4.7 Article

Identification of Peroxiredoxin-1 as a Novel Biomarker of Abdominal Aortic Aneurysm

Journal

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
Volume 31, Issue 4, Pages 935-U463

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/ATVBAHA.110.214429

Keywords

aneurysms; antioxidants; proteomics

Funding

  1. Fighting aneurysmal disease project [FP-7, HEALTH F2-2008-200647]
  2. Ministerio de Ciencia e Innovacion [SAF2010/21852, SAF2007/63648]
  3. Fundacion Ramon Areces
  4. CAM [S2006/GEN-0247]
  5. Ministerio de Sanidad y Consumo
  6. Instituto de Salud Carlos III
  7. Redes RECAVA [RD06/0014/0035, PI10/00234, EUS2008-03565]
  8. Fundacion Pro CNIC

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Objective-In the search of novel biomarkers of abdominal aortic aneurysm (AAA) progression, proteins released by intraluminal thrombus (ILT) were analyzed by a differential proteomic approach. Methods and Results-Different layers (luminal/abluminal) of the ILT of AAA were incubated, and the proteins released were analyzed by 2-dimensional difference in-gel electrophoresis. Several differentially expressed proteins involved in main AAA pathological mechanisms (proteolysis, oxidative stress, and thrombosis) were identified by mass spectrometry. Among the proteins identified, peroxiredoxin-1 (PRX-1) was more released by the luminal layer compared with the abluminal layer of the ILT, which was further validated by Western blot, ELISA, and immunohistochemistry. We demonstrated increased PRX-1 serum levels in AAA patients compared with healthy subjects and also positive correlation among PRX-1 and AAA diameter, plasmin-antiplasmin, and myeloperoxidase levels. Finally, a prospective study revealed a positive correlation between PRX-1 serum levels and AAA expansion rate. Moreover, the combination of PRX-1 and AAA size had significantly additive value in predicting growth. Conclusion-Several proteins associated with AAA pathogenesis have been identified by a proteomic approach in ILT-conditioned medium. Among them, PRX-1 serum levels are increased in AAA patients and correlate with AAA size and growth rate, suggesting the potential use of PRX-1 as a biomarker for AAA evolution. (Arterioscler Thromb Vasc Biol. 2011;31:935-943.)

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