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PMID: 23195226 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Induction of a trophoblast-like phenotype by hydralazine in the p19 embryonic carcinoma cell line.

Biochimica et biophysica acta ·Vol. 1833 ·No. 3 ·2013-03-00 ·页码 460-7

O'Driscoll CM, Coulter JB, Bressler JP

Abstract

Chemicals that affect cellular differentiation through epigenetic mechanisms have potential utility in treating a wide range of diseases. Hydralazine decreases DNA methylation in some cell types but its effect on differentiation has not been well explored. After five days of exposure to hydralazine, P19 embryocarcinoma cells displayed a giant cell morphology and were binucleate, indicative of a trophoblast-like morphology. Other trophoblast-like properties included the intermediary filament Troma-1/cytokeratin 8 and the transcription factor Tead4. A decrease in CpG methylation at three sites in the TEAD4 promoter and the B1 repeated sequence was observed. Knocking down expression of Tead4 with siRNA blocked the increase in Troma-1/cytokeratin 8 and over expression of Tead4 induced the expression of Troma-1/cytokeratin 8. Cells treated for 5days with hydralazine were no longer capable of undergoing retinoic acid-mediated neuronal differentiation. An irreversible loss of the pluripotent transcription factor Oct-4 was observed following hydralazine exposure. In summary, hydralazine induces P19 cells to assume a trophoblast-like phenotype by upregulating Tead4 expression through a mechanism involving DNA demethylation.

MeSH 主题词
Animals Apoptosis/drug effects Blotting, Western Cell Differentiation/drug effects Cell Proliferation/drug effects DNA Methylation/drug effects DNA-Binding Proteins/genetics,metabolism Embryonal Carcinoma Stem Cells/drug effects,metabolism,pathology Gene Expression Regulation, Developmental/drug effects Hydralazine/pharmacology Immunoenzyme Techniques Keratin-8/genetics,metabolism Mice Muscle Proteins/genetics,metabolism Neurons/metabolism,pathology Phenotype RNA, Messenger/genetics Real-Time Polymerase Chain Reaction Reverse Transcriptase Polymerase Chain Reaction TEA Domain Transcription Factors Transcription Factors/genetics,metabolism Tretinoin/pharmacology Trophoblasts/drug effects,metabolism,pathology Tumor Cells, Cultured
化学物质
DNA-Binding Proteins Keratin-8 Muscle Proteins RNA, Messenger TEA Domain Transcription Factors Tead4 protein, mouse Transcription Factors Hydralazine Tretinoin
作者与单位
共 3 位作者,点击展开单位 / ORCID
O'Driscoll Cliona M
Division of Toxicological Sciences, Department of Environmental Health Sciences, Johns Hopkins Bloomberg School of Public Health and Hugo Moser Research Institute at Kennedy Krieger, Baltimore, MD 21205, USA. [email protected]
Coulter Jonathan B
Bressler Joseph P
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Corresponding email
Published
2013-03-00
电子出版
2012-00-26
页码
460-7
Language
English
Country/Region
Netherlands
NLM ID
0217513
基金资助
NICHD NIH HHS · HD24448 · United States
NIEHS NIH HHS · ES07141 · United States
NIEHS NIH HHS · R41 ES020659 · United States
NICHD NIH HHS · P01 HD024448 · United States
NIEHS NIH HHS · T32 ES007141 · United States
NIEHS NIH HHS · P30 ES003819 · United States
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