Novel effect and the mechanistic insights of fruiting body extract of medicinal fungus Antrodia cinnamomea against T47D breast cancer

Phytomedicine ◽  
2017 ◽  
Vol 24 ◽  
pp. 39-48 ◽  
Author(s):  
Kuang-Ming Shang ◽  
Tzu-Hsuan Su ◽  
Wai Leng Lee ◽  
Wen-Wei Hsiao ◽  
Ching-Yi Chiou ◽  
...  
2018 ◽  
Vol 6 (6) ◽  
pp. e00027-18 ◽  
Author(s):  
Shu-Ting Cho ◽  
Chia-Ling Chen ◽  
Yin Yang ◽  
Ting-Fang Wang ◽  
Chih-Horng Kuo

ABSTRACTBurkholderia sp. strain WAC0059 was isolated from a fruiting body of the medicinal fungus Antrodia cinnamomea collected in Taiwan. Here, we report the draft genome sequence of this bacterium to facilitate the investigation of its biology.


2014 ◽  
Vol 1 (1) ◽  
pp. 32
Author(s):  
Ross Nurul Rohmah ◽  
Nuniek Ina Ratnaningtyas ◽  
Ari Asnani

Ganoderma lucidum is polyporus fungi from Basidiomycetes which can be used as traditional medicines. Toxicity test with Brine Shrimp Lethality Test (BST) method using Artemia salina was conducted to find out toxic effect of G.lucidum. An extract would have toxic effect if the LC50 < 1000 µg/ml. The aims of this experiment were to know about the toxicity level from G.lucidum with Brine Shrimp Lethality Test (BST) method and determined the concentration of fruiting body extract of G.lucidum which had the best toxicity effect in LC50. There were two extraction methods used in this experiment, first one stage extraction and then multilevel extraction with hexane, ethyl acetate, and ethanol. Each solvent was made in 1000 ppm, 500 ppm, 250 ppm, and 125 ppm. This process was repeated for three times. This experiment used G.lucidum extract which was tested to A.salina and secunder compound metabolit test from the most toxic G. lucidum was done with phytochemical analysis. The result indicated that fruiting body extract from G.lucidum could kill A.salina because all extract was positively contained alkaloid and terpenoid but negatively contained flavonoid. Fruiting body extract from G.lucidum which had lowest LC50 wass ethyl asetat extract with one stage extraction in concentration 53,70 ppm and highest LC50 was ethanol extract with multilevel extraction in concentration 501,18 ppm.


2014 ◽  
Vol 155 (1) ◽  
pp. 154-164 ◽  
Author(s):  
Tsung-Teng Huang ◽  
Sian-Pu Wu ◽  
Kowit-Yu Chong ◽  
David M. Ojcius ◽  
Yun-Fei Ko ◽  
...  

2020 ◽  
Vol Volume 13 ◽  
pp. 9101-9102
Author(s):  
Yu-Ming Liu ◽  
Yu-Kuo Liu ◽  
Ling-Wei Wang ◽  
Yu-Chuen Huang ◽  
Pin-I Huang ◽  
...  

2019 ◽  
Vol 20 (4) ◽  
pp. 833 ◽  
Author(s):  
Yu-Cheng Chen ◽  
Yi-Chang Liu ◽  
Mohamed El-Shazly ◽  
Tung-Ying Wu ◽  
Jan-Gowth Chang ◽  
...  

Reported cases of breast cancer have skyrocketed in the last decades with recent advances in examination techniques. Brest cancer has become the second leading cause of mortality among women worldwide, urging the scientific community to develop or find new drugs from natural sources with potent activity and a reasonable safety profile to tackle this ailment. Antrodia cinnamomea (AC) is a treasured medicinal fungus which has attracted attention due to its potent hepatoprotective and cytotoxic activities. We evaluated the antiproliferative activity of the ethanol extract of artificially cultured AC (EEAC) on breast cancer cells (T47D cells) in vivo and in vitro. Ethanol extract of artificially cultured AC inhibited T47D cells’ proliferation mediated by cell cycle arrest at G1 phase as well induced autophagy. Immunoblotting assay confirmed that EEAC not only decreased the expression of the cell-cycle-related proteins but also increased the expression of transcription factor FOXO1, autophagic marker LC3 II, and p62. Ethanol extract of artificially cultured AC mediated endoplasmic reticulum stress by promoting the expression of IRE1 (inositol-requiring enzyme 1α), GRP78/Bip (glucose regulating protein 78), and CHOP (C/EBP homologous protein). Apart from previous studies, HDACs (histone deacetylases) activity was inhibited as demonstrated by a cell-free system, immunoblotting, and immunofluorescence assays following EEAC treatment. The in vivo studies demonstrated that EEAC decreased tumor volume and inhibited tumor growth without any significant side effects. High performance liquid chromatography profile demonstrated similar triterpenoids compared to the profile of wild AC ethanol extract. The multiple targets of EEAC on breast cancer cells suggested that this extract may be developed as a potential dietary supplement targeting this debilitating disease.


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