MicroRNA Expression During Long‐Term Treatment With 3‐MCPD and Glycidol In Vitro

Esters of 3-MCPD and glycidol are food contaminants formed during heat processing. Dietary exposure to these compounds may pose a health risk because their free forms exhibit toxic effects that have been linked to renal cancer and other adverse outcomes. Considering that the role of microRNAs (miRNAs) in the toxicity of these contaminants remains poorly understood in the literature, the aim of this study was to investigate changes in miRNA expression linked to renal carcinogenesis using RT-PCR and to 3-MCPD and glycidol. Tumor (786-0) and non-tumor (HK-2 and HEK-293) renal cell lines were exposed to contaminants for 40 and 80 days at low and high concentrations, respectively. Our results demonstrated that glycidol was more toxic than 3-MCPD in renal cell lines, with IC50 values up to 200 mM for 3-MCPD compared to 7.19 mM for glycidol. Furthermore, we observed up to an 11-fold upregulation of miRNAs associated with renal carcinogenesis and a downregulation of tumor suppressor miRNAs. Our data provide new insights that may be relevant for future studies investigating the mechanisms of renal carcinogenesis induced by 3-MCPD and glycidol.

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Publication Details

Journal
Journal of Applied Toxicology
Published
2025-12-17
DOI
https://doi.org/10.1002/jat.70027
Primary Topic
Carcinogens and Genotoxicity Assessment
Type
article
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article

MicroRNA Expression During Long‐Term Treatment With 3‐MCPD and Glycidol In Vitro

Charles H. Lawrie, María Armesto, Adriana Pavesi Arisseto Bragotto, Renan G. Tivanello
Journal of Applied Toxicology
Carcinogens and Genotoxicity Assessment
article

MicroRNA Expression During Long‐Term Treatment With 3‐MCPD and Glycidol In Vitro

Charles H. Lawrie, María Armesto, Adriana Pavesi Arisseto Bragotto, Renan G. Tivanello
article en

Abstract

Esters of 3-MCPD and glycidol are food contaminants formed during heat processing. Dietary exposure to these compounds may pose a health risk because their free forms exhibit toxic effects that have been linked to renal cancer and other adverse outcomes. Considering that the role of microRNAs (miRNAs) in the toxicity of these contaminants remains poorly understood in the literature, the aim of this study was to investigate changes in miRNA expression linked to renal carcinogenesis using RT-PCR and to 3-MCPD and glycidol. Tumor (786-0) and non-tumor (HK-2 and HEK-293) renal cell lines were exposed to contaminants for 40 and 80 days at low and high concentrations, respectively. Our results demonstrated that glycidol was more toxic than 3-MCPD in renal cell lines, with IC50 values up to 200 mM for 3-MCPD compared to 7.19 mM for glycidol. Furthermore, we observed up to an 11-fold upregulation of miRNAs associated with renal carcinogenesis and a downregulation of tumor suppressor miRNAs. Our data provide new insights that may be relevant for future studies investigating the mechanisms of renal carcinogenesis induced by 3-MCPD and glycidol.

Journal of Applied Toxicology
Ikerbasque (ES), Shanghai University (CN), Universidade Estadual de Campinas (UNICAMP) (BR), University of Oxford (GB), Shanghai Advanced Research Institute (CN), Onkologikoa (ES)
Openalex Percentile: Top 51%
Carcinogens and Genotoxicity Assessment
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MicroRNA Expression During Long‐Term Treatment With 3‐MCPD and Glycidol In Vitro — Charles H. Lawrie, María Armesto, et al. · Journal of Applied Toxicology (2025) | TGRS Research Map | TGRS