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Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes
BACKGROUND: Patients with advanced cancer suffer from cachexia, which is characterised by a marked weight loss, and is invariably associated with the presence of tumoral and humoral factors which are mainly responsible for the depletion of fat stores and muscular tissue. METHODS: In this work, we us...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266935/ https://www.ncbi.nlm.nih.gov/pubmed/18226207 http://dx.doi.org/10.1186/1471-2407-8-24 |
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author | Yano, Claudia L Ventrucci, Gislaine Field, William N Tisdale, Michael J Gomes-Marcondes, Maria Cristina C |
author_facet | Yano, Claudia L Ventrucci, Gislaine Field, William N Tisdale, Michael J Gomes-Marcondes, Maria Cristina C |
author_sort | Yano, Claudia L |
collection | PubMed |
description | BACKGROUND: Patients with advanced cancer suffer from cachexia, which is characterised by a marked weight loss, and is invariably associated with the presence of tumoral and humoral factors which are mainly responsible for the depletion of fat stores and muscular tissue. METHODS: In this work, we used cytotoxicity and enzymatic assays and morphological analysis to examine the effects of a proteolysis-inducing factor (PIF)-like molecule purified from ascitic fluid of Walker tumour-bearing rats (WF), which has been suggested to be responsible for muscle atrophy, on cultured C(2)C(12 )muscle cells. RESULTS: WF decreased the viability of C(2)C(12 )myotubes, especially at concentrations of 20–25 μg.mL(-1). There was an increase in the content of the pro-oxidant malondialdehyde, and a decrease in antioxidant enzyme activity. Myotubes protein synthesis decreased and protein degradation increased together with an enhanced in the chymotrypsin-like enzyme activity, a measure of functional proteasome activity, after treatment with WF. Morphological alterations such as cell retraction and the presence of numerous cells in suspension were observed, particularly at high WF concentrations. CONCLUSION: These results indicate that WF has similar effects to those of proteolysis-inducing factor, but is less potent than the latter. Further studies are required to determine the precise role of WF in this experimental model. |
format | Text |
id | pubmed-2266935 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22669352008-03-12 Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes Yano, Claudia L Ventrucci, Gislaine Field, William N Tisdale, Michael J Gomes-Marcondes, Maria Cristina C BMC Cancer Research Article BACKGROUND: Patients with advanced cancer suffer from cachexia, which is characterised by a marked weight loss, and is invariably associated with the presence of tumoral and humoral factors which are mainly responsible for the depletion of fat stores and muscular tissue. METHODS: In this work, we used cytotoxicity and enzymatic assays and morphological analysis to examine the effects of a proteolysis-inducing factor (PIF)-like molecule purified from ascitic fluid of Walker tumour-bearing rats (WF), which has been suggested to be responsible for muscle atrophy, on cultured C(2)C(12 )muscle cells. RESULTS: WF decreased the viability of C(2)C(12 )myotubes, especially at concentrations of 20–25 μg.mL(-1). There was an increase in the content of the pro-oxidant malondialdehyde, and a decrease in antioxidant enzyme activity. Myotubes protein synthesis decreased and protein degradation increased together with an enhanced in the chymotrypsin-like enzyme activity, a measure of functional proteasome activity, after treatment with WF. Morphological alterations such as cell retraction and the presence of numerous cells in suspension were observed, particularly at high WF concentrations. CONCLUSION: These results indicate that WF has similar effects to those of proteolysis-inducing factor, but is less potent than the latter. Further studies are required to determine the precise role of WF in this experimental model. BioMed Central 2008-01-28 /pmc/articles/PMC2266935/ /pubmed/18226207 http://dx.doi.org/10.1186/1471-2407-8-24 Text en Copyright © 2008 Yano et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yano, Claudia L Ventrucci, Gislaine Field, William N Tisdale, Michael J Gomes-Marcondes, Maria Cristina C Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes |
title | Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes |
title_full | Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes |
title_fullStr | Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes |
title_full_unstemmed | Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes |
title_short | Metabolic and morphological alterations induced by proteolysis-inducing factor from Walker tumour-bearing rats in C(2)C(12 )myotubes |
title_sort | metabolic and morphological alterations induced by proteolysis-inducing factor from walker tumour-bearing rats in c(2)c(12 )myotubes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266935/ https://www.ncbi.nlm.nih.gov/pubmed/18226207 http://dx.doi.org/10.1186/1471-2407-8-24 |
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