Inhibition of angiogenesis and HCT-116 xenograft tumor growth in mice by kallistatin

被引:23
|
作者
Diao, Yong [1 ]
Ma, Jian
Xiao, Wei-Dong
Luo, Jia
Li, Xin-Yan
Chu, Kin-Wah
Fung, Peter Wc
Habib, Nagy
Farzaneh, Farzin
Xu, Rui-An
机构
[1] Huaqiao Univ, Inst Mol Med, Fujian 362021, Peoples R China
[2] Huaqiao Univ, Inst Mol Med, Engn Res Ctr, Minist Educ, Fujian 362021, Peoples R China
[3] Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
[4] Univ Penn, Dept Pediat, Philadelphia, PA 19104 USA
[5] Univ Chicago, Dept Pharm, Chicago, IL 60637 USA
[6] Univ London Imperial Coll Sci Technol & Med, Dept Transplantat, London, England
[7] Kings Coll London, Dept Haematol & Med, London SE5 9NU, England
基金
英国生物技术与生命科学研究理事会;
关键词
kallistatin; adeno-associated virus; angiogenesis inhibitors; colon; neoplasm;
D O I
10.3748/wjg.v13.i34.4615
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate the inhibitory effect of kallistatin (KAL) on angiogenesis and HCT-116 xenograft tumor growth. METHODS: Heterotopic tumors were induced by subcutaneous injection of 2 x 106 HCT-11 cells in mice. Seven days later, 2 x 10(11) rAAV-GFP or rAAV-KAL was injected intratumorally (n = 5 for each group). The mice were sacrificed at d 28, by which time the tumors in the rAAV-GFP group had grown to beyond 5% of the total body weight. Tumor growth was measured by calipers in two dimensions. Tumor angiogenesis was determined with tumor microvessel density (MVD) by immunohistology. Tumor cell proliferation was assessed by Ki-67 staining. RESULTS: Intratumor injection of rAAV-KAL inhibited tumor growth in the treatment group by 78% (171 52 mm(3)) at d 21 after virus infection compared to the control group (776 241 mm(3)). Microvessel density was significantly inhibited in tumor tissues treated with rAAV-KAL. rAAV-KAL also decreased the proportion of proliferating cells (Ki-67 positive cells) in tumors compared with the control group. CONCLUSION: rAAV-mediated expression of KAL inhibits the growth of colon cancer by reducing angiogenesis and proliferation of tumor cells, and may provide a promising anti-angiogenesis-based approach to the treatment of metastatic colorectal cancer. (c) 2007 WJG. All rights reserved.
引用
收藏
页码:4615 / 4619
页数:5
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