Researchers uncovered how loss of NF1 drives ER+ breast cancer to metastasize to the bone
Peer-Reviewed Publication
This month, we're turning our attention to Breast Cancer Awareness Month, a time dedicated to increasing awareness, supporting early detection, and highlighting the ongoing research shaping the future of breast cancer treatment and prevention.
Updates every hour. Last Updated: 21-Oct-2026 05:15 ET (21-Oct-2026 09:15 GMT/UTC)
A Baylor College of Medicine-led team has uncovered how loss of tumor suppressor neurofibromin (NF1) in estrogen receptor-positive (ER+) breast cancer cells drives the cells’ preference to metastasize to the bone.
Senescence is a state in which stressed cells stop dividing but remain alive. New findings reveal that the underlying process unfolds in distinct stages that depend on the type of drug used, and show how a new class of drugs triggers inflammation. The results point the way to a strategy for tuning therapies to avoid inflammation-promoting side effects, particularly for patients with liposarcoma and ER-positive breast cancer.
Researchers at the Yong Loo Lin School of Medicine, National University of Singapore (NUS Medicine) have identified a ‘master switch’ responsible for driving tumour growth in an aggressive form of breast cancer. Blocking the switch with a targeted drug was also found to reduce cancer cell growth and reduce its spread.