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Engrailed-1 Promotes Pancreatic Cancer Metastasis
被引:2
|作者:
Xu, Jihao
[1
,2
]
Roe, Jae-Seok
[3
,4
]
Lee, Eunjung
[1
,4
,5
]
Tonelli, Claudia
[4
,5
]
Ji, Keely Y.
[1
]
Younis, Omar W.
[1
]
Somervile, Tim D. D.
[4
]
Yao, Melissa
[4
,5
]
Milazzo, Joseph P.
[4
]
Tiriac, Herve
[4
,5
]
Kolarzyk, Anna M.
[6
]
Lee, Esak
[6
]
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, Youngkyu
[4
,5
]
Vakoc, Christopher R.
[4
]
Tuveson, David A.
[4
,5
]
Hwang, Chang-Il
[1
,2
]
机构:
[1] Univ Calif Davis, Dept Microbiol & Mol Genet, Davis, CA 95616 USA
[2] Univ Calif Davis, Comprehens Canc Ctr, Sacramento, CA 95817 USA
[3] Yonsei Univ, Dept Biochem, Seoul 03722, South Korea
[4] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[5] Lustgarten Fdn Pancreat Canc Res Lab, Cold Spring Harbor, NY 11724 USA
[6] Cornell Univ, Nancy E & Peter C Meinig Sch Biomed Engn, Ithaca, NY 14853 USA
[7] Univ Nebraska Med Ctr, Dept Med, Omaha, NE 68198 USA
[8] Univ Calif Davis, Sch Med, Dept Pathol, Sacramento, CA 95817 USA
基金:
新加坡国家研究基金会;
关键词:
apoptosis;
cancer progression;
cancer therapeutics;
developmental transcription factor;
Engrailed-1;
epigenetic reprogramming;
ERK signaling;
metastasis;
pancreatic ductal adenocarcinoma;
MIDBRAIN DOPAMINERGIC-NEURONS;
CELL FATE;
PROGRESSION;
GENES;
TUMOR;
SENSITIVITY;
ANNOTATION;
EXPRESSION;
SUBTYPES;
SURVIVAL;
D O I:
10.1002/advs.202308537
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Engrailed-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. Metastatic pancreatic cancer exhibits aberrant expression of EN1, a critical homeodomain transcription factor for neuronal survival. EN1 predominantly represses its target genes by directly binding to their enhancers and promoters, implicating involvement in MAPK pathways and mesenchymal cell properties. Targeting EN1 and associated pathways may represent a promising strategy to exploit vulnerabilities in aggressive pancreatic cancer.image
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页数:18
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