Prognostic significance of TIMP-1 in non-small cell lung cancer
Jazyk angličtina Země Řecko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
22110238
PII: 31/11/4031
Knihovny.cz E-zdroje
- MeSH
- adenokarcinom diagnóza genetika mortalita MeSH
- dospělí MeSH
- ELISA MeSH
- lidé středního věku MeSH
- lidé MeSH
- messenger RNA genetika MeSH
- míra přežití MeSH
- nádorové biomarkery krev genetika MeSH
- nádory plic diagnóza genetika mortalita MeSH
- nemalobuněčný karcinom plic diagnóza genetika mortalita MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- prognóza MeSH
- senioři MeSH
- spinocelulární karcinom diagnóza genetika mortalita MeSH
- staging nádorů MeSH
- tkáňový inhibitor metaloproteinasy 1 krev genetika MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- messenger RNA MeSH
- nádorové biomarkery MeSH
- TIMP1 protein, human MeSH Prohlížeč
- tkáňový inhibitor metaloproteinasy 1 MeSH
UNLABELLED: Tissue inhibitor of metalloproteinases 1 (TIMP1) regulates not only extracellular matrix catabolism but the major effect in tumor tissue is promotion of cell growth and anti-apoptotic activity. The aim of our study was to evaluate plasma TIMP1 levels and tissue TIMP1 mRNA expression as prognostic markers in NSCLC patients. PATIENTS AND METHODS: We studied a group of 108 patients with NSCLC who had undergone lung surgery. Estimation of TIMP1 mRNA was performed by quantitative polymerase chain reaction (qPCR) and estimation of plasma TIMP1 protein using enzyme-linked immunosorbent assay (ELISA). RESULTS: There was shorter disease-free interval (DFI) for NSCLC patients at stage II, with a higher expression of TIMP1 mRNA in tumor tissue (p=0.0246). We recorded a relationship between tumor tissue TIMP1 mRNA expression and DFI in squamous cell carcinoma (SCC) (p=0.0117). Shorter overall survival was found in patients at stages IIIa+IIIb+IV, with a higher expression of TIMP1 mRNA (p=0.0389). We found differences in plasma TIMP1 levels between patients with SCC and those with adenocarcinoma (p=0.0491). CONCLUSION: A higher tissue level of TIMP1 mRNA is related to an adverse prognosis of patients. However, our results did not show any relation of TIMP1 protein in blood plasma to prognosis.