<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T05:17:59Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/8263" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/8263</identifier><datestamp>2025-12-04T21:13:15Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478781</setSpec><setSpec>col_2072_478917</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Tumor necrosis factor-alpha mediates changes in tissue protein turnover in a rat cancer cachexia model.</dc:title>
   <dc:creator>Costelli, Paola</dc:creator>
   <dc:creator>Carbó Carbó, Neus</dc:creator>
   <dc:creator>Tessitore, Luciana</dc:creator>
   <dc:creator>Bagby, Gregory J.</dc:creator>
   <dc:creator>López-Soriano, Francisco J.</dc:creator>
   <dc:creator>Argilés Huguet, Josep Ma.</dc:creator>
   <dc:creator>Baccino, Francesco M.</dc:creator>
   <dc:subject>Tumors</dc:subject>
   <dc:subject>Necrosi</dc:subject>
   <dc:subject>Músculs</dc:subject>
   <dc:subject>Tumor necrosis factor</dc:subject>
   <dc:subject>Skeletal muscle</dc:subject>
   <dc:subject>Protein turnover</dc:subject>
   <dc:description>Rats bearing the Yoshida AH-130 ascites hepatoma showed enhanced fractional rates of protein degradation in gastrocnemius muscle, heart, and liver, while fractional synthesis rates were similar to those in non-tumor bearing rats. This hypercatabolic pattern was associated with marked perturbations of the hormonal homeostasis and presence of tumor necrosis factor in the circulation. The daily administration of a goat anti-murine TNF IgG to tumor-bearing rats decreased protein degradation rates in skeletal muscle, heart, and liver as compared with tumor-bearing rats receiving a nonimmune goat IgG. The anti-TNF treatment was also effective in attenuating early perturbations in insulin and corticosterone homeostasis. Although these results suggest that tumor necrosis factor plays a significant role in mediating the changes in protein turnover and hormone levels elicited by tumor growth, the inability of such treatment to prevent a reduction in body weight implies that other mediators or tumor-related events were also involved.</dc:description>
   <dc:date>2009-05-14T10:14:17Z</dc:date>
   <dc:date>2009-05-14T10:14:17Z</dc:date>
   <dc:date>1993</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>0021-9738</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/8263</dc:identifier>
   <dc:identifier>79740</dc:identifier>
   <dc:identifier>8254032</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a http://dx.doi.org/doi:10.1172/JCI116897</dc:relation>
   <dc:relation>Journal of Clinical Investigation, 1993, vol. 92, núm. 6, p. 2783-2789.</dc:relation>
   <dc:rights>(c) The American Society for Clinical Investigation, 1993</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>7 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>American Society for Clinical Investigation</dc:publisher>
   <dc:source>Articles publicats en revistes (Bioquímica i Biomedicina Molecular)</dc:source>
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