Literature DB >> 28814670

MTG16 is a tumor suppressor in colitis-associated carcinoma.

Elizabeth M McDonough1, Caitlyn W Barrett2, Bobak Parang2, Mukul K Mittal3, J Joshua Smith4, Amber M Bradley3, Yash A Choksi3, Lori A Coburn3,5, Sarah P Short2, Joshua J Thompson2, Baolin Zhang2, Shenika V Poindexter2, Melissa A Fischer6, Xi Chen7, Jiang Li8, Frank L Revetta9, Rishi Naik2,3, M Kay Washington9, Michael J Rosen10, Scott W Hiebert6, Keith T Wilson2,3,5,11, Christopher S Williams2,3,5,11.   

Abstract

MTG16 is a member of the myeloid translocation gene (MTG) family of transcriptional corepressors. While MTGs were originally identified in chromosomal translocations in acute myeloid leukemia, recent studies have uncovered a role in intestinal biology. For example, Mtg16-/- mice have increased intestinal proliferation and are more sensitive to intestinal injury in colitis models. MTG16 is also underexpressed in patients with moderate/severe ulcerative colitis. Based on these findings, we postulated that MTG16 might protect against colitis-associated carcinogenesis. MTG16 was downregulated at the protein and RNA levels in patients with inflammatory bowel disease and in those with colitis-associated carcinoma. Mtg16-/- mice subjected to inflammatory carcinogenesis modeling exhibited worse colitis and increased tumor multiplicity and size. Loss of MTG16 also increased severity of dysplasia, apoptosis, proliferation, DNA damage, and WNT signaling. Moreover, transplantation of WT marrow into Mtg16-/- mice failed to rescue the Mtg16-/- protumorigenic phenotypes, indicating an epithelium-specific role for MTG16. While MTG dysfunction is widely appreciated in hematopoietic malignancies, the role of this gene family in epithelial homeostasis, and in colon cancer, was unrealized. This report identifies MTG16 as an important modulator of colitis and tumor development in inflammatory carcinogenesis.

Entities:  

Keywords:  Gastroenterology; Genetics; Inflammation; Oncology

Year:  2017        PMID: 28814670      PMCID: PMC5621889          DOI: 10.1172/jci.insight.78210

Source DB:  PubMed          Journal:  JCI Insight        ISSN: 2379-3708


  46 in total

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Authors:  Daniel A Sussman; Rebeca Santaolalla; Sebastian Strobel; Rishu Dheer; Maria T Abreu
Journal:  Curr Opin Gastroenterol       Date:  2012-07       Impact factor: 3.287

2.  Dynamic activation of the key pathways: linking colitis to colorectal cancer in a mouse model.

Authors:  Anliu Tang; Nan Li; Xiayu Li; Hongyuan Yang; Wei Wang; Liyang Zhang; Guiyuan Li; Wei Xiong; Jian Ma; Shourong Shen
Journal:  Carcinogenesis       Date:  2012-05-19       Impact factor: 4.944

3.  High resolution colonoscopy in live mice.

Authors:  C Becker; M C Fantini; M F Neurath
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

4.  MTGR1 is required for tumorigenesis in the murine AOM/DSS colitis-associated carcinoma model.

Authors:  Caitlyn W Barrett; Barbara Fingleton; Amanda Williams; Wei Ning; Melissa A Fischer; Mary K Washington; Rupesh Chaturvedi; Keith T Wilson; Scott W Hiebert; Christopher S Williams
Journal:  Cancer Res       Date:  2011-02-08       Impact factor: 12.701

Review 5.  Cancer in inflammatory bowel disease.

Authors:  Jianlin Xie; Steven H Itzkowitz
Journal:  World J Gastroenterol       Date:  2008-01-21       Impact factor: 5.742

6.  Chronic experimental colitis induced by dextran sulphate sodium (DSS) is characterized by Th1 and Th2 cytokines.

Authors:  L A Dieleman; M J Palmen; H Akol; E Bloemena; A S Peña; S G Meuwissen; E P Van Rees
Journal:  Clin Exp Immunol       Date:  1998-12       Impact factor: 4.330

7.  NF-kappaB binds to a polymorphic repressor element in the MMP-3 promoter.

Authors:  Ruth C Borghaei; P Lyle Rawlings; Masoud Javadi; Joanna Woloshin
Journal:  Biochem Biophys Res Commun       Date:  2004-03-26       Impact factor: 3.575

8.  DNA damage induced by chronic inflammation contributes to colon carcinogenesis in mice.

Authors:  Lisiane B Meira; James M Bugni; Stephanie L Green; Chung-Wei Lee; Bo Pang; Diana Borenshtein; Barry H Rickman; Arlin B Rogers; Catherine A Moroski-Erkul; Jose L McFaline; David B Schauer; Peter C Dedon; James G Fox; Leona D Samson
Journal:  J Clin Invest       Date:  2008-07       Impact factor: 14.808

9.  Synergistic upregulation of metalloproteinase-9 by growth factors and inflammatory cytokines: an absolute requirement for transcription factor NF-kappa B.

Authors:  M Bond; R P Fabunmi; A H Baker; A C Newby
Journal:  FEBS Lett       Date:  1998-09-11       Impact factor: 4.124

10.  Differential expression analysis for sequence count data.

Authors:  Simon Anders; Wolfgang Huber
Journal:  Genome Biol       Date:  2010-10-27       Impact factor: 13.583

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  2 in total

1.  MTG16 regulates colonic epithelial differentiation, colitis, and tumorigenesis by repressing E protein transcription factors.

Authors:  Rachel E Brown; Justin Jacobse; Shruti A Anant; Koral M Blunt; Bob Chen; Paige N Vega; Chase T Jones; Jennifer M Pilat; Frank Revetta; Aidan H Gorby; Kristy R Stengel; Yash A Choksi; Kimmo Palin; M Blanca Piazuelo; Mary Kay Washington; Ken S Lau; Jeremy A Goettel; Scott W Hiebert; Sarah P Short; Christopher S Williams
Journal:  JCI Insight       Date:  2022-05-23

2.  The Transcription Co-Repressors MTG8 and MTG16 Regulate Exit of Intestinal Stem Cells From Their Niche and Differentiation Into Enterocyte vs Secretory Lineages.

Authors:  Anna Baulies; Nikolaos Angelis; Valentina Foglizzo; E Thomas Danielsen; Harshil Patel; Laura Novellasdemunt; Anna Kucharska; Joana Carvalho; Emma Nye; Paolo De Coppi; Vivian S W Li
Journal:  Gastroenterology       Date:  2020-06-15       Impact factor: 22.682

  2 in total

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