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https://ir.csmu.edu.tw:8080/ir/handle/310902500/10992
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Title: | The anti-tumor activity of Antrodia salmonea in human promyelocytic leukemia (HL-60) cells is mediated via the induction of G₁ cell-cycle arrest and apoptosis in vitro or in vivo. |
Authors: | Hseu, YC Lee, CC YC, Chen KJ, Kumar CS, Chen YC, Huang LS, Hsu Huang, HC Yang, HL |
Contributors: | 中山醫學大學 |
Keywords: | Antrodia salmonea;Apoptosis;G(1) cell-cycle arrest;Human promyelocytic leukemia;Xenografted nude mice |
Date: | 2014 |
Issue Date: | 2015-07-02T09:12:59Z (UTC)
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ISSN: | 0378-8741 |
Abstract: | ETHNOPHARMACOLOGICAL RELEVANCE:
The medicinal mushroom Antrodia salmonea has been used as a traditional Chinese medicine and has demonstrated antioxidant and anti-inflammatory effects.
MATERIALS AND METHODS:
In the present study, we examined the anti-tumor activity of the fermented culture broth of Antrodia salmonea (AS) in vitro and in vivo and revealed its underlying molecular mechanism of action.
RESULTS:
Treatment of human promyelocytic leukemia (HL-60) cells with AS (50-150 μg/mL) significantly reduced cell viability and caused G1 arrest via the inhibition of cell-cycle regulatory proteins, including cyclin D1, CDK4, cyclin E, cyclin A, and phosphorylated retinoblastoma protein (p-Rb). Furthermore, AS treatment induced apoptosis, which was associated with DNA fragmentation, followed by a sequence of events, including intracellular ROS generation; mitochondrial dysfunction; Fas ligand activation; cytochrome c release; caspase-3, -8, -9, and PARP activation; and Bcl-2/Bax dysregulation. The results of the in vitro study suggested that AS-induced apoptosis in HL-60 cells was mediated by both the mitochondrial and death receptor pathways. Furthermore, we found that AS treatment was effective in delaying tumor incidence in HL-60 xenografted nude mice and reducing tumor burden.
CONCLUSIONS:
To the best of our knowledge, this is the first report confirming the anti-tumor activity of this potentially beneficial mushroom against human promyelocytic leukemia. |
URI: | https://ir.csmu.edu.tw:8080/ir/handle/310902500/10992 http://dx.doi.org/10.1016/j.jep.2014.03.012 |
Relation: | J Ethnopharmacol. 2014 Apr 28;153(2):499-510. |
Appears in Collections: | [生化微生物免疫研究所] 期刊論文
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