A new approach to studying the effects of two common chemicals used in cosmetics and sunscreens found they can cause DNA damage in breast cells at surprisingly low concentrations, while the same dose did not harm cells without oestrogen receptors.
The research, published in Environmental Health Perspectives, identifies a new mechanism by which oestrogens and xenoestrogens – environmental chemicals that act like oestrogens – may promote breast cancer, says breast cancer researcher D. Joseph Jerry, professor of veterinary and animal sciences at the University of Massachusetts Amherst, USA.
“The new research offers more sensitive tools to screen for the potential deleterious effects of environmental chemicals, which would be overlooked by methods currently used,” Jerry explains.
He notes that federal agencies, such as the Food and Drug Administration (FDA), typically screen for toxicity of these chemicals in cell lines that don’t have oestrogen receptors.
The two compounds – examined in cells grown in the lab and in the mammary glands of mice – were the ultraviolet filter benzophenone-3 (BP-3), also known as oxybenzone, and propylparaben (PP), an antimicrobial preservative found in cosmetics and other personal care products.
Jerry emphasises that more research is needed to determine what this discovery may mean in terms of consumer guidelines. “Benzophenone-3 is a sunscreen that works. If you use it, you can prevent skin cancer. Am I arguing you shouldn’t use sunscreen? I am not. But there may be a subset of people for whom it may present a significant hazard,” says Jerry, such as women at high risk for breast cancer or those with a history of oestrogen receptor-positive breast cancer.
Previous research on the impact of BP-3 and PP focused on the exposure necessary to activate specific genes in cancer cells or accelerate their growth. “Those effects required concentrations that exceed the levels that most women are normally exposed to,” Jerry says.
But the new research shows that DNA damage in breast cells with oestrogen receptors occurred at concentrations that are 1/10th to 1/30th of that required to stimulate proliferation or gene expression.
“There may be a risk at lower levels than we would have previously understood,” Jerry says.
Jerry and colleagues at UMass Amherst, UMass Medical Center-Baystate and Pioneer Valley Life Sciences Institute decided to look at whether PP and BP-3 have oestrogenic effects at concentrations relevant to population exposures because “we know that oestrogen can promote breast cancer,” Jerry says.
“It’s not toxic unless the cells have oestrogen receptors,” he says. “So it’s acting through the oestrogen receptor to create this damage. There is no consequence if you test it in other cells.”