期刊文献+

隐形顺铂聚乳酸纳米微粒联合nm23-H_1基因对口腔癌靶向治疗的实验研究 被引量:1

The experimental study of cisplatin loaded polylactic acid-polyethylene glycol nanoparticles and nm23-H_1 gene combined targeted therapy for oral carcinoma
原文传递
导出
摘要 目的:评价隐形顺铂聚乳酸纳米微粒(CDDP-PLA-PEG-NP)联合nm23-H1基因对口腔癌靶向治疗的疗效。方法:用DMBA诱导建立金黄地鼠口腔颊癌模型,30只颊癌金黄地鼠随机分为3组,每组10只:①实验组:PEG-CDDP-PLA-NP静脉注射+脂质体包裹的Adeasy-nm23-H1质粒瘤内注射;②对照组Ⅰ:单行脂质体包裹的Adeasy-nm23-H1质粒瘤内注射;③对照组Ⅱ:单行PEG-CDDP-PLA-NP静脉注射。比较3组癌细胞的凋亡情况。结果:实验组、对照组Ⅰ和对照组Ⅱ完成治疗后癌细胞凋亡指数(AI)分别为31.46±2.371、0.04±1.422、2.63±1.96。实验组癌细胞凋亡指数显著高于对照组Ⅰ和对照组Ⅱ(P<0.05)。结论:隐形顺铂聚乳酸纳米微粒联合nm23-H1基因较单一nm23-H1基因治疗或隐形纳米靶向治疗显著地提高了对口腔癌的治疗效果,该方法有较大的发展前景。 Objective: To investigate therapeutic effect of Cisplatin loaded polylactic acid- polyethylene glycol nanoparticles(CDDP-PLA-PEG-NP) and nm23-H1 gene combinedtargeted therapy for oral carcinoma.Method:In DMBA-induces hamstersm oral carcinoma, 30 model hamsters were divided randomly into three groups far 10 animals in each group: ①ⅠGroup was treated with CDDP-PLA-PEG-NP plus nm23-H1 gene; ②ⅡGroup was treated with nm23-H1 gene alone;③ Ⅲ Group was treated with CDDP-PLA-PEG-NP alone. Apoptosis in tumor cells was compared among three groups.Result:Apoptoti index of Ⅰ-Ⅲ groups were 31.46±2.37,10.04±1.42 and 22. 63 ± 1.96 respectively; Apoptotic index of Ⅰ group was significantly higher than that of Ⅱ group and Ⅲ Group( P 〈 0.05). Conclusion: In comparison with nm23-H1 gene treatmeat alone or CDDP-PLA-PEG-NP treatmeat alone, CDDP-PLA-PEG-NP plus nm23-H1 gere can significantly increase therapeutic effect far oral carcinoma, this kind of treatmeat model is worth further exploring.
出处 《临床口腔医学杂志》 2006年第7期392-394,共3页 Journal of Clinical Stomatology
基金 重庆市科委应用基础研究项目(2003-43) 重庆市卫生局科研项目(2001年) 重庆医科大学科技基金(XB200207)
关键词 隐形纳米/长循环纳米 NM23-H1基因 顺铂 肿瘤 口腔 stealth nanoparticles/Long-circulating nanoparticles nm23-H1 gene cisplatin neoplasm oral cavity
  • 相关文献

参考文献9

二级参考文献28

  • 1景纯,温玉明,王大章,王昌美.人体口腔颊、舌部淋巴管的结构特点及分布与癌转移[J].华西口腔医学杂志,1995,13(2):125-129. 被引量:18
  • 2李龙江,温玉明,王昌美.颊癌微血管分支类型的动物实验研究[J].华西口腔医学杂志,1996,14(2):79-82. 被引量:3
  • 3[1]Develde CV. Lymphatic invasion and metastasis. Experientia, 1977,33(7):837- 844 被引量:1
  • 4[2]Weber E, Sacchi G, Comparini L. Plasticity of intercellular junctions of rat liver lympha capillaries in relation to functional conditions. Angiology, 1991, 42(11):929-934 被引量:1
  • 5[9]Tarrats A, Cot X, Lailla JM, et al. Endolymphatic chemotherapy in Gynecologic . Cancer, 1990,65(10):2213-2216 被引量:1
  • 6Parhar RS, Shi Y, Zou M, et al. Effects of cytokine-mediated modulation of nm23 expression on the invasion and metastatic behavior of B16F10 melanoma cells. Int J Cancer, 1995,60(2):204-210. 被引量:1
  • 7Freije JM, Lawrence JA, Hollingshead MG, et al. Identification of compounds with preferential inhibitory activity against low-Nm23-expressing human breast carcinoma and melanoma cell lines. Nat Med,1997,3(4) :395-401. 被引量:1
  • 8Caligo MA, Cipollini G, Fiore L, et al. NM23 gene expression correlates with cell growth rate and S-phase. Int J Cancer, 1995,60(6) : 837-842. 被引量:1
  • 9Iizuka N, Hirose K, Noma T, et al. The nm23-H1 gene as a predictor of sensitivity to chemotherapeutic agents in oesophageal squamous cell carcinoma. Br J Cancer, 1999,81 (3) :469-475. 被引量:1
  • 10Parhar RS, Shi Y, Zou M, et al. Effects of cytokine-- mediated modulation of nm23 expression on the invasion and metastatic behavior of B16F10 melanoma cells. Int J Cancer, 1995 ; 60(2):204. 被引量:1

共引文献41

同被引文献10

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部