UT MD Anderson shares latest research breakthroughs
Peer-Reviewed Publication
Updates every hour. Last Updated: 21-Jun-2026 18:15 ET (21-Jun-2026 22:15 GMT/UTC)
AI-powered atlas uncovered tertiary lymphoid structures as prognostic biomarkers
Research reveals drivers of treatment resistance in KRAS-mutant colorectal cancer and insights on which patients may benefit most from immunotherapy for various cancers
Scientists uncover the molecular pathways involved in blood vessel plaques
Immunotherapy could help treat potentially fatal fungal pneumonias
Direct-to-consumer pharmacies may lower costs for generic prescriptions
Researchers at the Francis Crick Institute and University College London (UCL), funded by Cancer Research UK and the European Research Council (ERC), have identified a 14-protein signature in the blood that can predict lung cancer risk more than five years before diagnosis.
How do different cancer subtypes arise? Do they originate from distinct cells, or from a single multipotent cell capable of differentiating into multiple cell types? This question, debated for decades in cancer biology, is now gaining new insight thanks to the work of the Laboratory of Experimental Pathology (ULiège), in collaboration with researchers from Université Paris Cité and Sorbonne University.
Researchers at The University of Texas MD Anderson Cancer Center have discovered a molecular pathway that drives certain stressed or aging cells to become abnormally active, causing inflammation inside blood vessel plaques. This results in disturbed blood flow and high-risk lesions that can lead to blood clots that cause heart attacks or strokes.
Breast cancer can remain dormant in the bone marrow for decades before reactivating, resulting in cancer relapse. A study published in Bone Research unveils the critical role of Notch2 signaling pathway in promoting this dormant state. The study explains how dormant cancer cells mimic healthy stem cells and activate stress pathways to survive in the bone marrow—paving the way for innovative targeted therapies against dormant cancer cells.