目的 研究pcDNA3/AFP/TK/Angio融合基因?qū)θ烁伟┘?xì)胞系SMMC-7721裸鼠移植瘤模型的靶向性治療作用。
方法 建立人原發(fā)性肝癌裸鼠皮下移植瘤模型,將荷瘤裸鼠隨機(jī)分成腫瘤對(duì)照組、空質(zhì)粒組、丙氧鳥(niǎo)苷(GCV)組、pcDNA3/TK/Angio組及pcDNA3/AFP/TK/Angio組5組。于瘤體內(nèi)分別直接注射不同的質(zhì)粒,同時(shí)于裸鼠腹腔內(nèi)注射GCV,觀察不同時(shí)段皮下腫瘤的生長(zhǎng)情況并做病理學(xué)檢查,免疫組化法檢測(cè)腫瘤微血管密度(MVD)以及血管內(nèi)皮細(xì)胞生長(zhǎng)因子(VEGF)的表達(dá)量,原位末端標(biāo)記(TUNEL)法檢測(cè)細(xì)胞原位凋亡。放免法檢測(cè)裸鼠血清甲胎蛋白(AFP)的變化,透射電鏡觀察腫瘤細(xì)胞超微結(jié)構(gòu)的變化。
結(jié)果 裸鼠皮下成瘤率100%; pcDNA3/TK/Angio組及pcDNA3/AFP/TK/Angio組的腫瘤體積、血清AFP含量、腫瘤MVD和VEGF表達(dá)強(qiáng)度均明顯低于對(duì)照組、空質(zhì)粒組和GCV組(P<0.05),細(xì)胞凋亡指數(shù)都明顯高于后3組(P<0.05),可見(jiàn)較多的凋亡細(xì)胞。而pcDNA3/AFP/TK/Angio組的腫瘤體積、AFP、MVD及VEGF表達(dá)強(qiáng)度又明顯低于pcDNA3/TK/Angio組(P<0.05),凋亡指數(shù)高于后者(P<0.05)。
結(jié)論 pcDNA3/AFP/TK/Angio融合基因系統(tǒng)可顯著抑制腫瘤的生長(zhǎng),有望成為治療原發(fā)性肝癌的新型生物制劑之一。
引用本文: 盛勤松,王琳,任鋒,盧永剛,鄒浩,肖曙峰,唐波,黃潔,張捷. pcDNA3/AFP/TK/Angio融合基因靶向性治療人原發(fā)性肝癌的實(shí)驗(yàn)研究. 中國(guó)普外基礎(chǔ)與臨床雜志, 2007, 14(4): 403-408. doi: 復(fù)制
版權(quán)信息: ?四川大學(xué)華西醫(yī)院華西期刊社《中國(guó)普外基礎(chǔ)與臨床雜志》版權(quán)所有,未經(jīng)授權(quán)不得轉(zhuǎn)載、改編
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- 1. Choi EA, Lei H, Maron DJ, et al. Combined 5-fluorouracil/systemic interferon-beta gene therapy results in long-term survival in mice with established colorectal liver metastases [J] . Clin Cancer Res, 2004; 10(4)∶1535.
- 2. Hwang KS, Cho WK, Yoo J, et al. Adenovirus-mediated interleukin-12 gene transfer combined with cytosine deaminase followed by 5-fluorocytosine treatment exerts potent antitumor activity in Renca tumor-bearing mice [J] . BMC Cancer, 2005; 5(1)∶51.
- 3. You TG, Wang HS, Yang JH, et al. Transfection of IL-2 and/or IL-12 genes into spleen in treatment of rat liver cancer [J] . World J Gastroenterol, 2004; 10(15)∶2190.
- 4. Chang CJ, Chen YH, Huang KW, et al. Combined GM-CSF and IL-12 gene therapy synergistically suppresses the growth of orthotopic liver tumors [J] . Hepatology, 2007; 45(3)∶746.
- 5. 黃畦, 陳大瑜, 付向?qū)? 等. 雙自殺基因重組腺病毒對(duì)肺癌細(xì)胞的殺傷作用 [J] . 中華實(shí)驗(yàn)外科雜志, 2006; 23(4)∶579.
- 6. 李梅生, 梁力建, 黃潔夫, 等. HSV-tk/CD融合基因殺傷人膽管癌細(xì)胞QBC939的體內(nèi)實(shí)驗(yàn) [J] . 中國(guó)普外基礎(chǔ)與臨床雜志, 2005; 12(6)∶581.
- 7. Li PY, Lin JS, Feng ZH, et al. Combined gene therapy of endostatin and interleukin 12 with polyvinylpyrrolidone induces a potent antitumor effect on hepatoma [J] . World J Gastroenterol, 2004; 10(15)∶2195.
- 8. Tai KF, Chen PJ, Chen DS, et al. Concurrent delivery of GM-CSF and endostatin genes by a single adenoviral vector provides a synergistic effect on the treatment of orthotopic liver tumors [J] . J Gene Med, 2003; 5(5)∶386.
- 9. Shi M, Wang FS, Wu ZZ. Synergetic anticancer effect of combined quercetin and recombinant adenoviral vector expressing human wild-type p53, GM-CSF and B7-1 genes on hepatocellular carcinoma cells in vitro [J] . World J Gastroenterol, 2003; 9(1)∶73.
- 10. Sung MW, Yeh HC, Thung SN, et al. Intratumoral adenovirus-mediated suicide gene transfer for hepatic metastases from colorectal adenocarcinoma: results of a phase Ⅰ clinical trial [J] . Mol Ther, 2001; 4(3)∶182.
- 11. Xu R, Sun X, Tse LY, et al. Long-term expression of angiostatin suppresses metastatic liver cancer in mice [J] . Hepatology, 2003; 37(6)∶1451.
- 12. 李曉, 王琳, 郭永章, 等. 血管生成抑制素基因?qū)β闶笕烁伟┮浦擦龅闹委熥饔?[J] . 中華實(shí)驗(yàn)外科雜志, 2004; 21(7)∶875 .
- 13. Shi YJ, Gong JP, Liu CA, et al. Construction of a targeting adenoviral vector carrying AFP promoter for expressing EGFP gene in AFP-producing hepatocarcinoma cell [J] . World J Gastroenterol, 2004; 10(2)∶186.
- 14. Huang X, Zhang W, Wakimoto H, et al. Adenovirus-mediated tissue-specific cytosine deaminase gene therapy for human hepatocellular carcinoma with different AFP expression levels [J] . J Exp Ther Oncol, 2002; 2(2)∶100.
- 15. Ohguchi S, Nakatsukasa H, Higashi T, et al. Expression of alpha-fetoprotein and albumin genes in human hepatocellular carcinomas: limitations in the application of the genes for targeting human hepatocellular carcinoma in gene therapy [J] . Hepatology, 1998; 27(2)∶599.