Prorocentrolide and its analogs, the novel naturally derived antitumor agents, have recently been identified in the dinoflagellate . In the current study, the underlying inhibitory mechanisms of 4-hydroxyprorocentrolide () and prorocentrolide C () on the proliferation of human carcinoma cells were determined. and arrested the cell cycle at the S phase in A549 cells and G2/M phase in HT-29 cells, leading to apoptotic cell death, as determined using fluorescence-activated cell sorting analysis with Annexin V/PI double staining. Apoptosis induced by these compounds was associated with alterations in the expression of cell cycle-regulating proteins (cyclin D1, cyclin E1, CDK2, and CDK4), as well as alterations in the levels of apoptosis-related proteins (PPAR, Bcl-2, Bcl-xl, and survivin). These findings provide new insights into the antitumor mechanisms of 4-hydroxyprorocentrolide and prorocentrolide C and a basis for future investigations assessing prorocentrolide analogs as prospective therapeutic drugs.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290926 | PMC |
http://dx.doi.org/10.3390/toxins12050304 | DOI Listing |
Toxins (Basel)
May 2020
Department of Oceanography, Kunsan National University, Gunsan 54150, Korea.
Prorocentrolide and its analogs, the novel naturally derived antitumor agents, have recently been identified in the dinoflagellate . In the current study, the underlying inhibitory mechanisms of 4-hydroxyprorocentrolide () and prorocentrolide C () on the proliferation of human carcinoma cells were determined. and arrested the cell cycle at the S phase in A549 cells and G2/M phase in HT-29 cells, leading to apoptotic cell death, as determined using fluorescence-activated cell sorting analysis with Annexin V/PI double staining.
View Article and Find Full Text PDFJ Nat Prod
April 2019
Department of Marine Biotechnology , Kunsan National University, 558 Daehak-ro , Gunsan 54150 , South Korea.
Herein, we clarify the structure and relative configurations of two prorocentrolide analogues (1 and 2) isolated from the benthic marine dinoflagellate Prorocentrum lima. The results of NMR spectroscopy show that 1 is prorocentrolide substituted by a hydroxy group at C-4, while the newly isolated compound 2 can be thought of as 1 lacking one ether ring and having one extra double bond. The relative configurations of all stereogenic centers and the configurations of the double bonds in 1 and 2 were determined utilizing ROESY correlations and J-based configuration analysis.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!