Syringic acid induces cancer cell death in the presence of Cu (II) ions via pro-oxidant activity

被引:2
|
作者
Rashedinia, Marzieh [1 ,2 ]
Nasrollahi, Azita [2 ]
Shafaghat, Marzieh [2 ]
Momeni, Shahrzad [2 ]
Iranpak, Forough [3 ,4 ]
Saberzadeh, Jamileh [3 ]
Arabsolghar, Rita [3 ,5 ]
Sabahi, Zahra [1 ]
机构
[1] Shiraz Univ Med Sci, Med Plants Proc Res Ctr, Shiraz, Iran
[2] Shiraz Univ Med Sci, Fac Pharm, Dept Pharmacol & Toxicol, Shiraz, Iran
[3] Shiraz Univ Med Sci, Diagnost Lab Sci & Technol Res Ctr, Sch Paramed Sci, Shiraz, Iran
[4] Islamic Azad Univ Shiraz, Dept Biochem, Shiraz, Iran
[5] Shiraz Univ Med Sci, Sch Paramed Sci, Dept Med Lab Sci, Shiraz, Iran
关键词
Syringic acid; Copper; Iron; Cancer cell; Pro-oxidant; Autophagy; OXIDATIVE STRESS; HYDROGEN-PEROXIDE; DNA PROTECTION; COPPER; MECHANISM; AUTOPHAGY; ANTIOXIDANT; POLYPHENOLS; APOPTOSIS; TOXICITY;
D O I
10.4103/2221-1691.345519
中图分类号
R188.11 [热带医学];
学科分类号
摘要
Objective: To investigate the effects of syringic acid on HEK 293 and HepG2 cells in the absence and presence of exogenous Cu (II) and Fe (II) ions. Methods: The antiproliferative effects of syringic acid on HEK 293 and HepG2 cells in the absence and presence of exogenous Cu (II) and Fe (II) ions were examined by MTT assay. Additionally, colony-forming, reactive oxidative species (ROS) generation, apoptosis induction, autophagy, mitochondrial membrane potential, and mitochondrial mass were investigated. Results: At 24 and 72 h, no significant differences were observed in the viability of HepG2 cells between the control and syringic acid + Fe (II) groups. However, exposure of HepG2 cells to syringic acid + Cu (II) for 72 h reduced the cell viability significantly. Furthermore, ROS formation, induction of apoptosis, and autophagic vacuoles were significantly increased in HepG2 cells without marked changes in mitochondrial membrane potential and mitochondrial mass. Moreover, syringic acid + Cu (II) reduced the plating efficiency and surviving fraction significantly. Conclusions: The combination of syringic acid with Cu (II) was toxic to cancer cells and showed pro-oxidant activity. In addition, this combination induced autophagy in cancer cells with less cytotoxic effects on normal cells, which is a potential candidate for the development of novel therapeutics towards cancer.
引用
收藏
页码:270 / 278
页数:9
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