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兔胰头癌动物模型的建立 被引量:2

Establishment of pancreatic head cancer model in rabbits
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摘要 目的:建立稳定可靠的兔胰头癌动物模型,选择最佳的模型制作方法。方法:48只兔采用随机区组方法分为两组,每组24只,分别采用瘤块悬液法、瘤块植入法将肿瘤细胞注射至胰头内制作兔胰腺癌动物模型,计量数据比较采用双因素完全随机设计方差分析,分别于1、2、3和4周处死大白兔行移植组织解剖和病理学检查,观察2种不同建模方式的肿瘤生长情况及生物学形态。结果:建模过程中,2种方法成瘤率均为100%。瘤块植入法术后1周肿瘤体积为(0.90±0.13)cm3,离散系数为0.14;第2周肿瘤体积为(3.44±0.41)cm3,离散系数为0.12;第3周肿瘤体积为(7.53±0.69)cm3,离散系数为0.09;第4周肿瘤体积为(36.75±5.93)cm3,离散系数为0.16。瘤块悬液法术后1周肿瘤体积为(1.15±0.21)cm3,离散系数为0.18;第2周肿瘤体积为(4.94±1.64)cm3,离散系数为0.33;第3周肿瘤体积为(9.47±4.26)cm3,离散系数为0.45;第4周肿瘤体积为(46.31±16.77)cm3,离散系数为0.36。对术后肿瘤体积进行比较:1)瘤块植入法离散系数较小,生长相对稳定;2)生长时间对肿瘤生长体积具有显著影响,F=78.569 4,P=0.002 4;而生长时间与建模方法的交互作用对肿瘤生长体积无显著影响,P>0.05。术后第1周两组动物均未发现转移,瘤块植入法第2周未见种植性转移,第3周5只大白兔(83.33%)大网膜出现转移,瘤块悬液法第2周1只大白兔(16.67%)出现结肠、肓肠及腹壁种植转移,第3周4只大白兔(66.67%)出现结肠、盲肠及腹壁种植转移,2只大白兔(33.33%)出现大网膜转移。微观病理显示,瘤块与种植前瘤块病理形态基本一致,大部分瘤块悬液法HE染色下图像可见中间有较多坏死组织。瘤块植入法较瘤块悬液法肿瘤生长更为稳定。结论:成功建立了兔胰头癌动物模型,瘤块植入法是建立兔胰头癌动物模型的较佳方法。 OBJECTIVE:To establish a stable and reliable model of pancreatic head cancer in rabbits,and find out a optimal method of establishing model. MTHODS: Forty-eight rabbits were divided into 2 groups randomly with 24 in each. With injection of tumor tissue mass suspension and implantation of tumor tissue, tumor cells were injected respectively in- to the rabbits of the 2 groups. Analysis of two-factor randomized design variance was used for data measurement. The rab- bits were sacrificed at the l st,the 2nd, the 3rd and the 4th week for anatomy and pathological examination of the trans- planted tumors. Two established models were employed to observe the tumor growth and the biological features. RE- SULTS: Models were established successfully by injection of tumor tissue mass suspension and implantation of tumor tis- sue. Postoperative tumor volume of the two groups was detected respectively. Tumor volume in implantation of tumor tissue group were (0.90±0. 13) cm3 ,(3.44±0.41) cm3 ,(7.53±0.69) cm3 ,(36.75±5.93) cm3 at the lst,the 2nd,the 3rd and the 4th week after operation respectively, and dispersion coefficient were 0. 14,0.12,0.09,0.16;and tumor volume in tumor tissue mass suspension group were (1. 15 ± 0. 21) cm3 , (4. 94 ± 1. 64) cm3 , (9. 47 ± 4.26) cm3, (46.31±16.77) cm3 ,and dispersion coefficient were 0. 18,0.33,0.45,0. 36. The postoperative tumor volume of the two groups was compared, and the results examined by Two-factor analysis of variance were as follows:Dispersion coefficient in the implantation of tumor tissue group was small which indicates that the tumor growth was relatively stable. The growth time of F value was 78. 569 4,the P value was 0. 002 4,which indicated that the growth time had significant effect on the growth of tumor volume. The interaction growth time and methods of establishing model on the growth of tumor volume did not have a significant impact,because the P values were 0. 215 1 and 0. 298 1. There was no metastasis found in both groups at 1st week after operation. There was no metastasis found at 2nd week, and omentum metastasis was found in 5 rabbits (83.33%) at the 3rd week in implantation of the tumor tissue group. In injection of tumor tissue mass suspension group,1 rabbit (16.67%) in the 2nd week and 4 rabbits (66.67%) in the 3rd week were found metastasis in colon, cecum,and abdominal wall,and 2 rabbits (33.33%) were found metastasis in omentum at the 3rd week. Miroscopic pa- thology in tumor block showed the same results as primary tumor, and more necrotic tissues were found in most of the ani mals in injection of tumor tissue mass suspension group by the HE staining. Tumor tissues proliferated more stably by u sing the implantation of tumor tissue method. CONCLUSION: The model of cancer of pancreatic head in rabbits is estab- lished successfully in this study and the results showed that the implantation of tumor tissue is a better method.
出处 《中华肿瘤防治杂志》 CAS 北大核心 2013年第23期1797-1802,共6页 Chinese Journal of Cancer Prevention and Treatment
关键词 胰腺肿瘤 病理学 VX2肿瘤模型 瘤块植入法 瘤块悬液法 pancreatic neoplasms/pathology tumor model of VX2 tumor tissue mass suspension tumor tissue rabbits
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参考文献20

