Autophagic-Lysosomal pathway is the main proteolytic system modified in the skeletal muscle of esophageal cancer patients1-3

摘要

Background: In cancer cachexia, muscle depletion is related to morbidity and mortality. Muscle-wasting mechanisms in cancer patients are not fully understood. Objective: We investigated the involvement of the proteolytic systems (proteasome, autophagic-lysosomal, calpain, and caspase) in muscle wasting during cancer cachexia. Design: Esophageal cancer patients n = 14; mean ± SD age: 64.1 ± 6.6 y and weight-stable control patients undergoing reflux surgery (n = 8; age: 57.5 ± 5.8 y) were included. Enzymatic activities were measured in the vastus lateralis and diaphragm. Protein expressions were also measured in the vastus lateralis of control (n =7) and cancer (n = 8) patients.Results: Proteasome, calpain, and caspase 3 activities in the vastuslateralis and diaphragm muscles did not differ between the 2 groups.Cathepsin B and L activities were 90 (±SD) 2.4 ± 0.2 compared with 1.3 ± 0.2 pmol 7-amido-4-methylcoumarin (AMC) · μg protein-1 · min-1; P 0.001 and 115 (5.3 ± 0.4 compared with 2.5 ± 0.3 pmol AMC $ mg protein21 $ min21; P 0.001) greater,respectively, in the vastus lateralis of cancer patients than in that of control subjects. We observed (in conjunction with increased lysosomal protease activities) higher microtubule-associated protein 1 light chain 3B-2/1 ratios (0.14 ± 0.08 compared with 0.04 ± 0.04) and cathepsin B and L expressions in the vastus lateralis of cancer patients than in that of control subjects (P 0.05). Protein expression of p62 in the vastus lateralis did not differ between the 2 groups. Conclusions: The autophagic-lysosomal pathway in the skeletal muscle of cancer patients was modified, whereas other proteolytic systems were unchanged. These findings suggest involvement of the autophagic-lysosomal proteolytic system during cancer cachexia development in humans.