1. Academic Validation
  2. Circulating carnosine dipeptidase 1 associates with weight loss and poor prognosis in gastrointestinal cancer

Circulating carnosine dipeptidase 1 associates with weight loss and poor prognosis in gastrointestinal cancer

  • PLoS One. 2015 Apr 21;10(4):e0123566. doi: 10.1371/journal.pone.0123566.
Peter Arner 1 Frauke Henjes 2 Jochen M Schwenk 2 Spyros Darmanis 2 Ingrid Dahlman 1 Britt-Marie Iresjö 3 Peter Naredi 3 Thorhallur Agustsson 4 Kent Lundholm 3 Peter Nilsson 2 Mikael Rydén 1
Affiliations

Affiliations

  • 1 Department of Medicine (H7), Karolinska Institutet, Karolinska University Hospital, Huddinge, 141 86, Stockholm, Sweden.
  • 2 Affinity Proteomics, Science for Life Laboratory, School of Biotechnology, Royal Institute of Technology, Box 1031, 171 21, Solna, Sweden.
  • 3 Department of Surgery, Sahlgrenska Academy, University of Gothenburg, 413 45, Gothenburg, Sweden.
  • 4 Division of Surgery, Department for Clinical Science, Intervention and Technology (CLINTEC), Södersjukhuset, 118 83, Stockholm, Sweden.
Abstract

Background: Cancer cachexia (CC) is linked to poor prognosis. Although the mechanisms promoting this condition are not known, several circulating proteins have been proposed to contribute. We analyzed the plasma proteome in Cancer subjects in order to identify factors associated with cachexia.

Design/subjects: Plasma was obtained from a screening cohort of 59 patients, newly diagnosed with suspected gastrointestinal Cancer, with (n = 32) or without (n = 27) cachexia. Samples were subjected to proteomic profiling using 760 Antibodies (targeting 698 individual proteins) from the Human Protein Atlas project. The main findings were validated in a cohort of 93 patients with verified and advanced pancreas Cancer.

Results: Only six proteins displayed differential plasma levels in the screening cohort. Among these, Carnosine Dipeptidase 1 (CNDP1) was confirmed by sandwich immunoassay to be lower in CC (p = 0.008). In both cohorts, low CNDP1 levels were associated with markers of poor prognosis including weight loss, malnutrition, lipid breakdown, low circulating albumin/IGF1 levels and poor quality of life. Eleven of the subjects in the discovery cohort were finally diagnosed with non-malignant disease but omitting these subjects from the analyses did not have any major influence on the results.

Conclusions: In gastrointestinal Cancer, reduced plasma levels of CNDP1 associate with signs of catabolism and poor outcome. These results, together with recently published data demonstrating lower circulating CNDP1 in subjects with glioblastoma and metastatic prostate Cancer, suggest that CNDP1 may constitute a marker of aggressive Cancer and CC.

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