In Vitro Assessment of the Cytotoxic, Apoptotic, and Mutagenic Potentials of Isatin

被引:14
作者
Candido-Bacani, Priscila de Matos [1 ]
Mori, Mateus Prates [1 ]
Calvo, Tamara Regina [2 ]
Vilegas, Wagner [2 ]
Varanda, Eliana Aparecida [3 ]
de Syllos Colus, Ilce Mara [1 ]
机构
[1] Univ Estadual Londrina, Dept Gen Biol, Ctr Biol Sci, Londrina, PR, Brazil
[2] Sao Paulo State Univ, Araraquara Inst Chem, Araraquara, SP, Brazil
[3] Sao Paulo State Univ, Araraquara Fac Pharmaceut Sci, Dept Biol Sci, Araraquara, SP, Brazil
来源
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | 2013年 / 76卷 / 06期
关键词
CELL LINE; ANTICANCER; ERK; IDENTIFICATION; COMPLEXES;
D O I
10.1080/15287394.2012.755941
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Isatin (1H-indole-2,3-dione) is a chemical found in various medicinal plant species and responsible for a broad spectrum of pharmacological and biological properties that may be beneficial to human health, as an anticonvulsant, antibacterial, antifungal, antiviral, and anticancer agent. The aim of the present study was to determine in vitro the cytotoxic, mutagenic, and apoptotic effects of isatin on CHO-K1 and HeLa cells using the MTT viability assay (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide), micronucleus (MN) test, apoptosis index, and nuclear division index (NDI). The 5 isatin concentrations evaluated in the mutagenicity and apoptosis tests were 0.5, 1, 5, 10, and 50 M, selected through a preliminary MTT assay. