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Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening.
Otero-Estévez, Olalla; De Chiara, Loretta; Rodríguez-Girondo, Mar; Rodríguez-Berrocal, Francisco Javier; Cubiella, Joaquín; Castro, Inés; Hernández, Vicent; Martínez-Zorzano, Vicenta Soledad.
Afiliação
  • Otero-Estévez O; Department of Biochemistry, Genetics and Immunology, Universidade de Vigo. Vigo, Spain.
  • De Chiara L; Department of Biochemistry, Genetics and Immunology, Universidade de Vigo. Vigo, Spain.
  • Rodríguez-Girondo M; SiDOR Research Group &Centro de Investigaciones Biomédicas (CINBIO), Universidade de Vigo. Vigo, Spain.
  • Rodríguez-Berrocal FJ; Department of Biochemistry, Genetics and Immunology, Universidade de Vigo. Vigo, Spain.
  • Cubiella J; Department of Gastroenterology, Complexo Hospitalario Universitario de Ourense. Ourense, Spain.
  • Castro I; Department of Gastroenterology, Complexo Hospitalario Universitario de Ourense. Ourense, Spain.
  • Hernández V; Department of Gastroenterology, Complexo Hospitalario Universitario de Vigo. Vigo, Spain.
  • Martínez-Zorzano VS; Department of Biochemistry, Genetics and Immunology, Universidade de Vigo. Vigo, Spain.
Sci Rep ; 5: 13030, 2015 Aug 12.
Article em En | MEDLINE | ID: mdl-26264519
Matrix metalloproteinase-9 (MMP-9) is related to tumour development and progression in colorectal cancer (CRC) and its utility as biomarker has been suggested. The aim of our study was to measure serum MMP-9 in asymptomatic first-degree relatives of CRC patients, and to analyse its diagnostic accuracy for the detection of advanced neoplasia (AN: advanced adenomas and CRC). Additionally, we compared its diagnostic capability with the most used non-invasive faecal immunochemical test (FIT). Serum MMP-9 was quantified by ELISA in 516 asymptomatic individuals that underwent a colonoscopy and a FIT. MMP-9 levels were significantly related to age and gender and therefore the concentration was corrected by these confounders. Corrected MMP-9 (cMMP-9) levels were higher in individuals with advanced adenomas (AA; p-value = 0.029) and AN (p-value = 0.056) compared to individuals with no neoplasia. Moreover, elevated cMMP-9 concentration was associated with more severe characteristics of adenomas (number of lesions, size and histology). Nevertheless, the diagnostic accuracy of cMMP-9 was considerably lower than that of FIT for identifying AA (22.64% vs. 47.17% sensitivity, 90% specificity) or AN (19.30% vs. 52.63% sensitivity, 90% specificity). According to our results, serum MMP-9 cannot be considered of utility for the diagnosis of AN in CRC family-risk population screening.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Biomarcadores Tumorais / Metaloproteinase 9 da Matriz Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Biomarcadores Tumorais / Metaloproteinase 9 da Matriz Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Sci Rep Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Espanha