Serine Threonine Kinase 17A Maintains the Epithelial State in Colorectal Cancer Cells.


Journal

Molecular cancer research : MCR
ISSN: 1557-3125
Titre abrégé: Mol Cancer Res
Pays: United States
ID NLM: 101150042

Informations de publication

Date de publication:
04 2019
Historique:
received: 17 09 2018
revised: 27 11 2018
accepted: 08 01 2019
pubmed: 19 1 2019
medline: 10 1 2020
entrez: 19 1 2019
Statut: ppublish

Résumé

Serine threonine kinase 17A (STK17A) is a ubiquitously expressed kinase originally identified as a regulator of apoptosis; however, whether it functionally contributes to colorectal cancer has not been established. Here, we have analyzed STK17A in colorectal cancer and demonstrated decreased expression of STK17A in primary tumors, which is further reduced in metastatic lesions, indicating a potential role in regulating the metastatic cascade. Interestingly, changes in STK17A expression did not modify proliferation, apoptosis, or sensitivity of colorectal cancer cell lines to treatment with the chemotherapeutic 5-fluorouracil. Instead,

Identifiants

pubmed: 30655319
pii: 1541-7786.MCR-18-0990
doi: 10.1158/1541-7786.MCR-18-0990
pmc: PMC6941354
mid: NIHMS1518808
doi:

Substances chimiques

Apoptosis Regulatory Proteins 0
Protein Serine-Threonine Kinases EC 2.7.11.1
STK17A protein, human EC 2.7.11.1
Fluorouracil U3P01618RT

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

882-894

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK099204
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK058404
Pays : United States
Organisme : NIDDK NIH HHS
ID : K08 DK080221
Pays : United States
Organisme : NIDDK NIH HHS
ID : F30 DK111107
Pays : United States
Organisme : BLRD VA
ID : I01 BX001426
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA236733
Pays : United States
Organisme : NIDDK NIH HHS
ID : F32 DK108492
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002243
Pays : United States

Informations de copyright

©2019 American Association for Cancer Research.

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Auteurs

Sarah P Short (SP)

Department of Medicine, Division of Gastroenterology, Vanderbilt University Medical Center, Nashville, Tennessee.
Program in Cancer Biology, Vanderbilt University, Nashville, Tennessee.

Joshua J Thompson (JJ)

Department of Medicine, Division of Gastroenterology, Vanderbilt University Medical Center, Nashville, Tennessee.
Program in Cancer Biology, Vanderbilt University, Nashville, Tennessee.

Anthony J Bilotta (AJ)

Department of Medicine, Division of Gastroenterology, Vanderbilt University Medical Center, Nashville, Tennessee.

Xi Chen (X)

Department of Public Health Sciences and the Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, Florida.

Frank L Revetta (FL)

Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.

M Kay Washington (MK)

Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.

Christopher S Williams (CS)

Department of Medicine, Division of Gastroenterology, Vanderbilt University Medical Center, Nashville, Tennessee. christopher.s.williams@vanderbilt.edu.
Program in Cancer Biology, Vanderbilt University, Nashville, Tennessee.
Veterans Affairs Tennessee Valley Health Care System, Nashville, Tennessee.
Center for Mucosal Inflammation and Cancer, Vanderbilt University Medical Center, Nashville, Tennessee.
Vanderbilt Ingram Cancer Center, Nashville, Tennessee.

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