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Interleukin-6 promotes tumor progression in colitis-associated colorectal cancer through HIF-1 alpha regulation  期刊论文  

  • 编号:
    1c9f06d6-d4d8-4073-82b1-cc9674494e81
  • 作者:
  • 语种:
    English
  • 期刊:
    ONCOLOGY LETTERS ISSN:1792-1074 2016 年 12 卷 6 期 (4665 - 4670) ; DEC
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  • 关键词:
  • 摘要:

    Interleukin-6 (IL-6) is a well-known etiological factor of colitis-associated colorectal cancer (CAC) and has a significant role in CAC progression. In addition, hypoxia-inducible factor 1 alpha (HIF-1 alpha) serves a primary role in the progression of CAC. However, the association between IL-6 and HIF-1 alpha during the progression of CAC remains unclear. To investigate this association, the present study induced CAC in a mouse model using azoxymethane and dextran sulfate sodium. In addition, an anti-IL-6 receptor antibody was used to inhibit IL-6. In this model, anti-IL-6 receptor antibody treatment significantly inhibited the development of CAC and the expression of HIF-1 alpha, in colorectal adenomas and adenocarcinomas. In patients with CAC, the HIF-1 alpha gene was demonstrated to be overexpressed in tumor tissue compared with adjacent non-malignant tissue. Furthermore, HIF-1 alpha mRNA expression was positively correlated with serum IL-6 concentration. The results of the present study suggest that IL-6 promotes CAC progression, in the early stage of the disease, through HIF-1 alpha regulation.

  • 推荐引用方式
    GB/T 7714:
    Han Jun,Xi Qiulei,Meng Qingyang, et al. Interleukin-6 promotes tumor progression in colitis-associated colorectal cancer through HIF-1 alpha regulation [J].ONCOLOGY LETTERS,2016,12(6):4665-4670.
  • APA:
    Han Jun,Xi Qiulei,Meng Qingyang,Liu Jingzheng,&Wu Guohao.(2016).Interleukin-6 promotes tumor progression in colitis-associated colorectal cancer through HIF-1 alpha regulation .ONCOLOGY LETTERS,12(6):4665-4670.
  • MLA:
    Han Jun, et al. "Interleukin-6 promotes tumor progression in colitis-associated colorectal cancer through HIF-1 alpha regulation" .ONCOLOGY LETTERS 12,6(2016):4665-4670.
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