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World J Gastroenterol. Dec 14, 2007; 13(46): 6249-6253
Published online Dec 14, 2007. doi: 10.3748/wjg.v13.i46.6249
Effects of endogenous nitric oxide induced by 5-fluorouracil and L-Arg on liver carcinoma in nude mice
Xiao-Yan Yin, Jun-Mei Jiang, Ji-Yong Liu, Ju-Ren Zhu
Xiao-Yan Yin, Endoscopy Center, Affilated Hospital of Medical College, Qingdao University, Qingdao 266003, Shandong Province, China
Jun-Mei Jiang, Ji-Yong Liu, Ju-Ren Zhu, Department of Gastroenterology, Shandong Provincial Hospital, Jinan 250021, Shandong Province, China
Author contributions: All authors contributed equally to the work.
Supported by the Grants for the Excellent Youth Scientists of Shandong Provincial Science Commission. No. 2000BB2DBA1
Correspondence to: Dr. Jun-Mei Jiang, Department of Gastroenterology, Shandong Provincial Hospital, Jinan 250021, Shandong Province, China. jiangjunm@hotmail.com
Telephone: +86-532-82911525 Fax: +86-532-82911999
Received: April 11, 2007
Revised: September 1, 2007
Accepted: October 26, 2007
Published online: December 14, 2007
Abstract

AIM: To study the effects of endogeous nitric oxide induced by 5-fluorouracil (5-FU) and L-arginine (L-Arg) on the human liver carcinoma model in nude mice.

METHODS: The human liver carcinoma model in nude mice was established with BEL-7402 cells and normal saline (NS), 5-FU and 5-FU + L-Arg injected intraperitoneally. The tumor size was measured. The necrotic degree and range were observed under microscope. The apoptosis of cancer cell was detected by turmina deoxynucleotidyl transferanse mediated dUTP nick end labeling (TUNEL) method. Immunohistochemical method was performed to determine the expression of iNOS, P16, BAX. The chemical colorimetry was used to test the activity and nitrate reductase method was adopted to test the concentration of nitric oxide (NO) in the tumor tissue. The BI2000 pathological image analyzer was used to analyze the result of immunohistochemistry.

RESULTS: 5-FU combined with L-Arg could inhibit the tumor growth apparently. In NS, 5-FU and 5-FU+L-Arg groups, the changes of tumor volumes were 257.978 ± 59.0, 172.232 ± 66.0 and 91.523 ± 26.7 mm3, respectively (P < 0.05 5-FU vs 5-FU + L-Arg group; P < 0.05 NS vs 5-FU + L-Arg group; P < 0.05, NS vs 5-FU group). The necrotic range and apoptosis index were significantly increased after the drug injection. The necrotic range was biggest in 5-FU + L-Arg group (χ2 = 15.963, P < 0.05).

The apoptosis indexes were as follows: NS, 17.4% ± 6.19%; 5-FU, 31.3% ± 12.3%; and 5-FU + L-Arg, 46% ± 15.24% (P < 0.05, 5-FU vs 5-FU + L-Arg; P < 0.05, NS vs 5-FU + L-Arg; P < 0.05, NS vs 5-FU). The expression and activity of iNOS were increased in the tumor tissue. The concentration of NO was also increased. F of optical density of iNOS, iNOS activity and NO concentration are 31.693, 21.949, and 33.909, respectively, P < 0.05. The concentration of NO was related to the expression of P16 and BAX. The correlation coefficient was 0.764 and 0.554.

CONCLUSION: 5-FU combined with L-Arg can inhibit the growth of tumor in nude mice. The effect may be related to inducing the synthesis and increasing the activity of iNOS. The production of NO is increased, and it can enhance the expression of apoptosis-related gene and antioncogene.

Keywords: 5-Fluorouracil, L-Arginine, Animal model, Nitric oxide synthase, Nitric oxide