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PRDM1 silences stem cell-related genes and inhibits proliferation of human colon tumor organoids.
Liu, Changlong; Banister, Carolyn E; Weige, Charles C; Altomare, Diego; Richardson, Joseph H; Contreras, Carlo M; Buckhaults, Phillip J.
Afiliação
  • Liu C; Department of Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina, Columbia, SC 29208.
  • Banister CE; Department of Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina, Columbia, SC 29208.
  • Weige CC; Department of Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina, Columbia, SC 29208.
  • Altomare D; Department of Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina, Columbia, SC 29208.
  • Richardson JH; Division of Surgical Oncology, Department of Surgery, The University of Alabama at Birmingham, Birmingham, AL 35233.
  • Contreras CM; Division of Surgical Oncology, Department of Surgery, The University of Alabama at Birmingham, Birmingham, AL 35233.
  • Buckhaults PJ; Department of Drug Discovery and Biomedical Sciences, College of Pharmacy, University of South Carolina, Columbia, SC 29208; phillip.buckhaults@gmail.com.
Proc Natl Acad Sci U S A ; 115(22): E5066-E5075, 2018 05 29.
Article em En | MEDLINE | ID: mdl-29760071
ABSTRACT
PRDM1 is a tumor suppressor that plays an important role in B and T cell lymphomas. Our previous studies demonstrated that PRDM1ß is a p53-response gene in human colorectal cancer cells. However, the function of PRDM1ß in colorectal cancer cells and colon tumor organoids is not clear. Here we show that PRDM1ß is a p53-response gene in human colon organoids and that low PRDM1 expression predicts poor survival in colon cancer patients. We engineered PRDM1 knockouts and overexpression clones in RKO cells and characterized the PRDM1-dependent transcript landscapes, revealing that both the α and ß transcript isoforms repress MYC-response genes and stem cell-related genes. Finally, we show that forced expression of PRDM1 in human colon cancer organoids prevents the formation and growth of colon tumor organoids in vitro. These results suggest that p53 may exert tumor-suppressive effects in part through a PRDM1-dependent silencing of stem cell genes, depleting the size of the normal intestinal stem cell compartment in response to DNA damage.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Organoides / Neoplasias do Colo / Proliferação de Células / Fator 1 de Ligação ao Domínio I Regulador Positivo Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Organoides / Neoplasias do Colo / Proliferação de Células / Fator 1 de Ligação ao Domínio I Regulador Positivo Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article