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Caldesmon: Biochemical and Clinical Implications in Cancer
Caldesmon, an actin-binding protein, can inhibit myosin binding to actin and regulate smooth muscle contraction and relaxation. However, caldesmon has recently attracted attention due to its importance in cancer. The upregulation of caldesmon in several solid cancer tissues has been reported. Caldes...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930484/ https://www.ncbi.nlm.nih.gov/pubmed/33681215 http://dx.doi.org/10.3389/fcell.2021.634759 |
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author | Yao, Yi-Bo Xiao, Chang-Fang Lu, Jin-Gen Wang, Chen |
author_facet | Yao, Yi-Bo Xiao, Chang-Fang Lu, Jin-Gen Wang, Chen |
author_sort | Yao, Yi-Bo |
collection | PubMed |
description | Caldesmon, an actin-binding protein, can inhibit myosin binding to actin and regulate smooth muscle contraction and relaxation. However, caldesmon has recently attracted attention due to its importance in cancer. The upregulation of caldesmon in several solid cancer tissues has been reported. Caldesmon, as well as its two isoforms, is considered as a biomarker for cancer and a potent suppressor of cancer cell invasion by regulating podosome/invadopodium formation. Therefore, caldesmon may be a promising therapeutic target for diseases such as cancer. Here, we review new studies on the gene transcription, isoform structure, expression, and phosphorylation regulation of caldesmon and discuss its clinical implications in cancer. |
format | Online Article Text |
id | pubmed-7930484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79304842021-03-05 Caldesmon: Biochemical and Clinical Implications in Cancer Yao, Yi-Bo Xiao, Chang-Fang Lu, Jin-Gen Wang, Chen Front Cell Dev Biol Cell and Developmental Biology Caldesmon, an actin-binding protein, can inhibit myosin binding to actin and regulate smooth muscle contraction and relaxation. However, caldesmon has recently attracted attention due to its importance in cancer. The upregulation of caldesmon in several solid cancer tissues has been reported. Caldesmon, as well as its two isoforms, is considered as a biomarker for cancer and a potent suppressor of cancer cell invasion by regulating podosome/invadopodium formation. Therefore, caldesmon may be a promising therapeutic target for diseases such as cancer. Here, we review new studies on the gene transcription, isoform structure, expression, and phosphorylation regulation of caldesmon and discuss its clinical implications in cancer. Frontiers Media S.A. 2021-02-18 /pmc/articles/PMC7930484/ /pubmed/33681215 http://dx.doi.org/10.3389/fcell.2021.634759 Text en Copyright © 2021 Yao, Xiao, Lu and Wang. http://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 | Cell and Developmental Biology Yao, Yi-Bo Xiao, Chang-Fang Lu, Jin-Gen Wang, Chen Caldesmon: Biochemical and Clinical Implications in Cancer |
title | Caldesmon: Biochemical and Clinical Implications in Cancer |
title_full | Caldesmon: Biochemical and Clinical Implications in Cancer |
title_fullStr | Caldesmon: Biochemical and Clinical Implications in Cancer |
title_full_unstemmed | Caldesmon: Biochemical and Clinical Implications in Cancer |
title_short | Caldesmon: Biochemical and Clinical Implications in Cancer |
title_sort | caldesmon: biochemical and clinical implications in cancer |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7930484/ https://www.ncbi.nlm.nih.gov/pubmed/33681215 http://dx.doi.org/10.3389/fcell.2021.634759 |
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