2007
DOI: 10.1248/bpb.30.1969
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S-Phase Accumulation of Candida albicans by Anticandidal Effect of Amentoflavone Isolated from Selaginella tamariscina

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Cited by 39 publications
(24 citation statements)
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“…In Candida albicans , it could stimulate the intracellular trehalose accumulation and disrupt the dimorphic transition, which meant a stress response to the component [ 182 ]. Further research on its antifungal mechanism of Candida albicans suggested that this active phytochemical arrested cell cycles during the S-phase and inhibited cell proliferation and division [ 183 ]. The anti-candida activity was proved to be related to apoptotic cell death, which may be associated with the mitochondrial dysfunction.…”
Section: Pharmacologymentioning
confidence: 99%
“…In Candida albicans , it could stimulate the intracellular trehalose accumulation and disrupt the dimorphic transition, which meant a stress response to the component [ 182 ]. Further research on its antifungal mechanism of Candida albicans suggested that this active phytochemical arrested cell cycles during the S-phase and inhibited cell proliferation and division [ 183 ]. The anti-candida activity was proved to be related to apoptotic cell death, which may be associated with the mitochondrial dysfunction.…”
Section: Pharmacologymentioning
confidence: 99%
“…Numerous flavonoids are found in the crude extracts of Selaginella tamariscina that exhibit various pharmacological effects. Amentoflavone markedly arrested cell cycles and induced apoptosis of human breast and cervical cancer cells [21,27,28]. In addition, sumaflavone exerted anti-inflammatory effects by blocking iNOS expression through AP-1 inhibition [29].…”
Section: Discussionmentioning
confidence: 99%
“…Currently, many biflavonoids exhibit bioactive functions, and the mechanisms of such effects have been explored. For example, the amentoflavone derived from Selaginella tamariscina or Torreya nucifera has been shown to not only have potent anti-candidal or anti-SARS-coV activities [ 2 , 3 ], but also exhibits anti-neovascularization by interfering in the interaction of VEGF and VEGFR-1 [ 4 , 5 ]. In addition, 7,7″-dimethoxyagastisflavone (DMGF, the structure was shown as Figure 1A ) has been found to have anti-HSV-1 and -HSV-2 activity [ 6 ], and it can cause the cell death via apoptosis or autophagy [ 7 ].…”
Section: Introductionmentioning
confidence: 99%