期刊文献+

两种建立金黄地鼠颊囊癌模型方法的对照研究 被引量:2

Comparison between Two Methods of Establishing Induced Buckle Pouch Carcinogenesis Model in Syrian Golden Hamster
下载PDF
导出
摘要 目的二甲基苯并蒽丙酮注射法建立金黄地鼠颊囊癌动物模型,并与传统涂抹法相比较,为颊囊癌研究提供理想的动物模型。方法随机将81只金黄地鼠分为注射组、涂抹组和空白对照组。DM-BA丙酮注射组60只地鼠,将注射浓度预设为0.5%、0.4%、0.3%、0.2%、0.1%5个组,每组12只地鼠,每周两次,于注射后每周进行大体观察、监测体重并计算肿瘤生长率,至3、6、9、12周麻醉后各处死3只,进行组织学观察;涂抹组15只地鼠,以0.5%DMBA丙酮涂抹,每周三次,至6、9、12、15、18周后麻醉处死3只;空白对照组不做任何处理,于12周全部处死行组织学观察。结果注射浓度组0.4%、0.3%、0.2%、0.1%分别在13,9,12,16周时出现约为0.8 cm×0.6 cm×0.5 cm大小的肿瘤;12周时成瘤率分别为25%、87%、42%、58%;死亡率分别为48%、11%、13%、10%;相比0.5%DMBA丙酮涂抹组,12周时成瘤率为48%,死亡率为37%,至18周时才出现颊黏膜高分化鳞癌。结论经筛选采用0.3%DMBA丙酮液注射法可诱发形成口腔鳞癌动物模型,缩短建模周期,降低建模成本,能为科学研究提供较为理想的动物模型。 Objective To establish hamster buckle pouch carcinogenesis model with injection of DMBA acetone solution at different concentrations,and compares it with the traditional paint method.Methods Eighty one golden hamsters were assigned randomly into three groups: 60 hamsters in the injection groups were injected with DMBA acetone solution according at the concentrations of 0.5%,0.4%,0.3%,0.2%,0.1% respectively,twice a week,for 9 weeks.15 hamsters as the paint group were painted with 0.5% DMBA acetone solution,and 6 hamsters without any treatment belonged to the control group.General observation,weight,histopathology were executed every week.Three animals in every group were sacrificed by anesthesia at 3,6,9,12,18 weeks respectively and subjected to histological examination.Results The injection group with the concentration of 0.4%,0.3%,0.2%,0.1% appeared about 0.8 cm × 0.6 cm × 0.5 cm size of the tumor in 13,9,12,16 weeks respectively.The rate of carcinoma formation were 25%、87%、42% and 58% at 12 weeks.The mortality rate were 48%,11%,13% and 10% respectively.In the paint group tumor occurred in 18 weeks.The rate of carcinoma formation and mortality were 48% and 37% at 12 weeks.Conclusion The DMBA acetone solution at the concentration of 0.3% is more suitable for the formation of oral squamous cell carcinoma in golden hamster in the short term.This method is benefitial to shorten the feeding cycle,reducing the costs of the model.And it may provide an ideal animal model in vivo for further study.
出处 《肿瘤防治研究》 CAS CSCD 北大核心 2012年第3期267-271,共5页 Cancer Research on Prevention and Treatment
基金 国家重点基础研究发展计划资助项目(2010CB834202) 国家自然科学基金面上项目(30770639) 甘肃省自然科学基金项目资助(2010096RJ2A083) 兰州大学国家大学生创新性实验计划项目(20081073023)
关键词 金黄地鼠 鳞状细胞癌 动物模型 建立 Golden hamster Oral squamous cell carcinoma Animal model Establishment
  • 相关文献

