Dichlormethane Extract of the Jelly Ear Mushroom Auricularia auricula-judae (Higher Basidiomycetes) Inhibits Tumor Cell Growth In Vitro

被引:25
作者
Reza, Md Ahsanur [1 ]
Hossain, Md Akil [1 ]
Lee, Seung-Jin [1 ]
Yohannes, Sileshi Belew [1 ]
Damte, Dereje [1 ]
Rhee, Man-Hee [1 ]
Jo, Woo-Sik [2 ]
Suh, Joo-Won [3 ]
Park, Seung-Chun [1 ]
机构
[1] Kyungpook Natl Univ, Coll Vet Med, Taegu 702701, South Korea
[2] Gyeongbuk Agr Technol Adm, Agr Environm Dept, Taegu, South Korea
[3] Myongji Univ, Ctr Nutraceut & Pharmaceut Mat, Div Biosci & Bioinformat, Yongin, Gyeonggi, South Korea
关键词
medicinal mushrooms; Auricularia auricula-judae; GC-MS; dichloromethane fraction; antitumor; antioxidant; COMPARATIVE ANTITUMOR-ACTIVITY; MEDICINAL MUSHROOM; CANCER; APOPTOSIS; PROLIFERATION; ANTIOXIDANT; INDUCTION; AGENTS; BCL-2;
D O I
10.1615/IntJMedMushr.v16.i1.40
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, a dichloromethane fraction (DCMF) from 70% Auricularia auricula-judae ethanol extract showed the highest level of antitumor activity compared to other solvent fractions (ethyl acetate, butanol, and water). The DCMF was found to have more potent antitumor activity against broncheoalveolar cancer (half maximal inhibitory concentration = 57.2 mu g/mL) and gastric cancer cells (half maximal inhibitory concentration = 73.2 mu g/mL) compared to the other solvent fractions, although all fractions inhibited the proliferation of the tumor cells in a dose-dependent manner. We further analyzed the DCMF composition by gas chromatography coupled mass spectroscopy. Based on the results of this analysis, an antitumor active component (diazane) was identified in the DCMF. However, we found that diazane alone had a lower level of antitumor activity than the DCMF. These findings indicate that other unknown components of the DCMF also are responsible for the cytotoxic effects of DCMF against tumor cells. Semiquantitative reverse transcription polymerase chain reaction analysis demonstrated that DCMF induced cytotoxicity or tumor cell apoptosis as a result of the downregulation of Bcl-2 expression and p53 overexpression. Taken together, our study results demonstrated that the DCMF may be used as a functional additive for enhancing antioxidant activities and suppressing tumor growth in the body.
引用
收藏
页码:37 / 47
页数:11
相关论文
共 34 条
[1]  
Alam N., 2011, Australian Journal of Basic and Applied Sciences, V5, P229
[2]  
Alberts DS, 1999, CANCER RES, V59, P4743
[3]   A New View of the Lethal Apoptotic Pore [J].
Basanez, Gorka ;
Soane, Lucian ;
Hardwick, J. Marie .
PLOS BIOLOGY, 2012, 10 (09)
[4]   In Vitro Antioxidant and Anti-Inflammatory Activities of Protocatechualdehyde Isolated from Phellinus gilvus [J].
Chang, Zhi-Qiang ;
Gebru, Elias ;
Lee, Sam-Pin ;
Rhee, Man-Hee ;
Kim, Jong-Choon ;
Cheng, Henrique ;
Park, Seung-Chun .
JOURNAL OF NUTRITIONAL SCIENCE AND VITAMINOLOGY, 2011, 57 (01) :118-122
[5]   Synthesis of gibberellin derivatives with anti-tumor bioactivities [J].
Chen, Jingbo ;
Sun, Zhuxian ;
Zhang, Yanli ;
Zeng, Xianghui ;
Qing, Chen ;
Liu, Jianping ;
Li, Liang ;
Zhang, Hongbin .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (18) :5496-5499
[6]   OXIDATIVE DNA-DAMAGE - THE EFFECTS OF CERTAIN GENOTOXIC AND OPERATIONALLY NONGENOTOXIC CARCINOGENS [J].
CLAYSON, DB ;
MEHTA, R ;
IVERSON, F .
MUTATION RESEARCH, 1994, 317 (01) :25-42
[7]  
EMANUEL NM, 1976, CANCER TREAT REP, V60, P1601
[8]  
Fadeyi O, 2004, AFR J BIOTECHNOL, V3, P426
[9]   Accelerated degradation of cellular FLIP protein through the ubiquitin-proteasome pathway in p53-mediated apoptosis of human cancer cells [J].
Fukazawa, T ;
Fujiwara, T ;
Uno, F ;
Teraishi, F ;
Kadowaki, Y ;
Itoshima, T ;
Takata, Y ;
Kagawa, S ;
Roth, JA ;
Tschopp, J ;
Tanaka, N .
ONCOGENE, 2001, 20 (37) :5225-5231
[10]  
Giaccone G, 2002, LUNG CANCER-J IASLC, V38, pS29