posted on 2014-09-02, 00:00authored byAdélaïde Lerebours, Grant D. Stentiford, Brett P. Lyons, John P. Bignell, Stéphane A. P. Derocles, Jeanette M. Rotchell
Fish
diseases are an indicator for marine ecosystem health since
they provide a biological end-point of historical exposure to stressors.
Liver cancer has been used to monitor the effects of exposure to anthropogenic
pollution in flatfish for many years. The prevalence of liver cancer
can exceed 20%. Despite the high prevalence and the opportunity of
using flatfish to study environmentally induced cancer, the genetic
and environmental factors driving tumor prevalence across sites are
poorly understood. This study aims to define the link between genetic
deterioration, liver disease progression, and anthropogenic contaminant
exposures in the flatfish dab (Limanda limanda).
We assessed genetic changes in a conserved cancer gene, Retinoblastoma (Rb), in association with histological diagnosis
of normal, pretumor, and tumor pathologies in the livers of 165 fish
from six sites in the North Sea and English Channel. The highest concentrations
of metals (especially cadmium) and organic chemicals correlated with
the presence of tumor pathology and with defined genetic profiles
of the Rb gene, from these sites. Different Rb genetic profiles were found in liver tissue near each
tumor phenotype, giving insight into the mechanistic molecular-level
cause of the liver pathologies. Different Rb profiles
were also found at sampling sites of differing contaminant burdens.
Additionally, profiles indicated that histological “normal”
fish from Dogger sampling locations possessed Rb profiles
associated with pretumor disease. This study highlights an association
between Rb and specific contaminants (especially
cadmium) in the molecular etiology of dab liver tumorigenesis.