Dipeptidyl-Peptidase IV Activity Is Correlated with Colorectal Cancer Prognosis


Autoria(s): Larrinaga Embeita, Gorka; Pérez Urzelai, Itxaro; Sanz Echevarría, María Begoña; Beitia San Vicente, Maider; Errarte Yarza, Peio; Fernández Atucha, Ainhoa; Blanco Criado, Lorena; Etxezarraga Zuloaga, María Carmen; Gil Goicouría, Francisco Javier; López Fernández de Villaverde, José Ignacio
Data(s)

02/05/2016

02/05/2016

19/03/2015

Resumo

Background Dipeptidyl-peptidase IV (EC 3.4.14.5) (DPPIV) is a serine peptidase involved in cell differentiation, adhesion, immune modulation and apoptosis, functions that control neoplastic transformation. Previous studies have demonstrated altered expression and activity of tissue and circulating DPPIV in several cancers and proposed its potential usefulness for early diagnosis in colorectal cancer (CRC). Methods and principal findings The activity and mRNA and protein expression of DPPIV was prospectively analyzed in adenocarcinomas, adenomas, uninvolved colorectal mucosa and plasma from 116 CRC patients by fluorimetric, quantitative RT-PCR and immunohistochemical methods. Results were correlated with the most important classic pathological data related to aggressiveness and with 5-year survival rates. Results showed that: 1) mRNA levels and activity of DPPIV increased in colorectal neoplasms (Kruskal-Wallis test, p<0.01); 2) Both adenomas and CRCs displayed positive cytoplasmic immunostaining with luminal membrane reinforcement; 3) Plasmatic DPPIV activity was lower in CRC patients than in healthy subjects (Mann-U test, p<0.01); 4) Plasmatic DPPIV activity was associated with worse overall and disease-free survivals (log-rank p<0.01, Cox analysis p<0.01). Conclusion/significance 1) Up-regulation of DPPIV in colorectal tumors suggests a role for this enzyme in the neoplastic transformation of colorectal tissues. This finding opens the possibility for new therapeutic targets in these patients. 2) Plasmatic DPPIV is an independent prognostic factor in survival of CRC patients. The determination of DPPIV activity levels in the plasma may be a safe, minimally invasive and inexpensive way to define the aggressiveness of CRC in daily practice.

Identificador

Plos One 10(3) 2015 : (2015) // Article ID e0119436

1932-6203

http://hdl.handle.net/10810/18143

10.1371/journal.pone.0119436

Idioma(s)

eng

Publicador

Public Library Science

Relação

http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0119436#abstract0

Direitos

© 2015 Larrinaga et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited

info:eu-repo/semantics/openAccess

Palavras-Chave #fibroblast activation protein #carcinoma-associated fibroblasts #colon-cancer #aminopeptidase N/CD13 #serum CD26 #expression #markers #impact
Tipo

info:eu-repo/semantics/article