A variant of Smurf2 protects mice against colitis-associated colon cancer by inducing transforming growth factor β signaling
| Autor: | Christoph Becker, Clemens Neufert, Susanne Rosfa, Jürgen Siebler, Heike Dornhoff, Dennis Strand, Stefan Tenzer, Jürgen Markl, Jonas Mudter, Markus F. Neurath, Stefan Wirtz |
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| Rok vydání: | 2011 |
| Předmět: |
Colorectal cancer
medicine.medical_treatment Lymphocyte Ubiquitin-Protein Ligases SMAD Biology Proinflammatory cytokine Receptors G-Protein-Coupled chemistry.chemical_compound Mice Transforming Growth Factor beta medicine Animals Cells Cultured Hepatology Azoxymethane Gene Expression Profiling Gastroenterology medicine.disease Colitis Molecular biology Ubiquitin ligase Mice Inbred C57BL Proto-Oncogene Proteins c-kit Cytokine medicine.anatomical_structure Hyaluronan Receptors chemistry Colonic Neoplasms biology.protein Cancer research Transforming growth factor Signal Transduction |
| Zdroj: | Gastroenterology. 142(5) |
| ISSN: | 1528-0012 |
| Popis: | Background & Aims Transforming growth factor (TGF)-β signaling, which is down-regulated by the E3 ubiquitin ligase Smad ubiquitin regulating factor 2 (Smurf2), promotes development of cancer. We identified a splice variant of Smurf2 (ΔE2Smurf2) and investigated its role in colon carcinogenesis in mice. Methods Colitis-associated colon cancer was induced in mice by administration of azoxymethane, followed by 3 cycles of oral administration of dextran sodium sulfate. Messenger RNA levels of Smurf2 in colon tumors and control tissue were measured by quantitative polymerase chain reaction; lymphocyte and cytokine levels were measured in tumor and tissue samples. Results Tumor-infiltrating CD4 + cells expressed higher levels of ΔE2Smurf2 than CD4 + cells from nontumor tissues of wild-type mice. T cell–specific overexpression of ΔE2Smurf2 increased TGF-β signaling by suppressing protein levels of Smurf2, accompanied by an increase in levels of TGF-β receptor type II. Transgenic mice that overexpress ΔE2Smurf2 were protected against development of colitis-associated tumors and down-regulated proinflammatory cytokines such as interleukin-6. Patients with chronic inflammatory bowel disease had a significantly lower ratio of Smurf2/ΔE2Smurf2 than control individuals. Conclusions T cell–specific ΔE2Smurf2 degrades wild-type Smurf2 and controls intestinal tumor growth in mice by up-regulating TGF-β receptor type II, reducing proliferation and production of proinflammatory cytokines. |
| Databáze: | OpenAIRE |
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