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Anticancer Activity and Mechanism Investigation of Beauvericin Isolated from Secondary Metabolites of the Mangrove Endophytic Fungi

机译:红树林内生真菌次级代谢产物中白霉素的抗癌活性及机理研究

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摘要

One known cyclic peptide, beauvericin, was isolated from the secondary metabolites of mangrove endophytic fungi Fusarium sp. (No. DZ27) in South China Sea. Its structure was determined by spectral analyses and comparisons with reference data from literatures. Beauvericin inhibited growth of KB and KBv200 cells potently with IC50 values of 5.76 +/- 0.55 and 5.34 +/- 0.09 mu M, respectively. Furthermore, beauvericin induced apoptosis through mitochondrial pathway, including decrease of relative oxygen species generation, loss of mitochondrial membrane potential, release of cytochrome c, activation of Caspase-9 and -3, and cleavage of PARP. Additionally, regulation of Bcl-2 or Bax was not involved in the apoptosis induced by beauvericin in KB and KBv200 cells.
机译:从红树林内生真菌镰刀菌(Fusarium sp。)的次生代谢产物中分离出一种已知的环状肽,beauvericin。 (编号DZ27)在南海。通过光谱分析和与文献参考数据的比较来确定其结构。白霉素可有效抑制KB和KBv200细胞的生长,IC50值分别为5.76 +/- 0.55和5.34 +/- 0.09μM。此外,beauvericin通过线粒体途径诱导凋亡,包括减少相对氧的产生,线粒体膜电位的丧失,细胞色素c的释放,Caspase-9和-3的活化以及PARP的裂解。此外,Bcl-2或Bax的调节不参与由beauvericin诱导的KB和KBv200细胞凋亡。

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