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Fascin in Cell Migration: More Than an Actin Bundling Protein

SIMPLE SUMMARY: Cell migration is an essential biological process that regulates both development and diseases, such as cancer metastasis. Therefore, understanding the factors that promote cell migration is crucial. One of the factors known to regulate cell migration is the actin-binding protein, Fa...

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Autores principales: Lamb, Maureen C., Tootle, Tina L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698196/
https://www.ncbi.nlm.nih.gov/pubmed/33212856
http://dx.doi.org/10.3390/biology9110403
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author Lamb, Maureen C.
Tootle, Tina L.
author_facet Lamb, Maureen C.
Tootle, Tina L.
author_sort Lamb, Maureen C.
collection PubMed
description SIMPLE SUMMARY: Cell migration is an essential biological process that regulates both development and diseases, such as cancer metastasis. Therefore, understanding the factors that promote cell migration is crucial. One of the factors known to regulate cell migration is the actin-binding protein, Fascin. Fascin is typically thought to promote cell migration through bundling actin to form migratory structures such as filopodia and invadapodia. However, Fascin has many other functions in the cell that may contribute to cell migration. How these novel functions promote cell migration and are regulated is still not well understood. Here, we review the structure of Fascin, the many functions of Fascin and how they may promote cell migration, how Fascin is regulated, and Fascin’s role in diseases such as cancer metastasis. ABSTRACT: Fascin, an actin-binding protein, regulates many developmental migrations and contributes to cancer metastasis. Specifically, Fascin promotes cell motility, invasion, and adhesion by forming filopodia and invadopodia through its canonical actin bundling function. In addition to bundling actin, Fascin has non-canonical roles in the cell that are thought to promote cell migration. These non-canonical functions include regulating the activity of other actin-binding proteins, binding to and regulating microtubules, mediating mechanotransduction to the nucleus via interaction with the Linker of the Nucleoskeleton and Cytoskeleton (LINC) Complex, and localizing to the nucleus to regulate nuclear actin, the nucleolus, and chromatin modifications. The many functions of Fascin must be coordinately regulated to control cell migration. While much remains to be learned about such mechanisms, Fascin is regulated by post-translational modifications, prostaglandin signaling, protein–protein interactions, and transcriptional means. Here, we review the structure of Fascin, the various functions of Fascin and how they contribute to cell migration, the mechanisms regulating Fascin, and how Fascin contributes to diseases, specifically cancer metastasis.
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spelling pubmed-76981962020-11-29 Fascin in Cell Migration: More Than an Actin Bundling Protein Lamb, Maureen C. Tootle, Tina L. Biology (Basel) Review SIMPLE SUMMARY: Cell migration is an essential biological process that regulates both development and diseases, such as cancer metastasis. Therefore, understanding the factors that promote cell migration is crucial. One of the factors known to regulate cell migration is the actin-binding protein, Fascin. Fascin is typically thought to promote cell migration through bundling actin to form migratory structures such as filopodia and invadapodia. However, Fascin has many other functions in the cell that may contribute to cell migration. How these novel functions promote cell migration and are regulated is still not well understood. Here, we review the structure of Fascin, the many functions of Fascin and how they may promote cell migration, how Fascin is regulated, and Fascin’s role in diseases such as cancer metastasis. ABSTRACT: Fascin, an actin-binding protein, regulates many developmental migrations and contributes to cancer metastasis. Specifically, Fascin promotes cell motility, invasion, and adhesion by forming filopodia and invadopodia through its canonical actin bundling function. In addition to bundling actin, Fascin has non-canonical roles in the cell that are thought to promote cell migration. These non-canonical functions include regulating the activity of other actin-binding proteins, binding to and regulating microtubules, mediating mechanotransduction to the nucleus via interaction with the Linker of the Nucleoskeleton and Cytoskeleton (LINC) Complex, and localizing to the nucleus to regulate nuclear actin, the nucleolus, and chromatin modifications. The many functions of Fascin must be coordinately regulated to control cell migration. While much remains to be learned about such mechanisms, Fascin is regulated by post-translational modifications, prostaglandin signaling, protein–protein interactions, and transcriptional means. Here, we review the structure of Fascin, the various functions of Fascin and how they contribute to cell migration, the mechanisms regulating Fascin, and how Fascin contributes to diseases, specifically cancer metastasis. MDPI 2020-11-17 /pmc/articles/PMC7698196/ /pubmed/33212856 http://dx.doi.org/10.3390/biology9110403 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lamb, Maureen C.
Tootle, Tina L.
Fascin in Cell Migration: More Than an Actin Bundling Protein
title Fascin in Cell Migration: More Than an Actin Bundling Protein
title_full Fascin in Cell Migration: More Than an Actin Bundling Protein
title_fullStr Fascin in Cell Migration: More Than an Actin Bundling Protein
title_full_unstemmed Fascin in Cell Migration: More Than an Actin Bundling Protein
title_short Fascin in Cell Migration: More Than an Actin Bundling Protein
title_sort fascin in cell migration: more than an actin bundling protein
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7698196/
https://www.ncbi.nlm.nih.gov/pubmed/33212856
http://dx.doi.org/10.3390/biology9110403
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