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The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy
Decline in skeletal muscle cell size (myofiber atrophy) is a key feature of cancer-induced wasting (cachexia). In particular, atrophy of the diaphragm, the major muscle responsible for breathing, is an important determinant of cancer-associated mortality. However, therapeutic options are limited. He...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061726/ https://www.ncbi.nlm.nih.gov/pubmed/35501350 http://dx.doi.org/10.1038/s41467-022-30120-1 |
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author | Graca, Flavia A. Rai, Mamta Hunt, Liam C. Stephan, Anna Wang, Yong-Dong Gordon, Brittney Wang, Ruishan Quarato, Giovanni Xu, Beisi Fan, Yiping Labelle, Myriam Demontis, Fabio |
author_facet | Graca, Flavia A. Rai, Mamta Hunt, Liam C. Stephan, Anna Wang, Yong-Dong Gordon, Brittney Wang, Ruishan Quarato, Giovanni Xu, Beisi Fan, Yiping Labelle, Myriam Demontis, Fabio |
author_sort | Graca, Flavia A. |
collection | PubMed |
description | Decline in skeletal muscle cell size (myofiber atrophy) is a key feature of cancer-induced wasting (cachexia). In particular, atrophy of the diaphragm, the major muscle responsible for breathing, is an important determinant of cancer-associated mortality. However, therapeutic options are limited. Here, we have used Drosophila transgenic screening to identify muscle-secreted factors (myokines) that act as paracrine regulators of myofiber growth. Subsequent testing in mouse myotubes revealed that mouse Fibcd1 is an evolutionary-conserved myokine that preserves myofiber size via ERK signaling. Local administration of recombinant Fibcd1 (rFibcd1) ameliorates cachexia-induced myofiber atrophy in the diaphragm of mice bearing patient-derived melanoma xenografts and LLC carcinomas. Moreover, rFibcd1 impedes cachexia-associated transcriptional changes in the diaphragm. Fibcd1-induced signaling appears to be muscle selective because rFibcd1 increases ERK activity in myotubes but not in several cancer cell lines tested. We propose that rFibcd1 may help reinstate myofiber size in the diaphragm of patients with cancer cachexia. |
format | Online Article Text |
id | pubmed-9061726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90617262022-05-04 The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy Graca, Flavia A. Rai, Mamta Hunt, Liam C. Stephan, Anna Wang, Yong-Dong Gordon, Brittney Wang, Ruishan Quarato, Giovanni Xu, Beisi Fan, Yiping Labelle, Myriam Demontis, Fabio Nat Commun Article Decline in skeletal muscle cell size (myofiber atrophy) is a key feature of cancer-induced wasting (cachexia). In particular, atrophy of the diaphragm, the major muscle responsible for breathing, is an important determinant of cancer-associated mortality. However, therapeutic options are limited. Here, we have used Drosophila transgenic screening to identify muscle-secreted factors (myokines) that act as paracrine regulators of myofiber growth. Subsequent testing in mouse myotubes revealed that mouse Fibcd1 is an evolutionary-conserved myokine that preserves myofiber size via ERK signaling. Local administration of recombinant Fibcd1 (rFibcd1) ameliorates cachexia-induced myofiber atrophy in the diaphragm of mice bearing patient-derived melanoma xenografts and LLC carcinomas. Moreover, rFibcd1 impedes cachexia-associated transcriptional changes in the diaphragm. Fibcd1-induced signaling appears to be muscle selective because rFibcd1 increases ERK activity in myotubes but not in several cancer cell lines tested. We propose that rFibcd1 may help reinstate myofiber size in the diaphragm of patients with cancer cachexia. Nature Publishing Group UK 2022-05-02 /pmc/articles/PMC9061726/ /pubmed/35501350 http://dx.doi.org/10.1038/s41467-022-30120-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Graca, Flavia A. Rai, Mamta Hunt, Liam C. Stephan, Anna Wang, Yong-Dong Gordon, Brittney Wang, Ruishan Quarato, Giovanni Xu, Beisi Fan, Yiping Labelle, Myriam Demontis, Fabio The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy |
title | The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy |
title_full | The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy |
title_fullStr | The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy |
title_full_unstemmed | The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy |
title_short | The myokine Fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy |
title_sort | myokine fibcd1 is an endogenous determinant of myofiber size and mitigates cancer-induced myofiber atrophy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9061726/ https://www.ncbi.nlm.nih.gov/pubmed/35501350 http://dx.doi.org/10.1038/s41467-022-30120-1 |
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