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Artículo

Cellular and molecular mechanisms implicated in the dual role of ROR2 in cancer

Castro, María VictoriaIcon ; Lopez Bergami, Pablo RobertoIcon
Fecha de publicación: 02/2022
Editorial: Elsevier Science Inc.
Revista: Critical Reviews In Oncology Hematology
ISSN: 1040-8428
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Otras Ciencias Médicas

Resumen

ROR1 and ROR2 are Wnt receptors that are critical for β-catenin-independent Wnt pathways and have been linked to processes driving tumor progression, such as cell proliferation, survival, invasion, and therapy resistance. Both receptors have garnered interest as potential therapeutic targets since they are largely absent in adult tissue, are overexpressed in several cancers, and, as members of the receptor tyrosine kinase family, are easier to target than all other components of the pathway. Unlike ROR1 which always promotes tumorigenesis, ROR2 has a very complex role in cancer acting either to promote or inhibit tumor progression in different tumor types. In the present article, we summarize the findings on ROR2 expression in cancer patients and its impact on clinical outcome. Further, we review the biological processes and signaling pathways regulated by ROR2 that explain its dual role in cancer. Finally, we describe the ongoing strategies to target ROR2 in cancer.
Palabras clave: CANCER , ONCOGENE , ROR2 , TUMOR-SUPPRESSOR GENE
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info:eu-repo/semantics/restrictedAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Atribución-NoComercial-SinDerivadas 2.5 Argentina (CC BY-NC-ND 2.5 AR)
Identificadores
URI: http://hdl.handle.net/11336/187051
URL: https://www.sciencedirect.com/science/article/pii/S1040842822000191
DOI: http://dx.doi.org/10.1016/j.critrevonc.2022.103595
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Citación
Castro, María Victoria; Lopez Bergami, Pablo Roberto; Cellular and molecular mechanisms implicated in the dual role of ROR2 in cancer; Elsevier Science Inc.; Critical Reviews In Oncology Hematology; 170; 103595; 2-2022; 1-12
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