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Cancer cachexia: lessons from Drosophila

Cachexia, a wasting syndrome that is often associated with cancer, is one of the primary causes of death in cancer patients. Cancer cachexia occurs largely due to systemic metabolic alterations stimulated by tumors. Despite the prevalence of cachexia, our understanding of how tumors interact with ho...

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Autores principales: Liu, Ying, Saavedra, Pedro, Perrimon, Norbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961677/
https://www.ncbi.nlm.nih.gov/pubmed/35319749
http://dx.doi.org/10.1242/dmm.049298
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author Liu, Ying
Saavedra, Pedro
Perrimon, Norbert
author_facet Liu, Ying
Saavedra, Pedro
Perrimon, Norbert
author_sort Liu, Ying
collection PubMed
description Cachexia, a wasting syndrome that is often associated with cancer, is one of the primary causes of death in cancer patients. Cancer cachexia occurs largely due to systemic metabolic alterations stimulated by tumors. Despite the prevalence of cachexia, our understanding of how tumors interact with host tissues and how they affect metabolism is limited. Among the challenges of studying tumor–host tissue crosstalk are the complexity of cancer itself and our insufficient knowledge of the factors that tumors release into the blood. Drosophila is emerging as a powerful model in which to identify tumor-derived factors that influence systemic metabolism and tissue wasting. Strikingly, studies that are characterizing factors derived from different fly tumor cachexia models are identifying both common and distinct cachectic molecules, suggesting that cachexia is more than one disease and that fly models can help identify these differences. Here, we review what has been learned from studies of tumor-induced organ wasting in Drosophila and discuss the open questions.
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spelling pubmed-89616772022-03-29 Cancer cachexia: lessons from Drosophila Liu, Ying Saavedra, Pedro Perrimon, Norbert Dis Model Mech Review Cachexia, a wasting syndrome that is often associated with cancer, is one of the primary causes of death in cancer patients. Cancer cachexia occurs largely due to systemic metabolic alterations stimulated by tumors. Despite the prevalence of cachexia, our understanding of how tumors interact with host tissues and how they affect metabolism is limited. Among the challenges of studying tumor–host tissue crosstalk are the complexity of cancer itself and our insufficient knowledge of the factors that tumors release into the blood. Drosophila is emerging as a powerful model in which to identify tumor-derived factors that influence systemic metabolism and tissue wasting. Strikingly, studies that are characterizing factors derived from different fly tumor cachexia models are identifying both common and distinct cachectic molecules, suggesting that cachexia is more than one disease and that fly models can help identify these differences. Here, we review what has been learned from studies of tumor-induced organ wasting in Drosophila and discuss the open questions. The Company of Biologists Ltd 2022-03-23 /pmc/articles/PMC8961677/ /pubmed/35319749 http://dx.doi.org/10.1242/dmm.049298 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Review
Liu, Ying
Saavedra, Pedro
Perrimon, Norbert
Cancer cachexia: lessons from Drosophila
title Cancer cachexia: lessons from Drosophila
title_full Cancer cachexia: lessons from Drosophila
title_fullStr Cancer cachexia: lessons from Drosophila
title_full_unstemmed Cancer cachexia: lessons from Drosophila
title_short Cancer cachexia: lessons from Drosophila
title_sort cancer cachexia: lessons from drosophila
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8961677/
https://www.ncbi.nlm.nih.gov/pubmed/35319749
http://dx.doi.org/10.1242/dmm.049298
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