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  4. Increase in ADAR1p110 activates the canonical Wnt signaling pathway associated with aggressive phenotype in triple negative breast cancer cells
Details

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
ARMISEN YAÑEZ, RICARDO AMADO  
Facultad de Medicina Clínica Alemana Universidad del Desarrollo  
Type
Resource Types::text::journal::journal article
Scopus ID
2-s2.0-85124163708
WoS ID
WOS:000755542300001
DOI
10.1016/j.gene.2022.146246
URL
https://investigadores.udd.cl/handle/123456789/5229
URL Institutional Repository
http://hdl.handle.net/11447/5869
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
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