Could this enzyme help remove “zombie” cells from our tissues?
Peer-Reviewed Publication
Updates every hour. Last Updated: 27-Oct-2026 21:16 ET (28-Oct-2026 01:16 GMT/UTC)
Salk scientists identify two cellular programs linked to age-related dysfunction, ferroptosis and senescence, are mechanistically linked through the enzyme acid ceramidase. The team finds that senescent “zombie” cells are more vulnerable to regulated cell death through ferroptosis and that they can pass that sensitivity on to neighboring cells. The observations suggest acid ceramidase could be a powerful therapeutic target for supporting healthy aging and preventing age-related diseases and disorders such as arthritis, dementia, and cancer.
Tumors can evade immune attack by manipulating the thymus, the organ where T cells are trained. Researchers from Japan discovered that specialized immune cells called plasmacytoid dendritic cells transport tumor antigens to the thymus, promoting immune tolerance to tumors. Disrupting this process in mice enhanced anti-tumor immunity and reduced tumor growth. The findings reveal a previously unrecognized mechanism of tumor immune evasion and identify CCR9 as a potential target for future cancer immunotherapies.
Scientists have identified a new mechanism by which mitochondria, the powerhouses inside cells, communicate to cell nuclei to program changes in gene expression in neurons supporting brain development.
The team’s study, published in Science and led by researchers at Brown University and the Children’s Medical Center Research Institute at U.T. Southwestern, reveals that a deficiency in a particular metabolite in the nucleus is a key mechanism underlying the genetic disorder GPT2 deficiency.
All cells in the human body – and the motions they enable, from our beating hearts to our wiggling toes – use energy generated by a molecule called ATP. Its energy is thought to be released to fuel cellular processes in only one way: when ATP’s decomposition is initiated by an enzyme, a specific type of protein. Those natural enzymes are called ATPases, and ATP’s reliance on their activity makes these catalysts a desirable model for drug discovery. For example, a naturally derived ATPase that’s smaller and more malleable than a protein could be designed for a precise job like directing ATP’s energy toward killing cancer cells, or targeted to block the release of energy that stimulates harmful cellular processes. Researchers at The Ohio State University have gotten one step closer to that possibility by identifying the first noncoding RNA derived from human cells that can bind to ATP.
A nationwide randomized clinical trial found that 28.4% of patients receiving 6 months of telehealth counseling and nicotine replacement therapy during cancer treatment were tobacco-free after 6 months, compared with 14.7% of patients referred to a Quitline without further support. The comprehensive approach, delivered through community oncology settings, achieved high participation (81% versus 5%), strong medication use (83% versus 49.5%), and high patient satisfaction (90% versus 40%). The results of this study by the ECOG-ACRIN Cancer Research Group demonstrate that integrating evidence-based, sustained tobacco treatment into routine cancer care is both feasible and highly effective.