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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290926PMC
http://dx.doi.org/10.3390/toxins12050304DOI Listing

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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.

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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.

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