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Novel Metabolites from the Marine-Derived Fungus Peniophora sp. SCSIO41203 Show Promising In Vitro Antitumor Activity as Methuosis Inducers in PC-3 Cells.

Bin YangSurun ShaoMingyi NieQingqing TieXiaoyan PangXiuping LinXue-Feng ZhouYong-Hong LiuXueni WangYunqiu Li
Published in: Marine drugs (2024)
Two new cytochalasin derivatives, peniotrinins A ( 1 ) and B ( 2 ), three new citrinin derivatives, peniotrinins C-E ( 4 , 5 , 7 ), and one new tetramic acid derivative, peniotrinin F ( 12 ), along with nine structurally related known compounds, were isolated from the solid culture of Peniophora sp. SCSIO41203. Their structures, including the absolute configurations of their stereogenic carbons, were fully elucidated based on spectroscopic analysis, quantum chemical calculations, and the calculated ECD. Interestingly, 1 is the first example of a rare 6/5/5/5/6/13 hexacyclic cytochalasin. We screened the above compounds for their anti-prostate cancer activity and found that compound 3 had a significant anti-prostate cancer cell proliferation effect, while compounds 1 and 2 showed weak activity at 10 μM. We then confirmed that compound 3 exerts its anti-prostate cancer effect by inducing methuosis through transmission electron microscopy and cellular immunostaining, which suggested that compound 3 might be first reported as a potential anti-prostate methuosis inducer.
Keyphrases
  • prostate cancer
  • radical prostatectomy
  • cell proliferation
  • electron microscopy
  • molecular dynamics
  • risk assessment
  • molecular docking
  • cell cycle
  • structure activity relationship
  • monte carlo