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      TGF-beta suppresses tumor progression in colon cancer by inhibition of IL-6 trans-signaling.

      Immunity
      Animals, Blotting, Western, Colonic Neoplasms, immunology, metabolism, pathology, DNA-Binding Proteins, Disease Models, Animal, Disease Progression, Endoscopy, Digestive System, Enzyme-Linked Immunosorbent Assay, Humans, Immunohistochemistry, Interleukin-6, Intestinal Mucosa, Mice, Mice, Knockout, Mice, Transgenic, Protein-Serine-Threonine Kinases, Receptors, Interleukin-6, Receptors, Transforming Growth Factor beta, genetics, Recombinant Fusion Proteins, Reverse Transcriptase Polymerase Chain Reaction, STAT3 Transcription Factor, Signal Transduction, physiology, T-Lymphocytes, Trans-Activators, Transforming Growth Factor beta

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          Abstract

          Alterations of TGF-beta signaling have been described in colorectal cancer, although the molecular consequences are largely unknown. By using transgenic mice overexpressing TGF-beta or a dominant-negative TGF-betaRII, we demonstrate that TGF-beta signaling in tumor infiltrating T lymphocytes controls the growth of dysplastic epithelial cells in experimental colorectal cancer, as determined by histology and a novel system for high-resolution chromoendoscopy. At the molecular level, TGF-beta signaling in T cells regulated STAT-3 activation in tumor cells via IL-6. IL-6 signaling required tumor cell-derived soluble IL-6R rather than membrane bound IL-6R and suppression of such TGF-beta-dependent IL-6 trans-signaling prevented tumor progression in vivo. Taken together, our data provide novel insights into TGF-beta signaling in colorectal cancer and suggest novel therapeutic approaches for colorectal cancer based on inhibition of TGF-beta-dependent IL-6 trans-signaling.

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