Engrailed‐1 Promotes Pancreatic Cancer Metastasis

Author:

Xu Jihao12,Roe Jae‐Seok34,Lee EunJung145,Tonelli Claudia45,Ji Keely Y.1,Younis Omar W.1,Somervile Tim D.D.4,Yao Melissa45,Milazzo Joseph P.4,Tiriac Herve45,Kolarzyk Anna M.6,Lee Esak6,Grem Jean L.7,Lazenby Audrey J.7,Grunkemeyer James A.7,Hollingsworth Michael A.7,Grandgenett Paul M.7,Borowsky Alexander D.8,Park Youngkyu45,Vakoc Christopher R.4,Tuveson David A.45,Hwang Chang‐Il12ORCID

Affiliation:

1. Department of Microbiology and Molecular Genetics University of California Davis Davis CA 95616 USA

2. Comprehensive Cancer Center University of California Davis Sacramento CA 95817 USA

3. Department of Biochemistry Yonsei University Seoul 03722 South Korea

4. Cold Spring Harbor Laboratory Cold Spring Harbor NY 11724 USA

5. Lustgarten Foundation Pancreatic Cancer Research Laboratory Cold Spring Harbor NY 11724 USA

6. Nancy E. and Peter C. Meinig School of Biomedical Engineering Cornell University Ithaca NY 14853 USA

7. Department of Medicine University of Nebraska Medical Center Omaha NE 68198 USA

8. Department of Pathology School of Medicine University of California Davis Sacramento CA 95817 USA

Abstract

AbstractEngrailed‐1 (EN1) is a critical homeodomain transcription factor (TF) required for neuronal survival, and EN1 expression has been shown to promote aggressive forms of triple negative breast cancer. Here, it is reported that EN1 is aberrantly expressed in a subset of pancreatic ductal adenocarcinoma (PDA) patients with poor outcomes. EN1 predominantly repressed its target genes through direct binding to gene enhancers and promoters, implicating roles in the activation of MAPK pathways and the acquisition of mesenchymal cell properties. Gain‐ and loss‐of‐function experiments demonstrated that EN1 promoted PDA transformation and metastasis in vitro and in vivo. The findings nominate the targeting of EN1 and downstream pathways in aggressive PDA.

Funder

National Research Foundation of Korea

National Institutes of Health

Simons Foundation

National Institute of Environmental Health Sciences

National Cancer Institute

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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