Forskolin and Phorbol 12-myristate 13-acetate modulates the expression pattern of AP-1 factors and cell cycle regulators in estrogen-responsive MCF-7 cells
Autor: | K. M. Kiran Kumar, R. L. Babu, M. Naveen Kumar, S. Chidananda Sharma, Rajeshwari H. Patil, Govindarajan T. Ramesh, K.S. Devaraju |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
lcsh:QH426-470 Cell cycle Phorbol esters Biochemistry Article 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine MCF-7 cells Protein kinase A Molecular Biology Genetics (clinical) Protein kinase C lcsh:R5-920 Forskolin Kinase Chemistry Cell growth Cell Biology Cell biology AP-1 transcription factor lcsh:Genetics 030104 developmental biology 030220 oncology & carcinogenesis Phorbol Signal transduction lcsh:Medicine (General) |
Zdroj: | Genes and Diseases, Vol 6, Iss 2, Pp 159-166 (2019) Genes & Diseases |
ISSN: | 2352-3042 |
Popis: | Activator protein-1 (AP-1) transcription factor is a key component of many signal transduction pathways involved in the regulation of cellular processes and controls rapid responses of mammalian cells when exposed to the variety of stimulus. The phorbol 12-myristate 13-acetate and Forskolin (Fo) are well-known kinase activators/stimulators of Protein Kinase C (PKC) and Protein Kinase A (PKA) respectively. Importantly, these kinases are found to be present in transitional points of many cell signaling pathways, especially those involved in proliferation. The stimulating effect of PKC and PKA on the expression of AP-1 factors in MCF-7 breast cell proliferation is not well characterized. Hence, the role of PKC by PMA treatment and the role of PKA by using Fo in MCF-7 cells is investigated. Where, cells treated with PMA showed increased cell proliferation, while Fo had no effect, but inhibited the PMA induced proliferation. The RT-PCR results showed the PMA induced c-Jun, c-Fos and Fra-1 expressions compared to control and Fo. However, Fo in combination with PMA, inhibit the PMA induced above mRNA expressions where Fo alone has no effect. Western blot studies validated the c-Jun expressions in PMA treated MCF-7 cells. Further, PMA increases the mRNA expression of Cyclin-E1, Cyclin-D1, and CDK-4, whereas Fo decreases their expressions. Thus, mitogenic effect of PMA and inhibitory action of Fo on MCF-7 cells is probably enhanced via activation of AP-1 factors and concomitant action of cell cycle regulators in the downstream singling cascade. Keywords: AP-1 transcription factor, Cell cycle, Forskolin, MCF-7 cells, Phorbol esters |
Databáze: | OpenAIRE |
Externí odkaz: |