Literature DB >> 391780

Cancer cachexia in man: a review.

A J Strain.   

Abstract

There are many factors which are responsible for the high incidence of cachexia in human neoplasia. In this review, those considered to be of major importance are discussed. Nutritional disturbances, such as anorexia and malabsorption, are common and nutritional repletion may be beneficial to certain patients. Raised metabolic rate and energy expenditure are also encountered. Tumour cells may act as a nitrogen trap or energy sink, but the significance of these mechanisms in man is questionable. Ectopic hormone production by tumours is well established and a number of tumour-derived substances have been described which interfere with the intermediary metabolism of the host. The significance of these various substances also remains uncertain. Most experimental studies of cancer cachexia have utilized transplantable animal tumour models which bear a poor resemblance to the clinical condition. Development of more suitable models with human tumour xenografts might allow a quicker and better understanding of the aetiologies of human cancer-induced cachexia.

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Year:  1979        PMID: 391780

Source DB:  PubMed          Journal:  Invest Cell Pathol        ISSN: 0146-7611


  11 in total

Review 1.  Cancer cachexia.

Authors:  M J Tisdale; S A Beck
Journal:  Int J Pancreatol       Date:  1990 Aug-Nov

2.  Elevated venous glutamate levels in (pre)catabolic conditions result at least partly from a decreased glutamate transport activity.

Authors:  V Hack; O Stütz; R Kinscherf; M Schykowski; M Kellerer; E Holm; W Dröge
Journal:  J Mol Med (Berl)       Date:  1996-06       Impact factor: 4.599

3.  Lipopolysaccharide (LPS) increases the in vivo oxidation of branched-chain amino acids in the rat: a cytokine-mediated effect.

Authors:  C García-Martínez; M Llovera; F J López-Soriano; B del Santo; J M Argilés
Journal:  Mol Cell Biochem       Date:  1995-07-05       Impact factor: 3.396

4.  Amino acid uptake in skeletal muscle of rats bearing the Yoshida AH-130 ascites hepatoma.

Authors:  C García-Martínez; F J López-Soriano; J M Argilés
Journal:  Mol Cell Biochem       Date:  1995-07-05       Impact factor: 3.396

5.  The effect of tumor bulk on the metabolic response to cancer.

Authors:  J B Koea; J H Shaw
Journal:  Ann Surg       Date:  1992-03       Impact factor: 12.969

6.  Low plasma glutamine in combination with high glutamate levels indicate risk for loss of body cell mass in healthy individuals: the effect of N-acetyl-cysteine.

Authors:  R Kinscherf; V Hack; T Fischbach; B Friedmann; C Weiss; L Edler; P Bärtsch; W Dröge
Journal:  J Mol Med (Berl)       Date:  1996-07       Impact factor: 4.599

7.  Brown adipose tissue in cancer patients: possible cause of cancer-induced cachexia.

Authors:  F G Shellock; M S Riedinger; M C Fishbein
Journal:  J Cancer Res Clin Oncol       Date:  1986       Impact factor: 4.553

8.  Tumor necrosis factor-alpha mediates changes in tissue protein turnover in a rat cancer cachexia model.

Authors:  P Costelli; N Carbó; L Tessitore; G J Bagby; F J Lopez-Soriano; J M Argilés; F M Baccino
Journal:  J Clin Invest       Date:  1993-12       Impact factor: 14.808

9.  Acute treatment with tumour necrosis factor-alpha induces changes in protein metabolism in rat skeletal muscle.

Authors:  C García-Martínez; F J López-Soriano; J M Argilés
Journal:  Mol Cell Biochem       Date:  1993-08-11       Impact factor: 3.396

10.  Induction of weight loss and metabolic alterations by human recombinant tumour necrosis factor.

Authors:  S M Mahony; M J Tisdale
Journal:  Br J Cancer       Date:  1988-09       Impact factor: 7.640

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