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Artículo

The signaling pathways activated by ROR1 in cancer

Quezada, Maria JosefinaIcon ; Lopez Bergami, Pablo RobertoIcon
Fecha de publicación: 04/2023
Editorial: Elsevier Science Inc.
Revista: Cellular Signalling
ISSN: 0898-6568
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Otras Ciencias Médicas

Resumen

The receptor tyrosine kinase orphan receptor 1 (ROR1) is a receptor for WNT5A and related Wnt proteins, that play an important role during embryonic development by regulating cell migration, cell polarity, neural patterning, and organogenesis. ROR1 exerts these functions by transducing signals from the Wnt secreted glycoproteins to the intracellular Wnt/PCP and Wnt/Ca++ pathways. Investigations in adult human cells, particularly cancer cells, have demonstrated that besides these two pathways, the WNT5A/ROR1 axis can activate a number of signaling pathways, including the PI3K/AKT, MAPK, NF-κB, STAT3, and Hippo pathways. Moreover, ROR1 is aberrantly expressed in cancer and was associated with tumor progression and poor survival by promoting cell proliferation, survival, invasion, epithelial to mesenchymal transition, and metastasis. Consequently, numerous therapeutic tools to target ROR1 are currently being evaluated in cancer patients. In this review, we will provide a detailed description of the signaling pathways regulated by ROR1 in cancer and their impact in tumor progression.
Palabras clave: AKT , CANCER , MAPK , NF-ΚB , ROR1 , STAT3 , TYROSINE KINASE , WNT5A
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info:eu-repo/semantics/restrictedAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/220075
DOI: http://dx.doi.org/10.1016/j.cellsig.2023.110588
Colecciones
Articulos(SEDE CENTRAL)
Articulos de SEDE CENTRAL
Citación
Quezada, Maria Josefina; Lopez Bergami, Pablo Roberto; The signaling pathways activated by ROR1 in cancer; Elsevier Science Inc.; Cellular Signalling; 104; 4-2023; 1-11
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