Increase in ADAR1p110 activates the canonical Wnt signaling pathway associated with aggressive phenotype in triple negative breast cancer cells
Journal
Gene
ISSN
0378-1119
Date Issued
2022
Author(s)
Fernanda Morales
Paola Pérez
Julio C. Tapia
Lorena Lobos-González
José Manuel Herranz
Francisca Guevara
Pamela Rojas de Santiago
Esteban Palacios
Rodrigo Andaur
Eduardo A. Sagredo
Katherine Marcelain
Type
Resource Types::text::journal::journal article
URL Institutional Repository
Cite this document
Morales, F., Pérez, P., Tapia, J. C., Lobos-González, L., Herranz, J. M., Guevara, F., De Santiago, P. R., Palacios, E., Andaur, R., Sagredo, E. A., Marcelain, K., & Armisén, R. (2022). Increase in ADAR1p110 activates the canonical Wnt signaling pathway associated with aggressive phenotype in triple negative breast cancer cells. Gene, 819, 146246. https://doi.org/10.1016/j.gene.2022.146246
Subjects
adar1
;
tnbc
;
canonical wnt pathway
;
cell invasion
;
breast cancer
;
adenosine deaminase
;
animals
;
beta catenin
;
cell line, tumor
;
cell movement
;
female
;
gene expression regulation, neoplastic
;
glycogen synthase kinase 3 beta
;
humans
;
mice
;
mice, inbred balb c
;
phenotype
;
rna-binding proteins
;
triple negative breast neoplasms
;
wnt signaling pathway
;
adar1 protein
;
adenosine deaminase
;
baculoviral iap repeat containing protein 5
;
beta catenin
;
glycogen synthase kinase 3beta
;
platelet endothelial cell adhesion molecule 1
;
unclassified drug
;
wnt protein
;
adar protein, human
;
adenosine deaminase
;
beta catenin
;
glycogen synthase kinase 3beta
;
rna binding protein
;
animal experiment
;
animal model
;
animal tissue
;
article
;
cancer growth
;
canonical wnt signaling
;
cell invasion assay
;
controlled study
;
human
;
human cell
;
immunohistochemistry
;
in vitro study
;
in vivo study
;
luciferase assay
;
mda-mb-231 cell line
;
mouse
;
nonhuman
;
phenotype
;
protein determination
;
protein expression
;
protein function
;
protein protein interaction
;
triple negative breast cancer
;
tumor vascularization
;
upregulation
;
vascular endothelial cell
;
western blotting
;
animal
;
bagg albino mouse
;
cell motion
;
female
;
gene expression regulation
;
genetics
;
metabolism
;
phenotype
;
triple negative breast cancer
;
tumor cell line
;
wnt signaling