Hundreds of chemicals used in pesticides linked to increased breast cancer risk
Peer-Reviewed Publication
Updates every hour. Last Updated: 25-Oct-2026 15:15 ET (25-Oct-2026 19:15 GMT/UTC)
Scientists at Silent Spring Institute have identified 485 chemicals used in pesticide products that could increase breast cancer risk. The list includes active ingredients as well as hundreds of so-called “inert” or inactive ingredients, which typically evade safety testing. The findings could inform policies to strengthen how pesticides are regulated in the U.S. and ensure that pesticide formulations are properly evaluated for their potential to cause breast cancer.
An international research partnership is setting out to address a long-standing gap in global health: children weighing less than 15 kg, broadly corresponding to those under five years of age, are affected by the same parasitic diseases targeted by ivermectin-based control programmes, yet are excluded from receiving the drug because there is currently not enough safety evidence to support its use in this age group.
The IVM-KIDS project aims to address that evidence gap. Bringing together eight institutions across Africa and Europe, the four-year initiative will generate the clinical, pharmacological and regulatory evidence needed to determine whether ivermectin can be safely and effectively extended to treat younger children.
If successful, the project could help pave the way for younger children to be included in ivermectin-based programmes targeting several neglected tropical diseases. Children weighing less than 15 kg are estimated to represent around 20% of the population in endemic regions, making this evidence gap relevant not only to individual treatment, but also to the reach and inclusiveness of large-scale parasite control programmes.
In a new study, scientists have made significant progress in developing a robust approach for the identification of chemical hazards using an informed selection of in vitro bioassays.
A retrospective study of 388 patients with immune checkpoint inhibitor (ICI)-related diarrhea finds that low fecal elastase levels often accompany intestinal inflammation yet were associated with similar diarrheal outcomes compared with normal levels. The results suggest low elastase likely reflects stool dilution rather than true pancreatic insufficiency, supporting fecal fat testing before initiating pancreatic enzyme replacement therapy.
Most local anesthetics used in medicine only last eight to 12 hours or a day tops. Now Boston Children’s Hospital researchers have formulated a more effective slow-release injectable drug delivery system that achieved pain-numbing anesthetic effects lasting two to three weeks in rats compared to a commercial formulation lasting about four to eight hours. Given that nerve blocks in humans tend to work longer than in rats, this advancement, published today in Nature Biomedical Engineering, could blow the effective time of currently used anesthetics out of the water and have implications for other types of pain.
Mitochondrial transplantation is emerging as an organelle-level therapeutic strategy for diseases associated with mitochondrial dysfunction. A new Perspective in Science Bulletin discusses how engineered mitochondrial delivery systems may improve mitochondrial stability, targeting, and clinical translation.
What if cells that form scars after a spinal cord injury could become part of the repair process? Researchers have developed a genetic system that converts certain scar-forming cells into neurons, improving movement in mice and rats with spinal cord injuries.
A joint research team led by Director C. Justin LEE of the Center for Memory and Glioscience at the Institute for Basic Science and Professor HA Yoon of Yonsei University College of Medicine developed TRANsCre-DIONE, a system designed to selectively convert reactive astrocytes at an injury site into neurons. The findings offer a potential new direction for spinal cord repair, although the approach has not been tested as a treatment in humans.