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5-氟尿嘧啶和L-精氨酸诱导内源性一氧化氮对裸鼠肝癌的影响。

Effects of endogenous nitric oxide induced by 5-fluorouracil and L-Arg on liver carcinoma in nude mice.

作者信息

Yin Xiao-Yan, Jiang Jun-Mei, Liu Ji-Yong, Zhu Ju-Ren

机构信息

Endoscopy Center, Affilated Hospital of Medical College, Qingdao University, Qingdao 266003, Shandong Province, China.

出版信息

World J Gastroenterol. 2007 Dec 14;13(46):6249-53. doi: 10.3748/wjg.v13.i46.6249.

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 mm(3), 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 (c2 = 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.

摘要

目的

研究5-氟尿嘧啶(5-FU)和L-精氨酸(L-Arg)诱导内源性一氧化氮对裸鼠人肝癌模型的影响。

方法

用BEL-7402细胞和生理盐水(NS)建立裸鼠人肝癌模型,分别腹腔注射5-FU、5-FU+L-Arg。测量肿瘤大小。在显微镜下观察坏死程度和范围。采用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)法检测癌细胞凋亡。采用免疫组化法检测诱导型一氧化氮合酶(iNOS)、P16、BAX的表达。用化学比色法检测活性,采用硝酸还原酶法检测肿瘤组织中一氧化氮(NO)浓度。用BI2000病理图像分析仪分析免疫组化结果。

结果

5-FU联合L-Arg能明显抑制肿瘤生长。在NS、5-FU和5-FU+L-Arg组中,肿瘤体积变化分别为257.978±59.0、172.232±66.0和91.523±26.7mm³(P<0.05,5-FU组与5-FU+L-Arg组比较;P<0.05,NS组与5-FU+L-Arg组比较;P<0.05,NS组与5-FU组比较)。注射药物后坏死范围和凋亡指数显著增加。5-FU+L-Arg组坏死范围最大(χ²=15.963,P<0.05)。凋亡指数如下:NS组为17.4%±6.19%;5-FU组为31.3%±12.3%;5-FU+L-Arg组为46%±15.24%(P<0.05,5-FU组与5-FU+L-Arg组比较;P<0.05,NS组与5-FU+L-Arg组比较;P<0.05,NS组与5-FU组比较)。肿瘤组织中iNOS的表达和活性增加。NO浓度也增加。iNOS光密度、iNOS活性和NO浓度的F值分别为31.693、21.949和33.909,P<0.05。NO浓度与P16和BAX的表达相关。相关系数分别为0.764和0.554。

结论

5-FU联合L-Arg可抑制裸鼠肿瘤生长。其作用可能与诱导iNOS合成和增加其活性有关。NO生成增加,可增强凋亡相关基因和抗癌基因的表达。

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