A polysaccharide from Trametes robiniophila Murrill induces apoptosis through intrinsic mitochondrial pathway in human osteosarcoma (U-2 OS) cells

被引:12
|
作者
Zhao, Xingkai [1 ]
Ma, Shuo [1 ]
Liu, Ning [1 ]
Liu, Jiakun [1 ]
Wang, Wenbo [1 ]
机构
[1] Harbin Med Univ, Dept Orthopaed Surg, Affiliated Hosp 1, Harbin 150001, Peoples R China
关键词
Trametes robiniophila; Polysaccharide; Osteosarcoma; Apoptosis; MTDH; ELEVATED GENE-1 AEG-1; INHIBITS PROLIFERATION; PEDIATRIC OSTEOSARCOMA; PROGNOSTIC-FACTORS; CYTOCHROME-C; BCL-2; FAMILY; DEATH; SURVIVAL; BAX; EXTRACT;
D O I
10.1007/s13277-015-3185-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this study, we isolated and purified one homogeneous polysaccharide (TRP) from the fruiting bodies of Trametes robiniophila Murrill, and its average molecular weight was estimated to be 8.7x10(4) Da. Monosaccharide composition analysis by gas chromatography (GC) indicated that TRP was composed of glucose, galactose, and arabinose in the molar ratio of 4.2:1.10:1.06. Particularly, we evaluated the anti-cancer efficacy of TRP on human osteosarcoma U-2 OS cells in vitro and associated possible molecular mechanism. Our result provided the first evidence that treatment of U-2 OS cells with TRP resulted in a dose-and time-dependent inhibitory effect on cell proliferation of U-2 OS cells and caused apoptotic death. Moreover, TRP induced the apoptosis of U-2 OS cells via a mitochondria-dependent pathway, as evidenced by an increase in Bax/Bcl-2 ratio, a loss of mitochondrial membrane potential (Delta psi m), release of cytochrome c from the mitochondria to the cytosol, activation of caspase-9 and caspase-3, and cleavage of poly(ADP-ribose) polymerase (PARP) in U-2 OS cells. In addition, overexpression of metadherin (MTDH), one carcinogene, was inhibited in U-2 OS cells after exposure to TRP for 24 h. Our findings suggested that TRP inhibited the proliferation of human osteosarcoma cancer cells by promoting apoptosis through the intrinsic mitochondrial pathway, as well as inhibition of MTDH expression.
引用
收藏
页码:5255 / 5263
页数:9
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