  • 1Gillen S, Schuster T, Friess H, et al. Palliative resections versus palliative bypass procedures in pancreatic cancer-a systematic re- view[J]. Am J Surg, 2012,203(4) : 496-502.
  • 2Heinemann V, Vehling-Kaiser U, Waldschmidt D, et al. Gemeit- ahine plus erlotinib followed by capecitabine versus capecitabine plus erlotinib followed by gemcitabine in advanced pancreatic cancer : final results of a randomised phasetrial of the ' Arbeitsge- meinschaft Internistische Onkologie' (AIO-PK0104) [J]. Gut, 2013,62(5) :751-759.
  • 3Poruk KE, Firpo MA, Adler DG, et al. Screening for pancreatic cancer:why,how,and who[J]. Ann Surg,2013,257(1) :17-26.
  • 4Michl P, Gress TM. Current concepts and novel targets in a& vanced pancreatic cancer[J]. Gut,2013,62(2) :317-326.
  • 5Hartman DJ,Krasinskas AM. Assessing treatment effect in pan- creatic cancer[J]. Arch Pathol Lab Meal,2012,136(1) :100-109.
  • 6Jemal A, Sieqel R, Xu J, et al. Cancer statistics, 2010[J]. CA Cancer J Clin,2010,60(5) :277-300.
  • 7Lieher M, Mazzetta J, Nelson-Rees W, et al. Establishment of a continuous tumor-cell line (panc-1)from a human carcinoma of the exocrine pancreas[J]. Int J Cancer, 1975,15(5) : 741-747.
  • 8Akagi T, Kimoto T. Establishment and characteristics of a hu- man pancreatic cancer cell line(HCG-25) [J]. Acta Pathol Jan, 1977,27(1) :51-58.
  • 9Antonic C,Busnardo M D, Liberato J A, et al. History of the pan-creas[J]. Am J Surg, 1983,146(5) :539-550.
  • 10李杰,童春帆,李强.胰腺癌组织MMP-2表达及其意义的探讨[J].中华肿瘤防治杂志,2010,17(21):1761-1763. 被引量:5

二级参考文献11

  • 1肖春花,冯玉梅,李晓青,郝希山.基质金属蛋白酶2 mRNA表达量与乳腺癌转移的关系及临床意义[J].中华外科杂志,2005,43(9):599-602. 被引量:4
  • 2杨锦建,张秋红,贾占奎,周四维.基质金属蛋白酶(MMP)9、MMP2 mRNA及基质金属蛋白酶抑制剂2 mRNA在人膀胱移行细胞癌中的表达及意义[J].中华实验外科杂志,2006,23(4):594-595. 被引量:33
  • 3Dunne AA, Schmidt A, Kuropkat C, et al. The auricular VX2 carcinoma--an animal model for sentinel node concept. In Vivo, 2003, 17: 457-461.
  • 4Easty DM, Easty GC. Establishment of an in vitro cell line from the rabbit VX2 carcinoma. Virchows Arch B Cell Pathol Incl Mol Pathol,1982,39: 333-337.
  • 5Dunne AA, Mandic R, Ramaswamy A, et al. Lymphogenic metastatic spread of auricular VX2 carcinoma in New Zealand white rabbits.Anticancer Res, 2002, 22(6A): 3273-3279.
  • 6van Es RJ, Franssen O, Dullens HF, et al. The VX2 carcinoma in the rabbit auricle as an experimental model for intra-arterial embolization of head and neck squamous cell carcinoma with dextran microspheres.Lab Anim, 1999 , 33: 175-184.
  • 7van Es RJ, Dullens HF, van der Bilt A, et al. Evaluation of the VX2 rabbit auricle carcinoma as a model for head and neck cancer in humans. J Maxillofac Surg, 2000, 8: 300-307.
  • 8Dunne AA, Plehn S, Schulz S, et al. Lymph node topography of the head and neck in New Zealand White rabbits. Lab Anim,2003,37: 37-43.
  • 9Mandic R, Dunne AA, Eikelkamp N, et al. Expression of MMP-3, MMP-13, TIMP-2 and TIMP-3 in the VX2 carcinoma of the New Zealand white rabbit.Anticancer Res, 2002, 22(6A): 3281-3284.
  • 10郑献召,李珊珊,轩小燕,李娜,王丰.食管鳞癌组织中S100A4和MMP2蛋白表达与临床病理学特征的关系[J].世界华人消化杂志,2007,15(31):3338-3342. 被引量:3

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