Effects of hispolon on glioblastoma cell growth

被引:25
作者
Arcella, Antonietta [1 ]
Oliva, Maria Antonietta [1 ]
Sanchez, Massimo [3 ]
Staffieri, Sabrina [1 ]
Esposito, Vincenzo [1 ,2 ]
Giangaspero, Felice [1 ,2 ]
Cantore, Giampaolo [1 ]
机构
[1] IRCCS INM Neuromed, Pozzilli, Italy
[2] Univ Rome Sapienza, Rome, Italy
[3] ISS, Rome, Italy
关键词
adjuvant chemotherapy; apoptosis; basidiomycete; brain cancer; cell cycle; glioblastoma; hispolon; natural drug; Phellinus linteus; temozolomide; PHELLINUS-LINTEUS; CANCER CELLS; IN-VITRO; POLYSACCHARIDE EXTRACT; MEDICINAL MUSHROOM; SIGNALING PATHWAYS; CYCLE ARREST; APOPTOSIS; PHOSPHORYLATION; THERAPEUTICS;
D O I
10.1002/tox.22419
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hispolon is a polyphenolic compound isolated from Phellinus linteus which exhibits antitumor activity. Here, we explored the effects of hispolon on human glioblastoma cells U87MG. Cell viability was examined by MTT assay. Growth was investigated by incubating cells with various concentrations of hispolon (25 and 50 mu M) for 24, 48 or 72 h and daily cell count. Cell cycle and apoptosis assay were assessed by flow cytometry. Hispolon decreased cell viability in a dose-and time-dependent manner. The cell cycle distribution showed that hispolon enhanced the accumulation of the cells in G2/M phase. Hispolon decreased the expression of G1-S transition-related protein cyclin D4 but increased the expression of CDK inhibitor p21. Additionally, hispolon enhanced the expression of p53. Moreover, hispolon treatment was effective on U87MG cells in inhibiting cell viability and inducing cell apoptosis. Our results indicate that hispolon inhibits the cell viability, induces G2/M cell cycle arrest and apoptosis in glioblastoma U87MG cells, and p53 should play a role in hispolon-mediated antitumor activity.
引用
收藏
页码:2113 / 2123
页数:11
相关论文
共 47 条
[1]  
Abukhdeir Abde M., 2008, Expert Reviews in Molecular Medicine, V10, P1, DOI 10.1017/S1462399408000744
[2]   In vitro and in vivo effect of human lactoferrin on glioblastoma growth [J].
Arcella, Antonietta ;
Oliva, Maria Antonietta ;
Staffieri, Sabrina ;
Alberti, Silvia ;
Grillea, Giovanni ;
Madonna, Michele ;
Bartolo, Marcello ;
Pavone, Luigi ;
Giangaspero, Felice ;
Cantore, Giampaolo ;
Frati, Alessandro .
JOURNAL OF NEUROSURGERY, 2015, 123 (04) :1026-1035
[3]  
Chang H.Y., 2011, EVID-BASED COMPL ALT, V2011
[4]   The apoptosis effect of hispolon from Phellinus linteus (Berkeley & Curtis) Teng on human epidermoid KB cells [J].
Chen, W ;
He, FY ;
Li, YQ .
JOURNAL OF ETHNOPHARMACOLOGY, 2006, 105 (1-2) :280-285
[5]   Hispolon induces apoptosis in human gastric cancer cells through a ROS-mediated mitochondrial pathway [J].
Chen, Wei ;
Zhao, Zhao ;
Li, Ling ;
Wu, Bin ;
Chen, Shi-fei ;
Zhou, Hong ;
Wang, Yong ;
Li, Yong-Quan .
FREE RADICAL BIOLOGY AND MEDICINE, 2008, 45 (01) :60-72
[6]   Hispolon from Phellinus linteus Induces G0/G1 Cell Cycle Arrest and Apoptosis in NB4 Human Leukaemia Cells [J].
Chen, Yi-Chuan ;
Chang, Heng-Yuan ;
Deng, Jeng-Shyan ;
Chen, Jian-Jung ;
Huang, Shyh-Shyun ;
Lin, I-Hsin ;
Kuo, Wan-Lin ;
Chao, Wei ;
Huang, Guan-Jhong .
AMERICAN JOURNAL OF CHINESE MEDICINE, 2013, 41 (06) :1439-1457
[7]   Hispolon Decreases Melanin Production and Induces Apoptosis in Melanoma Cells through the Downregulation of Tyrosinase and Microphthalmia-Associated Transcription Factor (MITF) Expressions and the Activation of Caspase-3,-8 and-9 [J].
Chen, Yi-Shyan ;
Lee, Shu-Mei ;
Lin, Chih-Chien ;
Liu, Chia-Yi .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (01) :1201-1215
[8]   TYROSINE PHOSPHORYLATION IS AN EARLY AND SPECIFIC EVENT INVOLVED IN PRIMARY KERATINOCYTE DIFFERENTIATION [J].
FILVAROFF, E ;
STERN, DF ;
DOTTO, GP .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (03) :1164-1173
[9]   Analysis of drug combinations: current methodological landscape [J].
Foucquier, Julie ;
Guedj, Mickael .
PHARMACOLOGY RESEARCH & PERSPECTIVES, 2015, 3 (03)
[10]   Effects of Ganopoly® (A Ganoderma lucidum polysaccharide extract) on the immune functions in advanced-stage cancer patients [J].
Gao, YH ;
Zhou, SF ;
Jiang, WQ ;
Huang, M ;
Dai, XH .
IMMUNOLOGICAL INVESTIGATIONS, 2003, 32 (03) :201-215