Methylnitrosourea, dimethylbenzanthracene and benzoapyrene differentially affect redox pathways, apoptosis and immunity in zebrafish.
G EğimezerÜ V ÜstündağP S AteşI ÜnalF D ÜstündağA A AlturfanEbru Emekli-AlturfanMeric A AltinözI ElmaciPublished in: Human & experimental toxicology (2020)
Cancer continues to be a major cause of mortality globally. Zebrafish present suitable models for studying the mechanisms of genotoxic carcinogens. The aim of this study was to investigate the interaction between oxidant-antioxidant status, apoptosis and immunity in zebrafish that were exposed to three different genotoxic carcinogens methylnitrosourea, dimethylbenzanthracene, benzoapyrene and methylnitrosourea + dimethylbenzanthracene starting from early embryogenesis for 30 days. Lipid peroxidation, nitric oxide levels, superoxide dismutase and glutathione-S-transferase activities and mRNA levels of apoptosis genes p53, bax, casp3a, casp2 and immunity genes fas, tnfα and ifnγ1 were evaluated. The disruption of the oxidant-antioxidant balance accompanied by altered expressions of apoptotic and immunity related genes were observed in different levels according to the carcinogen applied. Noteworthy, ifnγ expressions decreased in all carcinogen-exposed groups. Our results will provide basic data for further carcinogenesis research in zebrafish models.
Keyphrases
- oxidative stress
- cell death
- anti inflammatory
- cell cycle arrest
- endoplasmic reticulum stress
- nitric oxide
- immune response
- induced apoptosis
- genome wide
- dendritic cells
- hydrogen peroxide
- rheumatoid arthritis
- genome wide identification
- papillary thyroid
- type diabetes
- electronic health record
- cardiovascular disease
- pi k akt
- risk factors
- cell proliferation
- artificial intelligence
- lymph node metastasis