FRA1 promotes squamous cell carcinoma growth and metastasis through distinct AKT and c-Jun dependent mechanisms.

dc.contributor.author

Zhang, Xiaoling

dc.contributor.author

Wu, Joseph

dc.contributor.author

Luo, Suju

dc.contributor.author

Lechler, Terry

dc.contributor.author

Zhang, Jennifer Y

dc.coverage.spatial

United States

dc.date.accessioned

2017-08-02T13:54:57Z

dc.date.available

2017-08-02T13:54:57Z

dc.date.issued

2016-06-07

dc.description.abstract

FRA1 (Fos-like antigen 1) is highly expressed in many epithelial cancers including squamous cell carcinoma of the skin (cSCC) and head and neck (HNSCC). However, the functional importance and the mechanisms mediating FRA1 function in these cancers are not fully understood. Here, we demonstrate that FRA1 gene silencing in HNSCC and cSCC cells resulted in two consequences - impaired cell proliferation and migration. FRA1 regulation of cell growth was distinct from that of c-Jun, a prominent Jun group AP-1 factor. While c-Jun was required for the expression of the G1/S phase cell cycle promoter CDK4, FRA1 was essential for AKT activation and AKT-dependent expression of CyclinB1, a molecule required for G2-M progression. Exogenous expression of a constitutively active form of AKT rescued cancer cell growth defect caused by FRA1-loss. Additionally, FRA1 knockdown markedly slowed cell adhesion and migration, and conversely expression of an active FRA1 mutant (FRA1DD) expedited these processes in a JNK/c-Jun-dependent manner. Through protein and ChIP-PCR analyses, we identified KIND1, a cytoskeletal regulator of the cell adhesion molecule β1-integrin, as a novel FRA1 transcriptional target. Restoring KIND1 expression rescued migratory defects induced by FRA1 loss. In agreement with these in vitro data, HNSCC cells with FRA1 loss displayed markedly reduced rates of subcutaneous tumor growth and pulmonary metastasis. Together, these results indicate that FRA1 promotes cancer growth through AKT, and enhances cancer cell migration through JNK/c-Jun, pinpointing FRA1 as a key integrator of JNK and AKT signaling pathways and a potential therapeutic target for cSCC and HNSCC.

dc.identifier

https://www.ncbi.nlm.nih.gov/pubmed/27144339

dc.identifier

9110

dc.identifier.eissn

1949-2553

dc.identifier.uri

https://hdl.handle.net/10161/15165

dc.language

eng

dc.publisher

Impact Journals, LLC

dc.relation.ispartof

Oncotarget

dc.relation.isversionof

10.18632/oncotarget.9110

dc.subject

AKT

dc.subject

FRA1

dc.subject

SCC

dc.subject

c-Jun

dc.subject

cyclinB1

dc.title

FRA1 promotes squamous cell carcinoma growth and metastasis through distinct AKT and c-Jun dependent mechanisms.

dc.type

Journal article

duke.contributor.orcid

Zhang, Jennifer Y|0000-0002-4485-1750

pubs.author-url

https://www.ncbi.nlm.nih.gov/pubmed/27144339

pubs.begin-page

34371

pubs.end-page

34383

pubs.issue

23

pubs.organisational-group

Basic Science Departments

pubs.organisational-group

Cell Biology

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Dermatology

pubs.organisational-group

Duke

pubs.organisational-group

Duke Cancer Institute

pubs.organisational-group

Institutes and Centers

pubs.organisational-group

Pathology

pubs.organisational-group

School of Medicine

pubs.publication-status

Published

pubs.volume

7

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
FRA1 promotes squamous cell carcinoma growth and metastasis through distinct AKT and c-Jun dependent mechanisms.pdf
Size:
7.61 MB
Format:
Adobe Portable Document Format
Description:
Published version