Author
Listed:
- Shan Wang
(State Key Laboratories for Agrobiotechnology, College of Biological Sciences, China Agricultural University
School of Veterinary Medicine, University of Pennsylvania)
- Ning Li
(School of Veterinary Medicine, University of Pennsylvania)
- Maryam Yousefi
(School of Veterinary Medicine, University of Pennsylvania
Cell and Molecular Biology Graduate Program, University of Pennsylvania)
- Angela Nakauka-Ddamba
(School of Veterinary Medicine, University of Pennsylvania)
- Fan Li
(School of Arts and Sciences, University of Pennsylvania
PENN Genome Frontiers Institute, University of Pennsylvania
Genomics and Computational Biology Graduate Program, University of Pennsylvania)
- Kimberly Parada
(School of Veterinary Medicine, University of Pennsylvania)
- Shilpa Rao
(PENN Molecular Profiling Facility, University of Pennsylvania)
- Gerard Minuesa
(Molecular Pharmacology and Chemistry Program, Experimental Therapeutics Center and Center for Stem Cell Biology, Memorial Sloan-Kettering Cancer Center)
- Yarden Katz
(The Broad Institute of Harvard and MIT)
- Brian D. Gregory
(School of Arts and Sciences, University of Pennsylvania
PENN Genome Frontiers Institute, University of Pennsylvania
Genomics and Computational Biology Graduate Program, University of Pennsylvania)
- Michael G. Kharas
(Molecular Pharmacology and Chemistry Program, Experimental Therapeutics Center and Center for Stem Cell Biology, Memorial Sloan-Kettering Cancer Center)
- Zhengquan Yu
(State Key Laboratories for Agrobiotechnology, College of Biological Sciences, China Agricultural University)
- Christopher J. Lengner
(School of Veterinary Medicine, University of Pennsylvania
Cell and Molecular Biology Graduate Program, University of Pennsylvania
Center for Molecular Studies in Digestive and Liver Diseases, University of Pennsylvania
School of Medicine, University of Pennsylvania)
Abstract
The MSI2 RNA-binding protein is a potent oncogene playing key roles in haematopoietic stem cell homeostasis and malignant haematopoiesis. Here we demonstrate that MSI2 is expressed in the intestinal stem cell compartment, that its expression is elevated in colorectal adenocarcinomas, and that MSI2 loss-of-function abrogates colorectal cancer cell growth. MSI2 gain-of-function in the intestinal epithelium in a drug-inducible mouse model is sufficient to phenocopy many of the morphological and molecular consequences of acute loss of the APC tumour suppressor in the intestinal epithelium in a Wnt-independent manner. Transcriptome-wide RNA-binding analysis indicates that MSI2 acts as a pleiotropic inhibitor of known intestinal tumour suppressors including Lrig1, Bmpr1a, Cdkn1a and Pten. Finally, we demonstrate that inhibition of the PDK–AKT–mTORC1 axis rescues oncogenic consequences of MSI2 induction. Taken together, our findings identify MSI2 as a central component in an unappreciated oncogenic pathway promoting intestinal transformation.
Suggested Citation
Shan Wang & Ning Li & Maryam Yousefi & Angela Nakauka-Ddamba & Fan Li & Kimberly Parada & Shilpa Rao & Gerard Minuesa & Yarden Katz & Brian D. Gregory & Michael G. Kharas & Zhengquan Yu & Christopher , 2015.
"Transformation of the intestinal epithelium by the MSI2 RNA-binding protein,"
Nature Communications, Nature, vol. 6(1), pages 1-15, May.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7517
DOI: 10.1038/ncomms7517
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Cited by:
- Joana Silva & Ferhat Alkan & Sofia Ramalho & Goda Snieckute & Stefan Prekovic & Ana Krotenberg Garcia & Santiago Hernández-Pérez & Rob Kammen & Danielle Barnum & Liesbeth Hoekman & Maarten Altelaar & , 2022.
"Ribosome impairment regulates intestinal stem cell identity via ZAKɑ activation,"
Nature Communications, Nature, vol. 13(1), pages 1-12, December.
- Bin Zhang & Dandan Zhao & Fang Chen & David Frankhouser & Huafeng Wang & Khyatiben V. Pathak & Lei Dong & Anakaren Torres & Krystine Garcia-Mansfield & Yi Zhang & Dinh Hoa Hoang & Min-Hsuan Chen & Shu, 2023.
"Acquired miR-142 deficit in leukemic stem cells suffices to drive chronic myeloid leukemia into blast crisis,"
Nature Communications, Nature, vol. 14(1), pages 1-21, December.
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