248
views
0
recommends
+1 Recommend
0 collections
    40
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      STATs in cancer inflammation and immunity: a leading role for STAT3

      , ,
      Nature Reviews Cancer
      Springer Science and Business Media LLC

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Commensurate with their roles in regulating cytokine-dependent inflammation and immunity, signal transducer and activator of transcription (STAT) proteins are central in determining whether immune responses in the tumour microenvironment promote or inhibit cancer. Persistently activated STAT3 and, to some extent, STAT5 increase tumour cell proliferation, survival and invasion while suppressing anti-tumour immunity. The persistent activation of STAT3 also mediates tumour-promoting inflammation. STAT3 has this dual role in tumour inflammation and immunity by promoting pro-oncogenic inflammatory pathways, including nuclear factor-kappaB (NF-kappaB) and interleukin-6 (IL-6)-GP130-Janus kinase (JAK) pathways, and by opposing STAT1- and NF-kappaB-mediated T helper 1 anti-tumour immune responses. Consequently, STAT3 is a promising target to redirect inflammation for cancer therapy.

          Related collections

          Most cited references1

          • Record: found
          • Abstract: not found
          • Book: not found

          Epigenetic Mechanisms of Gene Regulation

            Bookmark

            Author and article information

            Journal
            Nature Reviews Cancer
            Nat Rev Cancer
            Springer Science and Business Media LLC
            1474-175X
            1474-1768
            November 2009
            November 2009
            : 9
            : 11
            : 798-809
            Article
            10.1038/nrc2734
            19851315
            3c92cfa1-def2-48e8-a96b-905a0472fe83
            © 2009

            http://www.springer.com/tdm

            History

            Comments

            Comment on this article