UNC Superfund Research Program
The UNC Superfund Research Program (UNC SRP)/NC Center for Environmental Risk Analysis (NC-CERA) seeks to understand the human health and environmental risks associated with exposure to toxic chemicals found at hazardous waste sites. Learn more.
Our research interests include:
- Improving our ability to evaluate risk from low-dose exposures;
- Developing biological markers that indicate when a person has been exposed to a chemical;
- Using a systems biology framework to understand the pathways of environmental disease and how chemicals can cause changes to our DNA;
- Understanding how individuals differ in their susceptibility and risk, and how our genes play a role in the development of disease
- Improving methods to measure chronic exposure and bioavailability of toxic chemicals in the environment
- Evaluating factors that influence toxicity of soil during and after bioremediation
Dr. Rebecca Fry’s research team has identified an underlying biological mechanism by which exposure to cadmium may increase the risk of developing preeclampsia.
Using a highly translational approach, the researchers integrated analyses of human placental tissue with cell culture experiments to demonstrate that cadmium is correlated with the expression of miRNAs that target the transforming growth factor-beta (TGF-β) pathway.
Check out the Winter 2017 issue of the UNC Superfund SCOOP for the latest research highlights, trainee news, research translation and community engagement highlights! Highlighted stories include:
- DNA repair pathways help cells tolerate trace levels of hexavalent chromium
- Elizabeth Martin wins the 2016 NIEHS Wetterhahn Memorial Award
- Advancing the use of community engaged research and citizen science in environmental health
Researchers in Dr. Singleton’s lab (Project 5) have isolated and described two novel polycyclic aromatic hydrocarbon (PAH)-degrading bacteria obtained from contaminated soils of former manufactured gas plant (MGP) sites in NC. These microbes represent specific strains within larger groups of previously uncharacterized bacteria described by the research team as “Pyrene Group 1 (PG1)” and “Pyrene Group 2 (PG2)”, so named due to their initial association with the PAH pyrene.