AI agents for oncology: Dresden research team develops system to support clinical decisions
Peer-Reviewed Publication
Updates every hour. Last Updated: 23-Jul-2025 07:11 ET (23-Jul-2025 11:11 GMT/UTC)
New research from USC Dornsife scientists reveals how cells fix dangerous DNA damage in hard-to-repair areas of the genome — a process that, when it goes wrong, can lead to cancer and other life-threating diseases. The researchers discovered that a protein called Nup98 helps coordinate DNA repair by moving broken genetic material out of densely packed regions where fixing it is more prone to errors. Nup98 forms liquid droplets around the damaged DNA, creating a protected space that keeps out the wrong repair tools and helps prevent harmful genetic mistakes. The findings offer new insight into how cells maintain genome stability and may help explain how certain mutations in Nup98 contribute to diseases like acute myeloid leukemia.
Every tumor is unique. This makes it difficult to find the most effective therapy for treatment. The Tumor Profiler Center of the University Hospital Zurich, the University of Zurich, ETH Zurich and the University Hospital Basel has now carried out a study in which nine different molecular biological technologies were used to precisely measure the properties of the tumor in four weeks and enable a precise treatment decision. The study is the first of its kind in the world.
Recent results from the NRG-NSABP B-51/RTOG 1304 clinical study showed that the addition of regional nodal irradiation (RNI) does not decrease the rates of invasive breast cancer recurrence in patients whose positive axillary nodes at presentation convert to negative following neoadjuvant chemotherapy. These results were recently published in the New England Journal of Medicine.