Gene Expression Profiling Analysis of Bisphenol A-Induced Perturbation in Biological Processes in ER-Negative HEK293 Cells

被引:16
|
作者
Yin, Rong [1 ]
Gu, Liang [2 ]
Li, Min [2 ]
Jiang, Cizhong [2 ]
Cao, Tongcheng [1 ]
Zhang, Xiaobai [2 ]
机构
[1] Tongji Univ, Dept Chem, Shanghai 200092, Peoples R China
[2] Tongji Univ, Shanghai Key Lab Signaling & Dis Res, Sch Life Sci & Technol, Shanghai 200092, Peoples R China
来源
PLOS ONE | 2014年 / 9卷 / 06期
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
BREAST-CANCER; DNA-DAMAGE; RNA-SEQ; EXPOSURE; RECEPTOR; POPULATION; APOPTOSIS; REVEALS; RISK;
D O I
10.1371/journal.pone.0098635
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bisphenol A (BPA) is an environmental endocrine disruptor which has been detected in human bodies. Many studies have implied that BPA exposure is harmful to human health. Previous studies mainly focused on BPA effects on estrogen receptor (ER)-positive cells. Genome-wide impacts of BPA on gene expression in ER-negative cells is unclear. In this study, we performed RNA-seq to characterize BPA-induced cellular and molecular impacts on ER-negative HEK293 cells. The microscopic observation showed that low-dose BPA exposure did not affect cell viability and morphology. Gene expression profiling analysis identified a list of differentially expressed genes in response to BPA exposure in HEK293 cells. These genes were involved in variable important biological processes including ion transport, cysteine metabolic process, apoptosis, DNA damage repair, etc. Notably, BPA up-regulated the expression of ERCC5 encoding a DNA endonuclease for nucleotide-excision repair. Further electrochemical experiment showed that BPA induced significant DNA damage in ER-positive MCF-7 cells but not in ER-negative HEK293 cells. Collectively, our study revealed that ER-negative HEK293 cells employed mechanisms in response to BPA exposure different from ER-positive cells.
引用
收藏
页数:7
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