期刊文献+

DCE-MRI定量参数K^(trans)值评估抗血管生成药物治疗裸鼠胃癌原位移植瘤的疗效 被引量:10

K^(trans) of dynamic contrast enhanced MRI in evaluation of anti-angiogenic effects on nude mice with orthotopic transplantation tumor model of gastric cancer
下载PDF
导出
摘要 目的分析MR动态增强扫描(DCE-MRI)定量参数Ktrans值评估甲磺酸阿帕替尼治疗裸鼠胃癌原位移植瘤的疗效。方法建立裸鼠胃癌原位移植瘤模型后,随机分为治疗组(n=15,胃内灌注甲磺酸阿帕替尼100mg/kg体质量)和对照组(n=15,胃内灌注无菌去离子水),治疗18天后行DCE-MRI,并定量测量Ktrans值。检查结束后,取出瘤体测量微血管密度(MVD)值和血管内皮生长因子(VEGF)水平,并对比组间差异。结果与对照组相比,治疗组MVD值(χ2=4.89,P<0.05)、VEGF水平明显减低(χ2=8.69,P<0.01),治疗组Ktrans值[(0.63±0.05)/min]明显低于对照组[(1.66±0.23)/min;t=17.05,P<0.01]。结论 DCE-MRI定量参数Ktrans值可作为胃癌抗血管生成药物甲磺酸阿帕替尼疗效的评估指标。 Objective To assess the feasibility of K value of dynamic contrast enhanced MRI (DCE-MRI) in evaluation of anti-angiogenic effects on nude mice with orthotopic transplantation tumor model of gastric cancer. Methods Nude mice with orthotopic transplantation tumor model of gastric cancer were randomly assigned to two groups: Treatment group (n = 15), mice were given apatinib intragastrically for 18 days (100 mg/kg), and control group (n= 15), mice were given ddH202 in the same manner. After 18 days, DCE-MRI was performed and K value was measured. Then the tumors were dissected from the adjacent tissues in order to detect the microvessel density (MVD) and vascular endothelial growth factor (VEGF) expression levels. MVD and VEGF expression level were compared between treatment group and the con- trol group. Results MVD (x22 =4.89, P(0.05) and VEGF expression level (x2=8.69, P(0.01) of treatment group were much lower than those of control groups. The Kt value of treatment group was significantly lower than that of con- trol groups ([0.63±0.05]/min vs [1.66±0.23]/min, t=17.05, P〈0.01). Conclusion The value of k in DCE-MRI can be utilized to assess the effects of apatinib on nude mice with orthotopic transplantation model of gastric cancer.
出处 《中国医学影像技术》 CSCD 北大核心 2017年第6期843-847,共5页 Chinese Journal of Medical Imaging Technology
关键词 磁共振成像 胃肿瘤 模型 动物 血管生成抑制剂 Magnetic resonance imaging Stomach neoplasms Models, animal Angiogenesis inhibitors
  • 相关文献

参考文献3

二级参考文献44

  • 1[1]Minsky BD,Cohen AM.Blood vessel invasion in colorectal cancer-an alternative to TNM staging? Ann Surg Oncol 1999; 6:129-130
  • 2[2]Mullis KB.Target amplification for DNA analysis by the polymerase chain reaction.Ann Biol Clin (Paris) 1990; 48:579-582
  • 3[3]Majima T,Ichikura T,Takayama E,Chochi K,Mochizuki H.Detecting circulating cancer cells using reverse transcriptasepolymerase chain reaction for cytokeratin mRNA in peripheral blood from patients with gastric cancer.Jpn J Clin Oncol 2000;30:499-503
  • 4[4]Wildi S,Kleeff J,Maruyama H,Maurer CA,Friess H,Buchler MW,Lander AD,Korc M.Characterization of cytokeratin 20 expression in pancreatic and colorectal cancer.Clin Cancer Res 1999; 5:2840-2847
  • 5[5]McDonnell CO,Hill AD,McNamara DA,Walsh TN,Bouchier-Hayes DJ.Tumour micrometastases:the influence of angiogenesis.Eur J Surg Oncol 2000; 26:105-115
  • 6[6]Duff SE,Li C,Garland JM,Kumar S.CD105 is important for angiogenesis:evidence and potential applications.FASEB J 2003; 17:984-992
  • 7[7]Vlems FA,Diepstra JH,Cornelissen IM,Ruers TJ,Ligtenberg MJ,Punt CJ,van Krieken JH,Wobbes T,van Muijen GN.Limitations of cytokeratin 20 RT-PCR to detect disseminated tumour cells in blood and bone marrow of patients with colorectal cancer:expression in controls and downregulation in tumour tissue.Mol Pathol 2002; 55:156-163
  • 8[8]Hyung WJ,Lee JH,Choi SH,Min JS,Noh SH.Prognostic impact of lymphatic and/or blood vessel invasion in patients with node-negative advanced gastric cancer.Ann Surg Oncol 2002; 9:562-567
  • 9[9]Birner P,Obermair A,Schindl M,Kowalski H,Breitenecker G,Oberhuber G.Selective immunohistochemical staining of blood and lymphatic vessels reveals independent prognostic influence of blood and lymphatic vessel invasion in earlystage cervical cancer.Clin Cancer Res 2001; 7:93-97
  • 10[10]Soeth E,Roder C,Juhl H,Kruger U,Kremer B,Kalthoff H.The detection of disseminated tumor cells in bone marrow from colorectal-cancer patients by a cytokeratin-20-specific nested reverse-transcriptase-polymerase-chain reaction is related to the stage of disease.Int J Cancer 1996; 69:278-282

共引文献35

同被引文献73

引证文献10

二级引证文献62

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