干扰素抗肿瘤个性化标记物研究进展

潘驰 黄建瑾

潘驰, 黄建瑾. 干扰素抗肿瘤个性化标记物研究进展[J]. 中国肿瘤临床, 2012, 39(5): 292-295. doi: 10.3969/j.issn.1000-8179.2012.05.012
引用本文: 潘驰, 黄建瑾. 干扰素抗肿瘤个性化标记物研究进展[J]. 中国肿瘤临床, 2012, 39(5): 292-295. doi: 10.3969/j.issn.1000-8179.2012.05.012
Chi PAN, Jianjin HUANG. Advances in Individualized Markers of Interferon in Anti-Cancer Therapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 39(5): 292-295. doi: 10.3969/j.issn.1000-8179.2012.05.012
Citation: Chi PAN, Jianjin HUANG. Advances in Individualized Markers of Interferon in Anti-Cancer Therapy[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2012, 39(5): 292-295. doi: 10.3969/j.issn.1000-8179.2012.05.012

干扰素抗肿瘤个性化标记物研究进展

doi: 10.3969/j.issn.1000-8179.2012.05.012
详细信息
    通讯作者:

    黄建瑾  hhjj@medmail.com.cn

Advances in Individualized Markers of Interferon in Anti-Cancer Therapy

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  • 摘要: 干扰素(interferon, IFN)是具有抗病毒、免疫调节和抗肿瘤等多种生物活性的细胞因子, 可应用于治疗多种肿瘤, 但在肿瘤治疗中的应用剂量往往较大, 因此给患者带来较严重的不良反应, 并且干扰素治疗仅能使部分患者获益。为了提高干扰素治疗的疗效, 并降低其不良反应, 近几年研究主要集中于探索其抗肿瘤机制和个性化标记物。最近研究发现, 许多干扰素相关的基因和蛋白的表达水平不仅与肿瘤发生有关, 还可预测干扰素治疗的敏感性和预后, 如干扰素调节因子(interferon regulatory factor, IRF)、IFNAR2 mRNA、microRNA、IFITM-1等, 其中检测外周血中的标记物极具有临床普及潜力。本文就近几年干扰素抗肿瘤个性化生物标记物的研究进展进行综述。

     

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  • 收稿日期:  2011-06-19
  • 修回日期:  2011-09-29

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