癌变·畸变·突变 ›› 2019, Vol. 31 ›› Issue (4): 295-299.doi: 10.3969/j.issn.1004-616x.2019.04.006

• 论著 • 上一篇    下一篇

白细胞介素-17过表达胃癌细胞在小鼠体内的成瘤效应研究

张智萍1,3, 单保恩1, 宋静静1, 王浩1, 刘英姿1, 陈伟1, 高立平1, 李巧霞2   

  1. 1. 河北医科大学第四医院科研中心, 河北 石家庄 050011;
    2. 河北医科大学第四医院临床生物细胞室, 河北 石家庄 050011;
    3. 河北医科大学第二医院特检科, 河北 石家庄 050011
  • 收稿日期:2018-09-20 修回日期:2019-01-08 出版日期:2019-07-30 发布日期:2019-08-23
  • 通讯作者: 李巧霞,E-mail:759767368@qq.com E-mail:759767368@qq.com
  • 作者简介:张智萍,E-mail:550539269@qq.com。
  • 基金资助:
    河北省自然科学基金(H2016206209);河北省人才工程培养经费项目(A201401251);河北省政府资助临床医学优秀人才项目

Tumorigenic effect of interleukin?17 overexpressing gastric cells in mice

ZHANG Zhiping1,3, SHAN Baoen1, SONG Jingjing1, WANG Hao1, LIU Yingzi1, CHEN Wei1, GAO Liping1, LI Qiaoxia2   

  1. 1. Research Centre of the Fourth Hospital of Hebei Medical University, Shijiazhuang 050011;
    2. The Clinical Biological Cell Room of the Fourth Hospital of Hebei Medical University, Shijiazhuang 050011;
    3. Exceptional Laboratory Department of the Second Hospital of Hebei Medical University, Shijiazhuang 050011, Hebei, China
  • Received:2018-09-20 Revised:2019-01-08 Online:2019-07-30 Published:2019-08-23

摘要: 目的:建立小鼠荷瘤模型,研究白细胞介素-17(IL-17)过表达的胃癌细胞在小鼠体内的成瘤效应。方法:分别以MFC、MFC/pcDNA3.1和MFC/IL-17细胞接种615小鼠,细胞浓度为5×106个/mL,按每只200 μL注射于小鼠背部皮下。每组10只,观察小鼠皮下肿瘤生长情况。3周后处死小鼠,分别采用RT-PCR和Western blot法检测肿瘤组织内IL-17、VEGF、Podoplanin mRNA和蛋白表达;免疫组化法检测微血管密度。结果:MFC/IL-17组小鼠于接种后5~7 d开始形成肿瘤结节,且生长迅速,肿瘤质量为(5.384±0.391)g,大于MFC组[(1.726±0.445)g]和MFC/pcDNA3.1组[(2.064±0.397)g](P < 0.05)。RT-PCR和Western blot结果显示,与MFC和MFC/pcDNA3.1组相比,MFC/IL-17组小鼠肿瘤组织内IL-17、VEGF、Podoplanin mRNA和蛋白表达均明显增加(P < 0.05)。免疫组化结果显示,与MFC和MFC/pcDNA3.1组相比,MFC/IL-17组小鼠肿瘤组织内微血管密度明显增加(P < 0.05)。结论:IL-17可能通过上调VEGF、Podoplanin和CD31的表达促进血管和淋巴管形成,加速肿瘤生长。

关键词: IL-17, 胃癌细胞, 血管形成, 促肿瘤作用

Abstract: OBJECTIVE:The aim was to investigate tumorigenic effects of interleukin-17 (IL-17) overexpressing gastric cancer cells in mice. METHODS:MFC,MFC/pcDNA3.1 and MFC/IL-17 cells were inoculated subcutaneously into 615 mice,with 10 mice in each group. Three weeks after the inoculation when tumors became obvious,mRNA and protein expressions of IL-17,vascular endothelial growth factor (VEGF) and Podoplanin in tumor tissues were detected using RT-PCR and Western-blots. Micro-vessel density was detected by immunohistochemistry. RESULTS:Tumor nodules developed on 5-7 d after inoculation and grew rapidly in mice inoculated with MFC/IL-17 (MFC/IL-17 mice). The average tumor weights in MFC/IL-17 mice[(5.384±0.391) g] were significantly more than that in MFC mice[(1.726±0.445) g] and MFC/pcDNA3.1 mice[(2.064±0.397) g] (P < 0.05). In addition,the mRNA and protein expressions of IL-17,VEGF and Podoplanin in MFC/IL-17 mice were significantly higher than that in MFC and MFC/pcDNA3.1 mice (P < 0.05). The micro-vessel densities were significantly increased in MFC/IL-17 mice than that in MFC and MFC/pcDNA3.1 mice (P < 0.05). CONCLUSION:Our data show that expression of IL-17 accelerated tumor growth in vivo by up-regulating the expression of VEGF,Podoplanin and CD31,thus promoting angiogenesis and lymphatic vessel formation.

Key words: IL-17, gastric cancer cells, angiogenesis, tumor-promoting effect

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