| Literature DB >> 28979816 |
Roberto Mota1,2, Jessica E Rodríguez3,4, Andrea Bonetto5,6,7,8, Thomas M O'Connell6,7,8,9, Scott A Asher9,10, Traci L Parry1,3, Pamela Lockyer1,3, Christopher R McCudden3,11, Marion E Couch6,7,9, Monte S Willis1,3,12.
Abstract
Cancer cachexia is a severe wasting syndrome characterized by the progressive loss of lean body mass and systemic inflammation. Up to 80% of cancer patients experience cachexia, with 20-30% of cancer-related deaths directly linked to cachexia. Despite efforts to identify early cachexia and cancer relapse, clinically useful markers are lacking. Recently, we identified the role of muscle-specific ubiquitin ligases Atrogin-1 (MAFbx, FBXO32) and Muscle Ring Finger-1 in the pathogenesis of cardiac atrophy and hypertrophy. We hypothesized that during cachexia, the Atrogin-1 and MuRF1 ubiquitin ligases are released from muscle and migrate to the circulation where they could be detected and serve as a cachexia biomarker. To test this, we induced cachexia in mice using the C26 adenocarcinoma cells or vehicle (control). Body weight, tumor volume, and food consumption were measured from inoculation until ~day 14 to document cachexia. Western blot analysis of serum identified the presence of Atrogin-1 and MuRF1 with unique post-translational modifications consistent with mono- and poly- ubiquitination of Atrogin-1 and MuRF1 found only in cachectic serum. These findings suggest that both increased Atrogin-1 and the presence of unique post-translational modifications may serve as a surrogate marker specific for cachexia.Entities:
Keywords: Atrogin-1; Cancer cachexia; FBXO32; TRIM63; biomarkers; muscle ring Finger-1
Year: 2017 PMID: 28979816 PMCID: PMC5622228
Source DB: PubMed Journal: Am J Cancer Res ISSN: 2156-6976 Impact factor: 6.166