Article Publish Status: FREE
Abstract Title:

Bisphenol A (BPA) the mighty and the mutagenic.

Abstract Source:

Toxicol Rep. 2018 ;5:76-84. Epub 2017 Dec 16. PMID: 29854579

Abstract Author(s):

Nasir Jalal, Austin R Surendranath, Janak L Pathak, Shi Yu, Chang Y Chung

Article Affiliation:

Nasir Jalal


Bisphenol A (BPA) is one of the most widely used synthetic compounds on the planet. Upon entering the diet, its highest concentration (1-104 ng/g of tissue) has been recorded in the placenta and fetus. This accumulation of BPA can have many health hazards ranging from the easy to repair single strand DNA breaks (SSBs) to error prone double strand DNA breaks (DSBs). Although the Human liver can efficiently metabolize BPA via glucuronidation and sulfation pathways, however the by-product Bisphenolquinone has been shown to act as a DNA adduct. Low doses of BPA have also been shown to interact with various signaling pathways to disrupt normal downstream signaling. Analysis has been made on how BPA could interact with several signaling pathways such as NFκB, JNK, MAPK, ER and AR that eventually lead to disease morphology and even tumorigenesis. The role of low dose BPA is also discussed in dysregulating Cahomeostasis of the cell by inhibiting calcium channels such as SPCA1/2 to suggest a new direction for future research in the realms of BPA induced disease morphology and mutagenicity.

Study Type : Review
Additional Links
Adverse Pharmacological Actions : Mutagenic : CK(29) : AC(17)

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