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Intestinal insulin/IGF1 signalling through FoxO1 regulates epithelial integrity and susceptibility to colon cancer.
Ostermann, A L; Wunderlich, C M; Schneiders, L; Vogt, M C; Woeste, M A; Belgardt, B F; Niessen, C M; Martiny, B; Schauss, A C; Frommolt, P; Nikolaev, A; Hövelmeyer, N; Sears, R C; Koch, P J; Günzel, D; Brüning, J C; Wunderlich, F T.
Afiliação
  • Ostermann AL; Max Planck Institute for Metabolism Research, Cologne, Germany.
  • Wunderlich CM; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Cologne, Germany.
  • Schneiders L; Center for Endocrinology, Diabetes and Preventive Medicine (CEDP), Cologne, Germany.
  • Vogt MC; Max Planck Institute for Metabolism Research, Cologne, Germany.
  • Woeste MA; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Cologne, Germany.
  • Belgardt BF; Center for Endocrinology, Diabetes and Preventive Medicine (CEDP), Cologne, Germany.
  • Niessen CM; Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Martiny B; Max Planck Institute for Metabolism Research, Cologne, Germany.
  • Schauss AC; Max Planck Institute for Metabolism Research, Cologne, Germany.
  • Frommolt P; Max Planck Institute for Metabolism Research, Cologne, Germany.
  • Nikolaev A; Max Planck Institute for Metabolism Research, Cologne, Germany.
  • Hövelmeyer N; German Diabetes Center (DDZ), Düsseldorf, Germany.
  • Sears RC; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Cologne, Germany.
  • Koch PJ; Center for Molecular Medicine Cologne (CMMC), Cologne, Germany.
  • Günzel D; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Cologne, Germany.
  • Brüning JC; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Cologne, Germany.
  • Wunderlich FT; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Cologne, Germany.
Nat Metab ; 1(3): 371-389, 2019 03.
Article em En | MEDLINE | ID: mdl-32694718
ABSTRACT
Obesity promotes the development of insulin resistance and increases the incidence of colitis-associated cancer (CAC), but whether a blunted insulin action specifically in intestinal epithelial cells (IECs) affects CAC is unknown. Here, we show that obesity impairs insulin sensitivity in IECs and that mice with IEC-specific inactivation of the insulin and IGF1 receptors exhibit enhanced CAC development as a consequence of impaired restoration of gut barrier function. Blunted insulin signalling retains the transcription factor FOXO1 in the nucleus to inhibit expression of Dsc3, thereby impairing desmosome formation and epithelial integrity. Both IEC-specific nuclear FoxO1ADA expression and IEC-specific Dsc3 inactivation recapitulate the impaired intestinal integrity and increased CAC burden. Spontaneous colonic tumour formation and compromised intestinal integrity are also observed upon IEC-specific coexpression of FoxO1ADA and a stable Myc variant, thus suggesting a molecular mechanism through which impaired insulin action and nuclear FOXO1 in IECs promotes CAC.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator de Crescimento Insulin-Like I / Neoplasias do Colo / Proteína Forkhead Box O1 / Insulina / Mucosa Intestinal Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator de Crescimento Insulin-Like I / Neoplasias do Colo / Proteína Forkhead Box O1 / Insulina / Mucosa Intestinal Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article