Effects of bisphenol A on the proliferation and cell cycle of HBL-100 cells
► BPA has estrogen-like activity. ► BPA can stimulate HBL-100 proliferation and cell division through ER pathway. ► BPA may have other pathways that stimulate cell proliferation and cell cycle change. Bisphenol A (BPA) is an environmental estrogen that exhibits non-genotoxic carcinogenicity, causing...
Saved in:
Published in | Food and chemical toxicology Vol. 50; no. 9; pp. 3100 - 3105 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Elsevier Ltd
01.09.2012
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | ► BPA has estrogen-like activity. ► BPA can stimulate HBL-100 proliferation and cell division through ER pathway. ► BPA may have other pathways that stimulate cell proliferation and cell cycle change.
Bisphenol A (BPA) is an environmental estrogen that exhibits non-genotoxic carcinogenicity, causing concern globally. The aim was to investigate the effects of BPA on the proliferation and cell cycle of human normal breast cells HBL-100. An improved E-Screen assay was used to study cell proliferation, and flow cytometry was used to study cell cycle phases. Western blot analysis was utilized to detect cell cycle proteins and estrogen receptor α (ERα) expression. The results showed that the highest cell proliferation rate induced by BPA was at 1.0×10−6mol/L. At 1.0×10−10, 1.0×10−8, and 1.0×10−6mol/L, BPA promoted more cells to enter into G2/M phase and caused an increase in the expression of cyclinD1 and CDK4. After adding ICI182780 into the system, the promoting effects of BPA on cell proliferation and cell cycle change decreased, but these promoting effects were still significantly greater compared with the solvent control (P<0.05). Regardless of ICI182780 exposure, BPA did not have significant effect on ERα expression. BPA has estrogen-like activity and can stimulate HBL-100 proliferation and cell division through the estrogen receptor pathway. BPA may have other pathways through which it can exert stimulating effects and exhibit non-genotoxic carcinogenicity. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0278-6915 1873-6351 |
DOI: | 10.1016/j.fct.2012.06.029 |