DNA damaging and apoptotic potentials of Bisphenol A and Bisphenol S in human bronchial epithelial cells.

Abstract:

:DNA damage caused by environmental agents often lead to many chronic diseases, including cancer. The present study aimed to understand the relative toxicity possessed by Bisphenol A (BPA) and Bisphenol S (BPS) on human bronchial epithelial cells (BEAS-2B). The cells were exposed to either BPA or BPS and evaluated for its cytotoxicity, reactive oxygen species (ROS), DNA fragmentation, phosphorylated histone protein (γ-H2AX) and DNA tail damage levels. Further, we also studied DNA damage response (DDR) and caspase-3 mechanisms, to evaluate its mechanism of cell death processes. Exposure with 200 μM of BPA, significantly (p < 0.05) induces caspase-3-mediated cell death by inducing cytotoxicity, ROS, and DNA fragmentation. Higher levels of γ-H2AX and DNA tail damage indicated BPA's DNA damaging potential through an ATM/ATR/Chk1/p53-dependent pathway in BEAS-2B cells. Overall, in vitro data exhibited moderate toxicity for BPS in comparison with BPA suggesting the need for a thorough clinical investigation over its safety profile.

authors

George VC,Rupasinghe HPV

doi

10.1016/j.etap.2018.04.009

subject

Has Abstract

pub_date

2018-06-01 00:00:00

pages

52-57

eissn

1382-6689

issn

1872-7077

pii

S1382-6689(18)30073-5

journal_volume

60

pub_type

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