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Pismo Towarzystwa Internistów Polskich, założone przez prof. Władysława Antoniego Gluzińskiego
Pismo indeksowane w:
MEDLINE/Index Medicus,
EMBASE/Excerpta Medica Database,
Index Copernicus (IC), KBN/MNiSW,
Polish Medical Library (GBL), EBSCO,
ISI Science Citation Index Expanded,
Scopus,
Directory of Open Access Journals (DOAJ)
Wartość Index Copernicus (IC) za 2010: 9 pkt,
punktacja MNiSW: 9 pkt.
Czasopismo dofinansowywane przez MNiSW w ramach działalności wspomagającej badania.
Polskie Archiwum Medycyny Wewnętrznej jest czasopismem typu "open-access" i gwarantuje darmowy dostęp do pełnej treści artykułów.
Marta Łukaszewicz‑Zając, Barbara Mroczko, Mirosław Kozłowski, Jacek Nikliński, Jerzy Laudański, Maciej Szmitkowski
Abstrakt
Introduction Matrix metalloproteinase 9 (MMP‑9) is a proteolytic enzyme which is associated with tumor progression including invasion, migration, angiogenesis, and metastasis due to its ability to degrade type IV collagen.
Objectives The aim of the study was to assess clinical significance of MMP‑9 measurement in the diagnostic evaluation of patients with esophageal squamous cell carcinoma (ESCC).
Patients and methods The study included 63 patients with ESCC and 30 healthy subjects. We assayed serum MMP‑9 levels and squamous cell carcinoma antigen (SCC‑Ag), a tumor marker. We defined diagnostic criteria for both markers.
Results In ESCC patients serum levels of MMP‑9 and SCC‑Ag were found to be statistically higher compared with healthy subjects. Serum concentrations of MMP‑9 and SCC‑Ag tended to increase in patients with advanced cancer. The percentage of elevated MMP‑9 concentrations (75%) was higher than that of SCC‑Ag (68%) and increased for the combined use of both markers (97%).
Conclusions The results suggest the potential usefulness of MMP‑9 in establishing the diagnosis of ESCC, especially when analyzed in combination with SCC‑Ag.
Słowa kluczowe
esophageal squamous cell carcinoma, matrix metalloproteinase 9
Pol Arch Med Wewn, 2009; 119 (9): 558-563
PMID: 19776700
Pobierz artykuł (PDF): EN abstrakt PL