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Dioxins are persistent environmental pollutants known for their multiple health effects, from skin rashes to liver dysfunction, reproductive toxicity and cancer. While the hazards of dioxins have been well documented, the challenge of developing a comprehensive understanding of the overall health impact of dioxins remains. We propose to address this challenge with a new approach methodology (NAM) consisting of a novel adaptation of the Template-and-Anchor (T&A) modeling paradigm. Generically, the template model is defined as a high-level coarse-grained model capturing the main physiological processes of the system. The variables of this template model are anchor models, which represent component sub-systems in greater detail at lower biological levels. For the case of dioxin, we design the template to capture the systemic effects of dioxin on the body's handling of cholesterol. Two new anchor models within this template elucidate the effects of dioxin on cholesterol transport in the bloodstream and on sex hormone steroidogenesis and the menstrual cycle. A third anchor model, representing dioxin-mediated effects on cholesterol biosynthesis via the mevalonate pathway, had been developed previously. The T&A modeling paradigm enables a holistic evaluation of the impact of toxicants, which in the future may be translated into a powerful tool for comprehensive computational health risk assessments, personalized medicine, and the development of virtual clinical trials.
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http://dx.doi.org/10.1371/journal.pcbi.1012840 | DOI Listing |
Ecotoxicol Environ Saf
September 2025
Department of Urology, Urology Research Institute, the First Affiliated Hospital, Fujian Medical University, Fuzhou 350005, China; Department of Urology, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou 350212, China; Fujian Key Labo
Objective: Polychlorinated dibenzo-p-dioxins (PCDDs) present a significant long-term threat to human health attributable to their toxicological properties, chemical stability and propensity for bioaccumulation. This study seeks to explore the correlation between PCDDs exposure and prostate cancer (PCa) through comprehensive analysis.
Methods: The multi-dimensional analysis was conducted based on various online databases.
Cancer Discov
September 2025
University of Michigan-Ann Arbor, Ann Arbor, MI, United States.
Although smoking is a risk factor for pancreatic adenocarcinoma (PDAC), the underlying mechanism promoting tumorigenesis and progression are unknown. Here, we show that aryl hydrocarbon receptor ligands found in cigarette smoke, like the carcinogen 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), promote pancreatic dysplasia and PDAC progression in a mouse model of this disease. This effect is mediated by AhR activation in CD4+ T cells, leading to their polarization to interleukin-22 (IL22) producing TH22 cells and to regulatory T cells (Treg) accumulation, ultimately driving a blunted CD8+ T cell effector response.
View Article and Find Full Text PDFChemosphere
September 2025
Department of Environmental Health Sciences, School of Public Health, University of Alabama at Birmingham, 1665 University Boulevard, Birmingham, AL, 35294, USA. Electronic address:
Organic contaminants, such as polybrominated diphenyl ethers, dioxins, furans, pesticides, and per- and polyfluoroalkyl substances, have the propensity to cause human and environmental harm, and many of these are currently ubiquitous in the environment. Evaluations of factors influencing the environmental fates and hazard potentials of these organics are accomplished using multimedia models. Climate conditions, land use, and chemical properties are among those factors.
View Article and Find Full Text PDFRes Sq
August 2025
Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.
Environmental exposures to toxic chemicals can profoundly alter the transcriptome and epigenome in both humans and animals, contributing to disease development across the lifespan. To elucidate how early-life exposure to toxicants exerts such persistent effects, the Consortium generated a landmark resource comprising 2,570 epigenomes and 1,043 transcriptomes from longitudinal studies in mice. All data are publicly available through the TaRGET II data portal and the WashU Epigenome Browser.
View Article and Find Full Text PDFEnviron Sci Technol
August 2025
CAS Key Laboratory of Separation Sciences for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, Liaoning 116023, China.
The catalytic mechanisms underlying the formation of polybrominated dibenzo--dioxins and dibenzofurans (PBDD/Fs) have emerged as a critical environmental concern, particularly regarding the roles of metal- and metalloid-based catalysts. Although these catalysts are recognized as crucial agents for the formation of PBDD/Fs, there is still significant knowledge gaps in identifying the active species and quantifying their catalytic activities. This study systematically investigates four key reaction pathways governing PBDD/Fs formation: aromatic bromination, the Deacon reaction, the precursor, and the de novo synthesis process.
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