Literature DB >> 9801160

Skeletal muscle UCP2 and UCP3 gene expression in a rat cancer cachexia model.

D Sanchís1, S Busquets, B Alvarez, D Ricquier, F J López-Soriano, J M Argilés.   

Abstract

Rats bearing the Yoshida AH-130 ascites hepatoma showed an increased expression of both uncoupling protein-2 (UCP2) (194%) and UCP3 (189%) mRNA levels in skeletal muscle 7 days after tumour inoculation. Interestingly, an even greater increase was observed in mRNA for both UCP2 (278%) and UCP3 (797%) in the pair-fed animals, suggesting that the increase in gene expression was the result of the anorexia associated with tumour burden. The results constitute the first report of UCP2 and UCP3 gene expression during cancer cachexia and agree to their possible role in the increase of energy expenditure associated with tumour growth.

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Year:  1998        PMID: 9801160     DOI: 10.1016/s0014-5793(98)01178-8

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  20 in total

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3.  Prevention of unloading-induced atrophy by vitamin E supplementation: links between oxidative stress and soleus muscle proteolysis?

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4.  Formoterol treatment downregulates the myostatin system in skeletal muscle of cachectic tumour-bearing rats.

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Review 5.  Overexpression of uncoupling protein-2 in cancer: metabolic and heat changes, inhibition and effects on drug resistance.

Authors:  Michael A Pitt
Journal:  Inflammopharmacology       Date:  2015-11-05       Impact factor: 4.473

Review 6.  Exosomal microRNAs in cancer-related sarcopenia: Tumor-derived exosomal microRNAs in muscle atrophy.

Authors:  Chenyuan Li; Qi Wu; Zhiyu Li; Zhong Wang; Yi Tu; Chuang Chen; Si Sun; Shengrong Sun
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7.  Myostatin blockage using actRIIB antagonism in mice bearing the Lewis lung carcinoma results in the improvement of muscle wasting and physical performance.

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8.  Cancer cachexia is associated with a decrease in skeletal muscle mitochondrial oxidative capacities without alteration of ATP production efficiency.

Authors:  Cloé M Julienne; Jean-François Dumas; Caroline Goupille; Michelle Pinault; Cécile Berri; Anne Collin; Sophie Tesseraud; Charles Couet; Stephane Servais
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9.  Nuclear magnetic resonance in conjunction with functional genomics suggests mitochondrial dysfunction in a murine model of cancer cachexia.

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10.  Sirtuin 1 in skeletal muscle of cachectic tumour-bearing rats: a role in impaired regeneration?

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Journal:  J Cachexia Sarcopenia Muscle       Date:  2011-02-24       Impact factor: 12.910

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