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PMID: 1735464 Published · ppublish English Journal Article

Cell growth inhibition by prostaglandin A2 results in elevated expression of gadd153 mRNA.

Experimental cell research ·Vol. 199 ·No. 1 ·1992-03-00 ·Pages 85-9

Choi AM, Fargnoli J, Carlson SG, Holbrook NJ

Abstract

Treatment of Hela cells with prostaglandin A2 (PGA2) resulted in a marked inhibition of cell proliferation which was associated with a significant induction of gadd153 mRNA, a member of a novel class of genes associated with growth arrest and DNA damage. Induction of gadd153 mRNA was specific to prostaglandins capable of arresting cell growth and was dose-dependent with the maximum effect seen at 36 microM PGA2. Induction was rapid, occurring within 2-4 h and reaching a maximum by 8 h. These effects were reversible as removal of PGA2 resulted in a rapid decline in gadd153 mRNA levels coincident with resumption of cell growth. PGA2 induction of gadd153 mRNA was completely prevented by the presence of actinomycin D at a concentration sufficient to block transcription and was partially inhibited (50%) by the protein synthesis inhibitor cycloheximide. The presence of the protein kinase inhibitor 2-aminopurine decreased the PGA2 induction of gadd153 mRNA by greater than 90%, suggesting that cellular kinases play a role in the induction of gadd153 by PGA2. Thus PGA2-mediated growth arrest provides a useful model to further define the role of gadd153 in the negative control of cell growth.

Related Genes
MeSH Terms
2-Aminopurine/pharmacology Base Sequence Blotting, Northern Cell Division/drug effects,genetics Cycloheximide/pharmacology DNA Damage/genetics Dactinomycin/pharmacology Gene Expression Regulation/drug effects HeLa Cells Humans Kinetics Molecular Sequence Data Prostaglandins A/pharmacology RNA, Messenger/biosynthesis,genetics
Chemicals
Prostaglandins A RNA, Messenger Dactinomycin 2-Aminopurine Cycloheximide prostaglandin A2
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Choi A M
Laboratory of Molecular Genetics, National Institute on Aging, Baltimore, Maryland 21224.
Fargnoli J
Carlson S G
Holbrook N J
Article Info
Journal
Experimental cell research
Abbr.
Exp Cell Res
ISSN
0014-4827
Published
1992-03-00
Pages
85-9
Language
English
Region
United States
NLM ID
0373226
Subset
IM
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