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@article{929226,
author = {FoldynováandTrantírková, S. and Sekyrová, P. and Tmejová, Kateřina and Brumovská, E. and Bernatík, Ondřej and Blankenfeldt, W. and Krejčí, Pavel and Kozubík, Alois and Dolezal, T. and Trantírek, Lukáš and Bryja, Vítězslav},
article_location = {London, Great Britain},
article_number = {12/3},
doi = {http://dx.doi.org/10.1186/bcr2581},
keywords = {KINASE-I-EPSILON; BETA-CATENIN; EPITHELIAL-CELLS; DISHEVELLED PHOSPHORYLATION; REGULATES GASTRULATION; SIGNALING PATHWAY; TUMOR PROGRESSION; UP-REGULATION; WNT PATHWAY; E-CADHERIN},
language = {eng},
issn = {1465-5411},
journal = {Breast Cancer Research},
title = {Breast cancer-specific mutations in CK1epsilon inhibit Wnt/beta-catenin and activate the Wnt/Rac1/JNK and NFAT pathways to decrease cell adhesion and promote cell migration.},
url = {http://www.ncbi.nlm.nih.gov/pubmed/20507565},
volume = {2010},
year = {2010}
}
TY - JOUR
ID - 929226
AU - Foldynová-Trantírková, S. - Sekyrová, P. - Tmejová, Kateřina - Brumovská, E. - Bernatík, Ondřej - Blankenfeldt, W. - Krejčí, Pavel - Kozubík, Alois - Dolezal, T. - Trantírek, Lukáš - Bryja, Vítězslav
PY - 2010
TI - Breast cancer-specific mutations in CK1epsilon inhibit Wnt/beta-catenin and activate the Wnt/Rac1/JNK and NFAT pathways to decrease cell adhesion and promote cell migration.
JF - Breast Cancer Research
VL - 2010
IS - 12/3
SP - 30-31
EP - 30-31
PB - Biomed Central Ltd.
SN - 14655411
KW - KINASE-I-EPSILON
KW - BETA-CATENIN
KW - EPITHELIAL-CELLS
KW - DISHEVELLED PHOSPHORYLATION
KW - REGULATES GASTRULATION
KW - SIGNALING PATHWAY
KW - TUMOR PROGRESSION
KW - UP-REGULATION
KW - WNT PATHWAY
KW - E-CADHERIN
UR - http://www.ncbi.nlm.nih.gov/pubmed/20507565
N2 - Introduction: Breast cancer is one of the most common types of cancer in women. One of the genes that were found mutated in breast cancer is casein kinase 1 epsilon (CK1 epsilon). Because CK1 epsilon is a crucial regulator of the Wnt signaling cascades, we determined how these CK1 epsilon mutations interfere with the Wnt pathway and affect the behavior of epithelial breast cancer cell lines. Results: In silico modeling and in vivo data showed that autophosphorylation at Thr 44, a site adjacent to the breast cancer point mutations in the N-terminal lobe of human CK1 epsilon, is involved in positive regulation of the CK1 epsilon activity. Our data further demonstrate that, in mammalian cells, mutated forms of CK1 epsilon failed to affect the intracellular localization and phosphorylation of Dvl2; we were able to demonstrate that CK1 epsilon mutants were unable to enhance Dvl-induced TCF/LEF-mediated transcription, that CK1 epsilon mutants acted as loss-of-function in the Wnt/beta-catenin pathway, and that CK1 epsilon mutants activated the noncanonical Wnt/Rac-1 and NFAT pathways, similar to pharmacological inhibitors of CK1. In line with these findings, inhibition of CK1 promoted cell migration as well as decreased cell adhesion and E-cadherin expression in the breast cancer-derived cell line MCF7. Conclusions: In summary, these data suggest that the mutations of CK1 epsilon found in breast cancer can suppress Wnt/beta-catenin as well as promote the Wnt/Rac-1/JNK and Wnt/NFAT pathways, thus contributing to breast cancer development via effects on cell adhesion and migration. In terms of molecular mechanism, our data indicate that the breast cancer point mutations in the N-terminal lobe of CK1 epsilon, which are correlated with decreased phosphorylation activities of mutated forms of CK1 epsilon both in vitro and in vivo, interfere with positive autophosphorylation at Thr 44.
ER -
FOLDYNOVÁ-TRANTÍRKOVÁ, S., P. SEKYROVÁ, Kateřina TMEJOVÁ, E. BRUMOVSKÁ, Ondřej BERNATÍK, W. BLANKENFELDT, Pavel KREJČÍ, Alois KOZUBÍK, T. DOLEZAL, Lukáš TRANTÍREK a Vítězslav BRYJA. Breast cancer-specific mutations in CK1epsilon inhibit Wnt/beta-catenin and activate the Wnt/Rac1/JNK and NFAT pathways to decrease cell adhesion and promote cell migration. \textit{Breast Cancer Research}. London, Great Britain: Biomed Central Ltd., roč.~2010, 12/3, s.~30-31. ISSN~1465-5411. doi:10.1186/bcr2581. 2010.
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