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Novel insights into the role of bisphenol A (BPA) in genomic instability

NAR Cancer 2024 7 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Anastasia Hale, Anastasia Hale, George‐Lucian Moldovan George‐Lucian Moldovan

Summary

This review examines how bisphenol A (BPA), a chemical widely used in polycarbonate and PVC plastics, contributes to genomic instability beyond its well-known effects as an endocrine disruptor. Researchers found evidence that BPA can damage DNA, disrupt cell division, and interfere with DNA repair mechanisms. The findings suggest that BPA exposure may play a role in promoting the kind of genetic damage that can lead to serious cellular dysfunction.

Bisphenol A (BPA) is a phenolic chemical that has been used for over 50 years in the manufacturing of polycarbonate and polyvinyl chloride plastics, and it is one of the highest volume chemicals produced worldwide. Because BPA can bind to and activate estrogen receptors, studies have mainly focused on the effect of BPA in disrupting the human endocrine and reproductive systems. However, BPA also plays a role in promoting genomic instability and has been associated with initiating carcinogenesis. For example, it has been recently shown that exposure to BPA promotes the formation of single stranded DNA gaps, which may be associated with increased genomic instability. In this review, we outline the mechanisms by which BPA works to promote genomic instability including chromosomal instability, DNA adduct formation, ROS production, and estrogen receptor (ER) activation. Moreover, we define the ways in which BPA promotes both carcinogenesis and resistance to chemotherapy, and we provide critical insights into future directions and outstanding questions in the field.

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