Rhodium (II) complex with 2-benzoylpyridine, a novel potential chemotherapeutic drug, induces cell cycle arrest and apoptosis in HepG2 cells

被引:9
作者
Wang, Xuehong [1 ,2 ,3 ]
Li, Yulan [2 ,3 ]
Lin, Minglin [2 ,3 ]
Jin, Junfei [2 ,3 ]
Huang, Zhaoquan [1 ]
机构
[1] Guilin Med Univ, Affiliated Hosp, Dept Pathol, Guilin 541001, Guangxi, Peoples R China
[2] Guilin Med Univ, Affiliated Hosp, Lab Hepatobiliary & Pancreat Surg, 15 Lequn Rd, Guilin 541001, Guangxi, Peoples R China
[3] Guilin Med Univ, China USA Lipids Hlth & Dis Res, Guilin 541001, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Rhodium (II) complex; G1; phase; Apoptosis; Mitochondrial pathway; Death receptor; G-QUADRUPLEX DNA; IN-VITRO; CANCER STATISTICS; INDUCTION; INHIBITION; RH(III); CD95;
D O I
10.1007/s10534-017-0056-4
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
Rhodium (II) complex with 2-benzoylpyridine (Rh(L)(2)Cl-2) is a new, synthetic, active metal-complex, which is produced by the reaction of 2-benzoylpyridine (L) with rhodium chloride hydrate (RhCl3 center dot nH(2)O). The crystal structure was determined by X-ray diffraction which is mono-nuclear. In order to explore the biological properties of the novel complex, a series of studies were performed. The results showed that Rh(L)(2)Cl-2 had the anti-tumor activity in HepG(2) and other cell lines and has been shown to induce G1 cell cycle arrest and apoptosis in HepG(2) cells. The anti-cancer effect of Rh(L)(2)Cl-2 is regulated by increased expression of caspase-3 and PARP via the mitochondrial and the death receptor pathways. Bcl-2 family proteins might play an important role in the Rh(L)(2)Cl-2-induced changes in these two pathways. Further studies indicated that Rh(L)(2)Cl-2 increased the level of reactive oxygen species (ROS), but that Rh(L)(2)Cl-2-induced apoptosis was ROS-independent. In conclusion, Rh(L)(2)Cl-2 is a potential new anti-tumor drug, which induces HepG(2) cell death via the mitochondrial and death receptor pathways and has no obvious toxicity to normal liver cell.
引用
收藏
页码:903 / 915
页数:13
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