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化学进展 2016, Vol. 28 Issue (7): 1099-1111 DOI: 10.7536/PC151219 前一篇   后一篇

• 综述与评论 •

小分子IL-6/STAT3信号通路抑制剂

叶霁青, 岳晓虹, 孙丽萍*   

  1. 中国药科大学药学院药物化学教研室 江苏省药物分子设计与成药性优化重点实验室 南京 210009
  • 收稿日期:2015-12-01 修回日期:2016-03-01 出版日期:2016-07-15 发布日期:2016-05-17
  • 通讯作者: 孙丽萍 E-mail:chslp@cpu.edu.cn
  • 基金资助:
    国家十二五科技支撑计划重大项目(No.2012BAJ25B04)资助

Small Molecule Inhibitors of IL-6/STAT3 Signaling

Ye Jiqing, Yue Xiaohong, Sun Liping*   

  1. Jiangsu Key Laboratory of Drug Design & Optimization, Department of Medicinal Chemistry, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China
  • Received:2015-12-01 Revised:2016-03-01 Online:2016-07-15 Published:2016-05-17
  • Supported by:
    The work was supported by the National Key Technology R&D Program (No.2012BAJ25B04).
IL-6是细胞内广泛存在的一种细胞因子,参与细胞内大量的生物应答。研究表明所有IL-6家族的细胞因子均能激活STAT3蛋白,同时,STAT3被认为是介导IL-6功能的主要因子。IL-6与其受体结合,激活JAKs,从而使STAT3磷酸化激活,活化的STAT3二聚化,向细胞核内转移并与其靶基因特定位点结合从而调节基因的转录活性。大量的证据表明细胞中异常活化的STAT3在肿瘤生成与恶性转化中具有重要作用。研究显示STAT3蛋白也是抗肿瘤药物设计的有效靶点。到目前为止,多种药物设计方法,如基于结构的虚拟筛选、高通量筛选、基于片段的药物设计等被用于STAT3抑制剂的筛选以及设计;文献也已经报道了许多具有抗肿瘤活性的STAT3抑制剂。本文主要介绍了近年来小分子IL-6/STAT3信号通路抑制剂,尤其是作用于STAT3蛋白的小分子抑制剂的研究进展。
IL-6 is a widespread cytokine which participates in many biological responses. All members of the IL-6 cytokine family are able to activate STAT3, and STAT3 is also recognized as the main mediator of IL-6 functions. IL-6 binding to cell surface receptors results in the activation of the Janus kinases(JAKs) which cause STAT3 phosphorylated. Then activated STAT3 dimerizes translocates to the nucleus and combines with target genes with specific sites, then activats DNA transcriptional activity. Studies show that the abnormally activated STAT3 in cells plays an important role in tumorigenesis and malignant transformation. Meanwhile, STAT3 is a valid target for novel anticancer drug design. So far, many methods, such as structure-based virtual screening, high throughput screening, fragment-based drug design, have been used to screen and design novel STAT3 inhibitors, and thus several classes of small molecule compounds have been identified as STAT3 inhibitors. In this review, we mainly focus on the small molecule IL-6/STAT3 inhibitors especially target STAT3 protein which have been optimized and identified since 2013.

Contents
1 Introduction
2 Small molecule inhibitors of IL-6/STAT3 signaling pathway
2.1 1,4-Naphthoquinones
2.2 Quinolines
2.3 Derivatives of benzo[b]thiophene-1,1-dioxide
2.4 Derivatives of Niclosamide
2.5 Derivatives of salicylic acid
2.6 6-Aminobenzo[d]thiazole-2-thiols
2.7 Tetrahydropyridinepyrazoles
2.8 Flavonoids
2.9 Coumarins
2.10 Metal-containing compounds
2.11 Other small molecule IL-6/STAT3 inhibitors
3 Conclusion

中图分类号: 

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摘要

小分子IL-6/STAT3信号通路抑制剂