构
[1] Southeast Univ, Jiangsu Key Lab Mol Imaging & Funct Imaging, Dept Radiol, Zhongda Hosp,Sch Med, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
Liver tumor; Embolization; Arterial; Angiogenesis; Immunohistology; CT; Perfusion; ENDOTHELIAL GROWTH-FACTOR; RECOMBINANT HUMAN ENDOSTATIN; HEPATOCELLULAR-CARCINOMA; FUNCTIONAL-CT; BLOOD-FLOW; ANGIOGENESIS; EMBOLIZATION; PERFUSION; CANCER; LIPIODOL;
D O I
10.1007/s00270-011-0179-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose This study was designed to evaluate the antitumorigenic efficiency of Endostar (an antiangiogenic agent) arterially administrated combined with transcatheter arterial chemoembolization (TACE) on liver tumor, and validation of perfusion CT for quantitative measurements of the results. Experimental Design Thirty rabbits bearing VX2 liver tumors were randomly and equally distributed into three groups. One of the following treatment protocols was performed in each group: 1) group 1 was treated with TACE and simultaneously arterially administrated Endostar; 2) group 2 with TACE alone, and 3) a control group that had saline injected through hepatic artery. Routine CT scan was performed before treatment, and perfusion CT imaging was performed 2 weeks after treatment. Immunohistochemical biomarkers of microvascular density (MVD) and the expression of vascular endothelial growth factor (VEGF) were measured for assessments of angiogenesis. Results We observed a statistically significant reduction from the control in the volume, growth rate, and size of the tumor 2 weeks after treatment with both TACE plus Endostar and with TACE alone (P < 0.01). Although there was no statistically significant difference in tumor size between the group with TACE plus Endostar and the group with TACE alone (P > 0.05), MVD and VEGF were significantly less expressed in the TACE plus Endostar group than both groups with TACE alone and the control group (P < 0.01). Blood flow (BF), blood volume (BV), and permeability-surface area products (PS) in the group with TACE plus Endostar on perfusion CT were significantly higher than other two groups (P < 0.05), which were positively correlated with the MVD and VEGF values (P < 0.05). Conclusions TACE with arterial administration of Endostar simultaneously significantly inhibited the angiogenesis biomarkers associated with TACE in a rabbit model bearing VX2 liver tumor, which indicates that the combined treatment protocol may have potential synergistic effects on liver cancer. It also is suggested that perfusion CT may be useful for monitoring antiangiogenic/antivascular treatment in the liver tumors.
引用
收藏
页码:824 / 832
页数:9
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