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Cyclic AMP-Epac signaling pathway contributes to repression of PUMA transcription in melanoma cells.
- Source :
-
Melanoma research [Melanoma Res] 2017 Oct; Vol. 27 (5), pp. 411-416. - Publication Year :
- 2017
-
Abstract
- The universal second messenger cAMP regulates numerous cellular processes. Although the cAMP-signaling pathway leads to induction of gene transcription, it remains unknown whether this pathway contributes toward suppression of transcription. Here, we show that blockade of cAMP signaling using MDL12330A led to an increase in PUMA transcript levels, but not p21 in melanoma cells. cAMP downstream component Epac activation was essential for suppression of PUMA transcription as an Epac agonist reversed the effects of MDL12330A. These results suggest that transcriptional repression is one of the functions of the cAMP-Epac signaling pathway.
- Subjects :
- Apoptosis Regulatory Proteins genetics
Cell Line, Tumor
Cyclic AMP antagonists & inhibitors
Cyclin-Dependent Kinase Inhibitor p21 biosynthesis
Cyclin-Dependent Kinase Inhibitor p21 genetics
Guanine Nucleotide Exchange Factors agonists
Guanine Nucleotide Exchange Factors genetics
Humans
Imines pharmacology
Melanoma pathology
Proto-Oncogene Proteins genetics
Second Messenger Systems drug effects
Second Messenger Systems genetics
Skin Neoplasms pathology
Transcription, Genetic drug effects
Apoptosis Regulatory Proteins biosynthesis
Cyclic AMP metabolism
Guanine Nucleotide Exchange Factors metabolism
Melanoma genetics
Melanoma metabolism
Proto-Oncogene Proteins biosynthesis
Skin Neoplasms genetics
Skin Neoplasms metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1473-5636
- Volume :
- 27
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Melanoma research
- Publication Type :
- Academic Journal
- Accession number :
- 28489680
- Full Text :
- https://doi.org/10.1097/CMR.0000000000000363