Alzheimer’s biomarker P-tau 217 is weak in preclinical studies
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Updates every hour. Last Updated: 26-Oct-2026 12:17 ET (26-Oct-2026 16:17 GMT/UTC)
Scientists have found the first direct evidence of the powerful role our genetic makeup plays in influencing our risk of cancer, with inherited genes interacting with acquired genetic mutations to shape how tumours evolve. The findings could explain why some people are more susceptible to cancer than others in the same environment and suggest that future cancer prevention and screening strategies may need to account more carefully for inherited genetics and population diversity.
A recent study from the University of Chicago shows an engineered bacteria strain may be a powerful approach for improving treatment response in pancreatic cancer.
Chimeric antigen receptor (CAR)-T cell therapy, which reprograms an individual’s immune cells to seek out and destroy certain cancer cells, has revolutionized treatment for blood cancers such as lymphoma. But in some patients, the treatment can cause serious side effects. New research led by investigators at the Mass General Brigham Cancer Institute, the Broad Institute of MIT and Harvard, and Dana-Farber Cancer Institute has shown that patients’ inherited genetic makeup can influence whether they benefit from CAR-T cell therapy or experience toxicity from the treatment. The results are published in Science Immunology.
- KAIST and TheraZyne developed a computational antibody-design approach to target intracellular cancer mutations that are inaccessible to conventional antibodies.
- The engineered antibodies selectively eliminate cancer cells carrying the KRAS G12D mutation while minimizing off-target effects, highlighting their potential as next-generation precision antibody therapeutics.
- The study establishes a new platform for developing personalized antibody therapies against a broad range of difficult-to-treat cancers, with further validation in animal models underway.