参考文献13

  • 1Jamal A,Siegel R,Ward E,et al.Cancer statistics,2007[J].CACancer J Clin,2007,57(1):43-66.
  • 2Mork J,Lie AK,Glattre E,et al.Human papillomavirus infec-tion as a risk factor for squalors cell carcinoma of the head andneck[J].N Engl J Med,2001,344(15):1125-1131.
  • 3Mognetti B,Di Carlo F,Berta GN.Animal models in oral canc-er research[J].Oral Oncol,2006,42(5):448-460.
  • 4Vairaktaris E,Spyridonidou S,Papakosta V,et al.The hamstermodel of sequential oral oncogenesis[J].Oral Oncol,2008,44(4):315-324.
  • 5Lajolo C,Giuliani M,Sgambato A,et al.N-(4-hydroxyphenyl)all-trans-retinamide(4-HPR)high dose effect on DMBA in-duced hamster oral cancer:a histomorphometric evaluation[J].IntJ Oral Maxillofac Surg,2008,37(12):1133-1140.
  • 6Kim S.Animal models of cancer in the head and neck region[J].Clin Exp Otorhinolaryngol,2009,2(2):55-60.
  • 7Kanojia D,Vaidya MM.4-nitroquinoline-1-oxide induced ex-perimental oral carcinogenesis[J].Oral Oncol,2006,42(7):655-667.
  • 8Salley JJ.Experimental carcinogenesis in the cheek pouch ofthe Syrian hamster[J].J Dent Res,1954,33(2):253-262.
  • 9Bánóczy J,Csiba A.Occurrence of epithelial dysplasia in oral leuko-plakia.Analysis and follow-up study of 12 cases[J].Oral SurgOral Med Oral Pathol,1976,42(6):766-774.
  • 10周曾同,张水龙,王英,周永梅.金地鼠颊囊上皮异常增生12项病理特征的光镜分析[J].上海口腔医学,1997,6(1):32-35. 被引量:13

二级参考文献2

共引文献12

同被引文献26

  • 1董玉英,王洁,董福生,王旭,顾洪涛,候亚丽.颊癌P16及P53蛋白表达与临床病理的相关研究[J].现代口腔医学杂志,2006,20(5):519-522. 被引量:4
  • 2王照南,薄家璐,郭守明.短尾黑线仓鼠在医学上的应用[J].生物学通报,1997,32(3):14-15. 被引量:2
  • 3钟来平,郑家伟,张陈平,张志愿.口腔癌早期诊断的研究现状[J].中国口腔颌面外科杂志,2007,5(4):243-247. 被引量:14
  • 4Rahamthulla SA, Priya PV, of the supraomohyoid neck Hussain SM, et al. Effectiveness dissection in clinically NO neck patients with squamous cell carcinoma of buccal mucosa and gingivobuccal sulcus[J]. J Int Soc Prev Community Dent, 2015, 5(2): 131-140.
  • 5Xu Q, Gao Z, Tang D. Expression of E-cadherin and vimentin in oral squamous cell carcinoma[J]. Int J Clin Exp Pathol, 2015, 8(3): 3150-3154.
  • 6Ragin CC, Modugno F, Gollin SM. The epidemiology and risk factors of head and neck cancer: a focus on human papilloma virus[J]. J Dent Res, 2007, 86(2): 104-114.
  • 7Choi S, Myers JN. Molecular pathogenesis of oral squamous cell carcinoma: implications for therapy[J]. J Dent Res, 2008, 87(1): 14-32.
  • 8Gao Y, Zhang R, Zhang J, et al. Study of the extraction process and in vivo inhibitory effect of ganoderma triterpenes in oralmucosa cancer[J]. Molecules, 2011, 16(7): 5315-5332.
  • 9WHO Collaborating Centre for Oral Precancerous Lesions. Definition of leukoplakia and related lesions; an aid to studies on oralprecancer[J]. Oral Surg, 1978, 46(4): 518-539.
  • 10Kademani D, Bell RB, Scbmidt BL, et al. Oral and maxillofacial surgeons treating oral cancer: a preliminary report from the American association of oral and maxillofacial surgeons task force on oral cancer[J]. J Oral Maxillofac Surg, 2008, 66(10): 2151-2157.

引证文献2

二级引证文献10

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