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Changes in mammary histology and transcriptome profiles by low-dose exposure to environmental phenols at critical windows of development

Gopalakrishnan, Kalpana, Teitelbaum, Susan L., Lambertini, Luca, Wetmur, James, Manservisi, Fabiana, Falcioni, Laura, Panzacchi, Simona, Belpoggi, Fiorella, Chen, Jia
Environmental Research 2017 v.152 pp. 233-243
DNA replication, adipogenesis, animal models, breast neoplasms, carcinogenesis, cell cycle, cholesterol, chronic exposure, genes, histology, lactation, mammary development, mammary glands, microarray technology, personal care products, phenols, puberty, rats, risk, transcriptome
Exposure to environmental chemicals has been linked to altered mammary development and cancer risk at high doses using animal models. Effects at low doses comparable to human exposure remain poorly understood, especially during critical developmental windows. We investigated the effects of two environmental phenols commonly used in personal care products – methyl paraben (MPB) and triclosan (TCS) – on the histology and transcriptome of normal mammary glands at low doses mimicking human exposure during critical windows of development. Sprague-Dawley rats were exposed during perinatal, prepubertal and pubertal windows, as well as from birth to lactation. Low-dose exposure to MPB and TCS induced measurable changes in both mammary histology (by Masson's Trichrome Stain) and transcriptome (by microarrays) in a window-specific fashion. Puberty represented a window of heightened sensitivity to MPB, with increased glandular tissue and changes of expression in 295 genes with significant enrichment in functions such as DNA replication and cell cycle regulation. Long-term exposure to TCS from birth to lactation was associated with increased adipose and reduced glandular and secretory tissue, with expression alterations in 993 genes enriched in pathways such as cholesterol synthesis and adipogenesis. Finally, enrichment analyses revealed that genes modified by MPB and TCS were over-represented in human breast cancer gene signatures, suggesting possible links with breast carcinogenesis. These findings highlight the issues of critical windows of susceptibility that may confer heightened sensitivity to environmental insults and implicate the potential health effects of these ubiquitous environmental chemicals in breast cancer.