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Advisor(s)
Abstract(s)
Emerging pollutants, such as pharmaceuticals, may pose a considerable environment risk. Hypocholesterolaemic drugs such as statins are among the most prescribed human pharmaceuticals in western
European countries. In vertebrates, this therapeutic class disrupts the cholesterol synthesis by inhibiting
the enzyme 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMGR), responsible for the limiting step in the
mevalonate pathway. Recently, functional studies have shown that statins competitively inhibit HMGR in
vertebrates and arthropods, two taxa that have diverged over 450 million years ago. Importantly, chronic
simvastatin exposure disrupts crustacean reproduction and development at environmentally relevant
concentrations. Hence, a fundamental question emerges: what is the taxonomic scope of statins-induced
HMGR inhibition across metazoans? Here, we address this central question in a large sampling of metazoans using comparative genomics, homology modelling and molecular docking. Sequence alignment of
metazoan HMGRs allowed the annotation of highly conserved catalytic, co-factor and substrate binding sites, including residues highjacked for statin binding. Furthermore, molecular docking shows that
the catalytic domains of metazoan HMGRs are highly conserved regarding interactions, not only with
HMG-CoA, but also with both simvastatin and atorvastatin, the top prescribed statins in Europe and USA.
Hence, the data indicates that both statins are expected to competitively inhibit metazoan’s HMGRs, and
therefore all metazoan taxa might be at risk. The environmental relevance of these findings are discussed
and research priorities established. We believe that the conceptual framework used in this study can be
applied to other emerging pollutants and assist in the design of toxicity testing and risk assessment.
Description
Keywords
Statins Risk assessment Emerging pollutant In silico Toxicity testing Mode of action (MOA)
Citation
Publisher
Elsevier