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Published on: March 6, 2018
Phenolic Endocrine-Disrupting Chemical Exposure and Systemic Biomarker Variability in Patients with Lung Cancer
Larisa Đurić1, Nataša Milošević1, Maja Milanović1
1Faculty of Medicine, Department of Pharmacy, University of Novi Sad, 21000 Novi Sad, Serbia.
Medicina (Kaunas, Lithuania)
|July 28, 2026
Summary
Environmental exposure to endocrine-disrupting chemicals (EDCs) like BPA and TCS is linked to metabolic and inflammatory changes in advanced lung cancer patients. This human biomonitoring study highlights EDCs
Area of Science:
- Environmental Health
- Oncology
- Toxicology
Background:
- Limited human biomonitoring data exists for endocrine-disrupting chemicals (EDCs) in cancer patients.
- Environmental EDC exposure is a suspected factor in cancer-related biological variability.
Purpose of the Study:
- To assess urinary EDC concentrations in advanced lung cancer patients.
- To investigate associations between EDC exposure and cardiometabolic, hematological, inflammatory, and survival parameters.
Main Methods:
- Included 190 patients with stage IIIB/IV lung cancer.
- Measured urinary bisphenol A (BPA), bisphenol S (BPS), triclosan (TCS), and resorcinol (RCO) using validated methods.
- Employed sex-stratified statistical analyses and regression models adjusted for covariates.
Main Results:
- TCS, BPS, RCO, and BPA were detected at varying frequencies, with TCS being most common.
- Sex-specific exposure patterns were noted, with higher BPA and BPS in females.
- EDC exposure correlated with altered kidney function, liver enzymes, inflammatory markers, and anthropometrics.
- BPA/BPS linked to renal function and inflammation; TCS associated with reduced leukocytes.
- Borderline associations observed between BPA exposure and survival.
Conclusions:
- Provides novel human biomonitoring evidence linking phenolic EDCs to systemic metabolic and inflammatory variability in lung cancer.
- Supports the biological plausibility of EDCs contributing to interindividual heterogeneity in cancer-related physiological responses.