# Cytotoxic and Synergistic Effects of Environmentally Relevant Binary Pollutant Mixtures in a Human Lymphoblast Cell Line

**Authors:** Francisco Alejandro Lagunas-Rangel

PMC · DOI: 10.3390/jox16020039 · 2026-02-24

## TL;DR

This study shows that combinations of common environmental pollutants can be more harmful to human cells than individual pollutants, emphasizing the need for better risk assessments.

## Contribution

The study identifies synergistic effects of binary pollutant mixtures at environmentally relevant concentrations in human cells.

## Key findings

- The BPA-DBP combination showed 31% cytotoxicity at 100 nM, indicating strong synergy.
- BADGE-BPA also exhibited similar synergistic effects.
- Reactive oxygen species were partially linked to the observed cytotoxicity in mixtures.

## Abstract

Environmental pollutants are persistent chemicals that pose substantial risks to human health, contributing to global mortality and economic burden. In real-world situations, exposure rarely occurs to single compounds; instead, people are chronically exposed to complex mixtures at low concentrations. However, most regulatory frameworks still rely on single-substance risk assessments, potentially underestimating the hazards associated with combined exposures. This study investigated the cytotoxic interactions of binary mixtures of five environmentally relevant pollutants: bisphenol A (BPA), bisphenol A diglycidyl ether (BADGE), dibutyl phthalate (DBP), di(2-ethylhexyl) phthalate (DEHP), and perfluorooctanoic acid (PFOA), using the human lymphoblast cell line NALM-6. Cells were exposed for 72 h to each compound individually and to all possible binary combinations, reflecting concentrations reported in human plasma or serum. Cell viability was assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, and interactions were analyzed using the Bliss model of independence and two-way analysis of variance (ANOVA). Intracellular reactive oxygen species were measured using the 2′,7′-dichlorodihydrofluorescein diacetate (DCFH-DA) probe to explore the involvement of oxidative stress. Synergistic interactions were observed under specific conditions, although not all statistically identified interactions corresponded to biologically significant effects. The BPA-DBP combination produced the highest cytotoxicity when both pollutants were present at 100 nM (31%), consistent with a strong synergistic effect. A similar pattern was observed for BADGE-BPA. ROS production was partially associated with cytotoxicity in these selected mixtures. Overall, these findings highlight the importance of distinguishing statistical synergy from toxicological relevance.

## Linked entities

- **Chemicals:** bisphenol A (PubChem CID 6623), bisphenol A diglycidyl ether (PubChem CID 2286), dibutyl phthalate (PubChem CID 3026), di(2-ethylhexyl) phthalate (PubChem CID 8343), perfluorooctanoic acid (PubChem CID 9554), 2′,7′-dichlorodihydrofluorescein diacetate (PubChem CID 77718), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (PubChem CID 64965)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** DBP (D-box binding PAR bZIP transcription factor) [NCBI Gene 1628] {aka DABP, taxREB302}, CYP2A6 (cytochrome P450 family 2 subfamily A member 6) [NCBI Gene 1548] {aka CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB}, PFAS (phosphoribosylformylglycinamidine synthase) [NCBI Gene 5198] {aka FGAMS, FGAR-AT, FGARAT, GATD8, PURL}, AHR (aryl hydrocarbon receptor) [NCBI Gene 196] {aka FVH3, RP85, bHLHe76}, CYP2A13 (cytochrome P450 family 2 subfamily A member 13) [NCBI Gene 1553] {aka CPAD, CYP2A, CYPIIA13}, CYP2A7 (cytochrome P450 family 2 subfamily A member 7) [NCBI Gene 1549] {aka CPA7, CPAD, CYP2A, CYPIIA7, P450-IIA4}, ARNT (aryl hydrocarbon receptor nuclear translocator) [NCBI Gene 405] {aka ARNT1, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA}, CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559] {aka CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9}, CYP2D6 (cytochrome P450 family 2 subfamily D member 6 (gene/pseudogene)) [NCBI Gene 1565] {aka CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2}, CYP1A1 (cytochrome P450 family 1 subfamily A member 1) [NCBI Gene 1543] {aka AHH, CP11, CYP1, CYPIA1, P1-450, P450-C}, CYP2E1 (cytochrome P450 family 2 subfamily E member 1) [NCBI Gene 1571] {aka CPE1, CYP2E, P450-J, P450C2E}, CYP1B1 (cytochrome P450 family 1 subfamily B member 1) [NCBI Gene 1545] {aka ASGD6, CP1B, CYPIB1, GLC3A, P4501B1}
- **Diseases:** cancer (MESH:D009369), leukemic (MESH:D007938), deaths (MESH:D003643), myeloid leukemia (MESH:D007951), B-cell leukemia (MESH:D015448), metabolic disorders (MESH:D008659), liver and kidney toxicity (MESH:D056486), injury to (MESH:D014947), hematological toxicity (MESH:D006402), ALL (MESH:D054198), Cytotoxic (MESH:D064420), immune dysfunction (MESH:D007154)
- **Chemicals:** BADGE (MESH:C019273), DEHP (MESH:D004051), DMSO (MESH:D004121), penicillin (MESH:D010406), DCFH-DA (MESH:C029569), ROS (MESH:D017382), epoxy (MESH:D004853), BADGE-2H2O (-), 2',7'-dichlorodihydrofluorescein diacetate (MESH:C110400), Phthalates (MESH:C032279), streptomycin (MESH:D013307), DBP (MESH:D003993), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), lipids (MESH:D008055), BPA (MESH:C006780), water (MESH:D014867), MTT (MESH:C070243), isopropanol (MESH:D019840), CO2 (MESH:D002245), carbohydrates (MESH:D002241), tetrazolium salt (MESH:D013778), PFOA (MESH:C023036), phenol red (MESH:D010637), formazan (MESH:D005562)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** NALM-6 — Homo sapiens (Human), Adult B acute lymphoblastic leukemia, Cancer cell line (CVCL_0092)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13010745/full.md

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Source: https://tomesphere.com/paper/PMC13010745