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Frizzled receptors in melanomagenesis: From molecular interactions to target identification

Frizzled (FZD) proteins are receptors for the WNT family ligands. Inherited human diseases and genetic experiments using knockout mice have revealed a central role of FZDs in multiple aspects of embryonic development and tissue homeostasis. Misregulated FZD signaling has also been found in many canc...

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Autores principales: Umar, Sheikh A., Dong, Bo, Nihal, Minakshi, Chang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816865/
https://www.ncbi.nlm.nih.gov/pubmed/36620565
http://dx.doi.org/10.3389/fonc.2022.1096134
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author Umar, Sheikh A.
Dong, Bo
Nihal, Minakshi
Chang, Hao
author_facet Umar, Sheikh A.
Dong, Bo
Nihal, Minakshi
Chang, Hao
author_sort Umar, Sheikh A.
collection PubMed
description Frizzled (FZD) proteins are receptors for the WNT family ligands. Inherited human diseases and genetic experiments using knockout mice have revealed a central role of FZDs in multiple aspects of embryonic development and tissue homeostasis. Misregulated FZD signaling has also been found in many cancers. Recent studies on three out of the ten mammalian FZDs in melanoma have shown that they promote tumor cell proliferation and invasion, via the activation of the canonical WNT/β-catenin or non-canonical PCP signaling pathway. In this concise review, we summarize our current knowledge of individual FZDs in melanoma, discuss the involvement of both the canonical and non-canonical pathways, and describe ongoing efforts to target the FZD receptors for melanoma treatment.
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spelling pubmed-98168652023-01-07 Frizzled receptors in melanomagenesis: From molecular interactions to target identification Umar, Sheikh A. Dong, Bo Nihal, Minakshi Chang, Hao Front Oncol Oncology Frizzled (FZD) proteins are receptors for the WNT family ligands. Inherited human diseases and genetic experiments using knockout mice have revealed a central role of FZDs in multiple aspects of embryonic development and tissue homeostasis. Misregulated FZD signaling has also been found in many cancers. Recent studies on three out of the ten mammalian FZDs in melanoma have shown that they promote tumor cell proliferation and invasion, via the activation of the canonical WNT/β-catenin or non-canonical PCP signaling pathway. In this concise review, we summarize our current knowledge of individual FZDs in melanoma, discuss the involvement of both the canonical and non-canonical pathways, and describe ongoing efforts to target the FZD receptors for melanoma treatment. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9816865/ /pubmed/36620565 http://dx.doi.org/10.3389/fonc.2022.1096134 Text en Copyright © 2022 Umar, Dong, Nihal and Chang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Umar, Sheikh A.
Dong, Bo
Nihal, Minakshi
Chang, Hao
Frizzled receptors in melanomagenesis: From molecular interactions to target identification
title Frizzled receptors in melanomagenesis: From molecular interactions to target identification
title_full Frizzled receptors in melanomagenesis: From molecular interactions to target identification
title_fullStr Frizzled receptors in melanomagenesis: From molecular interactions to target identification
title_full_unstemmed Frizzled receptors in melanomagenesis: From molecular interactions to target identification
title_short Frizzled receptors in melanomagenesis: From molecular interactions to target identification
title_sort frizzled receptors in melanomagenesis: from molecular interactions to target identification
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9816865/
https://www.ncbi.nlm.nih.gov/pubmed/36620565
http://dx.doi.org/10.3389/fonc.2022.1096134
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