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. 2002 Oct;8(5):853-6.
doi: 10.3748/wjg.v8.i5.853.

Angiogenesis inhibitor TNP-470 suppresses growth of peritoneal disseminating foci of human colon cancer line Lovo

Affiliations

Angiogenesis inhibitor TNP-470 suppresses growth of peritoneal disseminating foci of human colon cancer line Lovo

Ying-Fang Fan et al. World J Gastroenterol. 2002 Oct.

Abstract

Aim: To study the effect of angiogenesis inhibitor TNP-470 on peritoneal dissemination of colon cancer in nude mice.

Methods: The MTT assay was used to evaluate the inhibitory effect of TNP-470 on human colon cancer cell line Lovo. Lovo cells were injected into the peritoneal cavity of BABL/C nu/nu mice and the models of peritoneal dissemination were developed. Thirty nude mice were randomly divided into control and TNP-470-treated group. In TNP-470-treated group, TNP-470 was injected subcutaneously every other day from day 1 until sacrifice or death (30 mg x kg(-1)). The control group received a sham injection of the same volume saline solution.

Results: In vitro, TNP-470 inhibited the growth of Lovo cells, with its IC50 at 2.14 X 10(2) microg x L(-1). In vitro, TNP-470 demonstrated growth inhibition of tumors. Mice body weight and abdominal circumferences were significantly different between TNP-470-treated group (24.5+/-3.2 g, 7.0+/-1.1 cm) and control group (29.5+/-2.1 g, 10.3+/-1.5 cm), P=0.005 and P=0.001. The number of disseminated foci was significantly different between the control group (92.1+/-20.6) and the TNP-470-treated group (40.3+/-12.3), P<0.001. The maximal size of foci was significantly smaller in TNP-470-treated group (3.3+/-0.7 mm) than that of control (7.3+/-2.3 mm), P=0.004. Mean survival time was significantly longer in TNP-470-treated group(98.00+/-12.06 d) than that in control group (41.86+/-9.51 d), P<0.001.

Conclusion: Angiogenesis inhibitor TNP-470 might be effective in treating peritoneal dissemination of colon cancer and improve the survival rate of nude mice.

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Figures

Figure 1
Figure 1
Inhibition curve of Lovo cells after TNP-470 treated 48 h.
Figure 2
Figure 2
Survival curves in the control and TNP-470-treated groups

References

    1. Fan YF, Huang ZH. Progress in the studies of gene therapy for colorectal cancer. Shijie Huaren Xiaohua Zazhi. 2001;9:427–430.
    1. Liu H, Wu JS, Li LH, Yao X. The expression of Platelet-derived growth factor and angiogenesis in human colorectal carcinoma. Shijie Huaren Xiaohua Zazhi. 2000;8:661–664.
    1. Wu J, Fan DM. Neoplastic vascularization and vascular inhibitory treatment. Shijie Huaren Xiaohua Zazhi. 2001;9:316–321.
    1. Blood CH, Zetter BR. Tumor interactions with the vasculature: angiogenesis and tumor metastasis. Biochim Biophys Acta. 1990;1032:89–118. - PubMed
    1. Kusaka M, Sudo K, Matsutani E, Kozai Y, Marui S, Fujita T, Ingber D, Folkman J. Cytostatic inhibition of endothelial cell growth by the angiogenesis inhibitor TNP-470 (AGM-1470) Br J Cancer. 1994;69:212–216. - PMC - PubMed

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