Literature DB >> 10232651

The role of cytokines in cancer cachexia.

J M Argilés1, F J López-Soriano.   

Abstract

A large number of observations point towards cytokines, polypeptides released mainly by immune cells, as the molecules responsible for the metabolic derangements associated with cancer-bearing states. Indeed, these alterations lead to a pathological state known as cancer cachexia which is, unfortunately, one of the worst effects of malignancy, accounting for nearly a third of cancer deaths. It is characterized by weight loss together with anorexia, weakness, anemia, and asthenia. The complications associated with the appearance of the cachectic syndrome affect both the physiological and biochemical balance of the patient and have effects on the efficiency of the anticancer treatment, resulting in a considerably decreased survival time. At the metabolic level, cachexia is associated with loss of skeletal muscle protein together with a depletion of body lipid stores. The cachectic patient, in addition to having practically no adipose tissue, is basically subject to an important muscle wastage manifested as an excessive nitrogen loss. The metabolic changes are partially mediated by alterations in circulating hormone concentrations (insulin, glucagon, and glucocorticoids in particular) or in their effectiveness. The present study reviews the involvement of different cytokines in the metabolic and physiological alterations associated with tumor burden and cachexia. Among these cytokines, some can be considered as procachectic (such as tumor necrosis factor-alpha), while others having opposite effects can be named as anticachectic cytokines. It is the balance between these two cytokine types that finally seems to have a key role in cancer cachexia.

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Year:  1999        PMID: 10232651     DOI: 10.1002/(sici)1098-1128(199905)19:3<223::aid-med3>3.0.co;2-n

Source DB:  PubMed          Journal:  Med Res Rev        ISSN: 0198-6325            Impact factor:   12.944


  40 in total

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Review 2.  Proteolysis in illness-associated skeletal muscle atrophy: from pathways to networks.

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3.  Quercetin supplementation attenuates the progression of cancer cachexia in ApcMin/+ mice.

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Journal:  J Nutr       Date:  2014-04-23       Impact factor: 4.798

4.  Dangerous nutrition? Calcium, vitamin D, and shark cartilage nutritional supplements and cancer-related hypercalcemia.

Authors:  Ruth Lagman; Declan Walsh
Journal:  Support Care Cancer       Date:  2003-01-15       Impact factor: 3.603

Review 5.  The role of interleukin-6 in the evolution of ovarian cancer: clinical and prognostic implications--a review.

Authors:  Antonio Macciò; Clelia Madeddu
Journal:  J Mol Med (Berl)       Date:  2013-09-21       Impact factor: 4.599

6.  Glutathione depletion impairs myogenic differentiation of murine skeletal muscle C2C12 cells through sustained NF-kappaB activation.

Authors:  Esther Ardite; Joan Albert Barbera; Josep Roca; Jose C Fernández-Checa
Journal:  Am J Pathol       Date:  2004-09       Impact factor: 4.307

7.  MG132-mediated inhibition of the ubiquitin-proteasome pathway ameliorates cancer cachexia.

Authors:  Liuping Zhang; Hua Tang; Yao Kou; Rui Li; Yueyong Zheng; Qiang Wang; Xiaoyu Zhou; Liangbin Jin
Journal:  J Cancer Res Clin Oncol       Date:  2013-03-28       Impact factor: 4.553

8.  Reversal of muscle atrophy by Zhimu and Huangbai herb pair via activation of IGF-1/Akt and autophagy signal in cancer cachexia.

Authors:  Pengwei Zhuang; Jinbao Zhang; Yan Wang; Mixia Zhang; Lili Song; Zhiqiang Lu; Lu Zhang; Fengqi Zhang; Jing Wang; Yanjun Zhang; Hongjun Wei; Hongyan Li
Journal:  Support Care Cancer       Date:  2015-08-18       Impact factor: 3.603

9.  The effect of cyproheptadine hydrochloride (periactin) and megestrol acetate (megace) on weight in children with cancer/treatment-related cachexia.

Authors:  Marisa Couluris; Jennifer L R Mayer; David R Freyer; Eric Sandler; Ping Xu; Jeffrey P Krischer
Journal:  J Pediatr Hematol Oncol       Date:  2008-11       Impact factor: 1.289

10.  Altered endochondral ossification in collagen X mouse models leads to impaired immune responses.

Authors:  E Sweeney; M Campbell; K Watkins; C A Hunter; O Jacenko
Journal:  Dev Dyn       Date:  2008-10       Impact factor: 3.780

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