Elite immune cells lead the fight against multiple myeloma
Peer-Reviewed Publication
Updates every hour. Last Updated: 22-Jun-2026 03:16 ET (22-Jun-2026 07:16 GMT/UTC)
Researchers from The University of Osaka found that only a small subset of tumor-killing T cells undergoes extensive expansion during immunotherapy for multiple myeloma. By tracking individual cells, the team showed that the T-cell clones that later became dominant had already begun expanding shortly after the treatment started. The findings also suggest that highly proliferative immune cells show lower levels of exhaustion-related markers, offering new insights into why some patients respond better to immunotherapy.
A new University of Waterloo study suggests that dietary vitamin C may help reduce cancer risk linked to nitrates and nitrites commonly found in foods such as cured meats and some vegetables. Using mathematical modelling, researchers examined how these compounds behave during digestion and found that vitamin C can inhibit “nitrosation,” a chemical process in the stomach that produces substances suspected of increasing cancer risk. The model showed that foods naturally containing both nitrates and vitamin C, such as leafy greens, may be less harmful than previously thought, and that vitamin C supplements taken with meals could moderately reduce the formation of cancer‑associated compounds.
Three new Virginia Tech studies are taking aim at tobacco use from different angles — from quitting support to purchasing behavior to policy insights — with a focus on reducing cancer risk and improving health outcomes.
Despite impressive innovations in medicine, most advanced-stage cancers still carry a grim prognosis.
Developing more effective treatments requires a deeper understanding of the cellular processes that drive the formation and growth of common cancers.
Growth factor receptors are well-established drivers of many cancers, and many modern therapies target these receptors effectively.
However, cancers in most patients eventually become resistant to existing drugs.
By identifying new cellular components required for growth factor signaling, researchers have uncovered a new class of therapeutic targets.
The 2026 Gruber Genetics Prize is being awarded to Alan G Hinnebusch, PhD, a Distinguished Investigator at the National Institutes of Health, for his pioneering work that established both the paradigm and the detailed mechanism of translational control that underlies the Integrated Stress Response, a pivotal mechanism whereby eukaryotic cells reprogram protein synthesis under stress.
In a series of forward genetics screens in budding yeast, Hinnebusch identified mutations in the kinase Gcn2, which phosphorylates the key translation initiation factor eIF2, and Gcn4, a key transcription factor that controls genes involved in amino acid biosynthesis.
Hinnebusch demonstrated that the phosphorylation of eIF2 suppresses global protein synthesis and selectively induces the master transcription factor Gcn4. This translational control mechanism is broadly conserved from yeast to humans.
Hinnebusch’s work has led to a greater understanding of how cells respond to stressors such as amino acid starvation and viral infections. Dysregulation of the integrated stress response has been linked to neurodegeneration, metabolic disorders and cancer.
Having surgery for rectal cancer at a hospital accredited by the National Accreditation Program for Rectal Cancer was associated with a significant reduction in cancer remaining at the edges of the tumor site, compared to having the same surgery at a non-accredited hospital.