Colorectal Cancer
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 15, 2003; 9(2): 281-283
Published online Feb 15, 2003. doi: 10.3748/wjg.v9.i2.281
Effects of TNP-470 on proliferation and apoptosis in human colon cancer xenografts in nude mice
Zong-Hai Huang, Ying-Fang Fan, Hu Xia, Hao-Miao Feng, Fu-Xiang Tang
Zong-Hai Huang, Ying-Fang Fan, Hao-Miao Feng, Fu-Xiang Tang, Department of Surgery, Zhujiang Hospital, First Military Medical university, Guangzhou 510282, Guangdong Province, China
Hu Xia, Department of Respiratory Diseases, Zhujiang Hospital, First Military Medical University, Guangzhou 510282, Guangdong Province, China
Author contributions: All authors contributed equally to the work.
Supported by the Natural Science Foundation of Guangdong Province, No.013072
Correspondence to: Dr. Zong-Hai Huang, Department of Surgery, Zhujiang Hospital, First Military Medical University, Guangzhou 510282, Guangdong Province, China. hghigh@gdvnet.com
Telephone: +86-20-61643211
Received: July 31, 2002
Revised: August 4, 2002
Accepted: August 27, 2002
Published online: February 15, 2003
Abstract

AIM: To study the effect of TNP-470 on cell growth, proliferation and apoptosis in human colon cancer xenografts in nude mice.

METHODS: Human colon cancer xenografts were transplanted into 20 nude mice. Mice were randomly divided into two groups. TNP-470 treated group received TNP-470 (30 mg/kg, s.c) every other day and the control group received a sham injection of same volume saline solution. They were sacrificed after 4 wk and their tumors were processed for histological examination. The expression of proliferating cell nuclear antigen (PCNA) in tumors was detected using immunohistochemical method with image analysis, and apoptosis in tumor cells was measured by TdT-mediated biotinyated-dUTP nick end labeling (TUNEL) staining.

RESULTS: Comparing with controls, tumor growth was significantly inhibited in TNP-470 treated group, the inhibitory rate being 54.4%. Expression of PCNA in tumors of TNP-470 treated group (PI 54.32 ± 11.47) was significantly lower than that of control group (PI 88.54 ± 12.36), P < 0.01. Apoptosis index (AI) of TNP-470 treated group (18.95 ± 1.71) was significantly higher than that of control group (7.26 ± 1.44), P < 0.001, typical morphological change of apoptosis in tumor cells was observed in TNP-470 treated group.

CONCLUSION: Besides the anti-angiogenic effects, TNP-470 can inhibit tumor growth by inhibiting the proliferation and inducing apoptosis of tumor cells.

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