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Synthesis, characterization and discovery of multiple anticancer mechanisms of dibutyltin complexes based on salen-like ligands
被引:13
|作者:
Tian, Wei
[1
,2
,3
]
Zhong, Wen
[1
,2
,3
]
Yang, Zengyan
[1
,2
,3
]
Chen, Ling
[1
,2
,3
]
Lin, Shijie
[1
,2
,3
]
Li, Yanping
[1
,2
,3
]
Wang, Yuxing
[1
,2
,3
]
Yang, Peilin
[4
]
Long, Xing
[1
,2
,3
]
机构:
[1] Guangxi Int Zhuang Med Hosp, Nanning 530201, Peoples R China
[2] Guangxi Univ Chinese Med, Guangxi Int Zhuang Med Hosp, Nanning 530201, Peoples R China
[3] Guangxi Inst Ethn Med, Nanning 530201, Peoples R China
[4] Guangxi Univ, Sch Med, Guangxi Key Lab Special Biomed, Nanning 530004, Peoples R China
基金:
中国博士后科学基金;
关键词:
Organotin complex;
Anticancer;
ER stress;
ROS;
DNA damage;
Apoptosis;
STRUCTURAL-CHARACTERIZATION;
DRUG-RESISTANCE;
CELL-DEATH;
IN-VITRO;
CANCER;
BINDING;
APOPTOSIS;
ROLES;
BAX;
D O I:
10.1016/j.jinorgbio.2023.112434
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:
A series of novel dibutyltin complexes based on salen-like ligands (S01-S03) were synthesized and characterized using ultraviolet-visible spectra,infrared spectra, 1H, 13C, and 119Sn nuclear magnetic resonance, high-resolution mass spectrometry, X-ray crystallography, and thermogravimetric analysis. Complex S03 had excel-lent anticancer activity in vitro (IC50 = 1.5 +/- 0.2 mu M in CAL-27 cell lines), which highly activated ROS expression levels and induced apoptosis and cell cycle arrest at the G2/M phase. Interestingly, complex S03 induced cancer cell death through multiple mechanisms (mitochondrial pathway, ER-stress pathway, and DNA damage pathway). This study reveals new mechanisms of organotin complexes and provides new insights into the development of organotin metal complexes as anticancer drugs in the future, and compounds with multiple anticancer mechanisms may be a new strategy for delaying or overcoming drug resistance to chemotherapy and target therapy.
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页数:14
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