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MTG16 is a tumor suppressor in colitis-associated carcinoma.

Authors :
McDonough EM
Barrett CW
Parang B
Mittal MK
Smith JJ
Bradley AM
Choksi YA
Coburn LA
Short SP
Thompson JJ
Zhang B
Poindexter SV
Fischer MA
Chen X
Li J
Revetta FL
Naik R
Washington MK
Rosen MJ
Hiebert SW
Wilson KT
Williams CS
Source :
JCI insight [JCI Insight] 2017 Aug 17; Vol. 2 (16). Date of Electronic Publication: 2017 Aug 17 (Print Publication: 2017).
Publication Year :
2017

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.

Details

Language :
English
ISSN :
2379-3708
Volume :
2
Issue :
16
Database :
MEDLINE
Journal :
JCI insight
Publication Type :
Academic Journal
Accession number :
28814670
Full Text :
https://doi.org/10.1172/jci.insight.78210