Povzetek
Metalloproteinases (MMPs) have an important role in tissue remodeling and have been shown to have an effect on tumor progression, invasion, metastasis formation, and apoptosis in several tumors, including mesothelioma. Mesothelioma is a rare tumor arising from pleura and peritoneum and is frequently associated with asbestos exposure. We have performed a systematic search of PubMed.gov and ClinicalTrials.gov databases to retrieve and review three groups of studies: studies of MMPs expression in tumor tissue or body fluids in patients with mesothelioma, studies of MMPs genetic variability, and studies of MMPs as potential novel drug targets in mesothelioma. Several studies of MMPs in mesothelioma tissues reported a link between higher expression levels of commonly studied MMPs and clinical parameters, such as overall survival. Fewer studies have investigated genetic variability of MMP genes. Nevertheless, these studies suggested that certain genetic variants in MMP genes can have either protective or tumor-promoting effects on mesothelioma patients. MMPs have been also reported as novel drug targets, but so far no clinical trials of MMP inhibitors are registered in mesothelioma. In conclusion, MMPs play an important role in mesothelioma, but further studies are needed to elucidate the potentials of MMPs as biomarkers and drug targets in mesothelioma.
Ključne besede
mezoteliom;metaloproteinaza;genetska variabilnost;mesothelioma;metalloproteinases;genetic variability;
Podatki
Jezik: |
Angleški jezik |
Leto izida: |
2021 |
Tipologija: |
1.02 - Pregledni znanstveni članek |
Organizacija: |
UL MF - Medicinska fakulteta |
UDK: |
616-006 |
COBISS: |
74658819
|
ISSN: |
2218-273X |
Št. ogledov: |
146 |
Št. prenosov: |
44 |
Ocena: |
0 (0 glasov) |
Metapodatki: |
|
Ostali podatki
Sekundarni jezik: |
Slovenski jezik |
Sekundarne ključne besede: |
mezoteliom;metaloproteinaza;genetska variabilnost; |
Vrsta dela (COBISS): |
Članek v reviji |
Strani: |
str. 1-10 |
Letnik: |
ǂVol. ǂ11 |
Zvezek: |
ǂno. ǂ9 |
Čas izdaje: |
2021 |
DOI: |
10.3390/biom11091272 |
ID: |
14976282 |