New multi-disciplinary approach sheds light on the role of mitochondrial DNA mutations in cancer
Peer-Reviewed Publication
Updates every hour. Last Updated: 8-Nov-2025 19:10 ET (9-Nov-2025 00:10 GMT/UTC)
Scientists at St. Jude Children’s Research Hospital explored how mutations in mitochondrial DNA contribute to cancer, the extent of their impact, and when and how they become a factor.
The rapid rise of adults taking GLP-1RA medications (e.g., Wegovy, Ozempic, Mounjaro) in the U.S. (16 million and counting) and around the world has been accompanied by a slew of the drugs’ proclaimed health benefits. Weight loss is a common (and extremely popular) side effect, making GLP-1RAs some of the most exciting weapons in the arsenal for battling the obesity epidemic. Loss of unhealthy visceral fat and improved blood sugar control are just two of the downstream effects of this weight loss, which, in turn, promise their own health benefits.
But what do we really know about the long-term impacts of GLP-1RA medications? Researchers caution us not to get ahead of ourselves when it comes to the logical, though still theoretical, possibilities of how these drugs may influence related health conditions such as cancer.
New research published in Immunity by researchers at the University of Pittsburgh found that, in mice, the toxic tumor environment causes mitochondria to generate reactive oxygen species (ROS) that travel to the nucleus and damage telomeres, driving T cells to a dysfunctional state. By preventing damage to telomeres via a targeted antioxidant, scientists hope to rescue T cell function, opening the door to novel therapies to improve the effectiveness of cancer immunotherapies.
Per- and polyfluoroalkyl substances (PFAS), manmade chemicals that accumulate in the body over time, have been linked to liver disease and cancer, but it is not yet clear how they cause damage. USC researchers used a lab model of the human liver to analyze changes at the cellular level, finding that some PFAS triggered fat accumulation and others caused cell damage linked to cancer. The researchers used spheroids, sophisticated 3D models that recreate the structure of the liver using cells from 10 human donors (five male and five female). They exposed the spheroids to four types of PFAS commonly found at high levels in the blood: perfluorooctanoic acid (PFOA), perfluorohexanesulfonic acid (PFHxS), perfluorooctanesulfonic acid (PFOS) and perfluorononanoic acid (PFNA). Each chemical was tested separately to determine its specific effects on liver cells. After seven days of exposure, the researchers separated the spheroids into individual cells for analysis. They used single-cell RNA sequencing to analyze gene expression and a dye-based method to measure fat buildup in the spheroids under a microscope. All four PFAS interrupted cell signaling and immune functions, but exact changes varied from one chemical to the next. Both PFOA and PFHxs increased fat accumulation—PFOA by causing cells to produce more fat and PFHxS by causing cells to retain fat. Both PFOS and PFNA triggered cancer-related changes in cells, but PFNA had a stronger effect, increasing activity in cellular pathways related to inflammation, oxidative stress and DNA repair. Of the cells exposed to PFNA, 61.3% showed gene changes linked to cancer. The researchers also found that liver cells from male and female donors responded differently to PFAS exposure. PFOA has stronger effects on female liver cells, while PFOS had stronger effects on cells from male donors.
Researchers have uncovered a surprising role for electricity in keeping our body’s protective cell layers healthy.
Researchers reveal that lung cancer cells form direct synapses with neurons to grow and proliferate, opening the door to new therapies that cut the communication lines / publication in ”Nature”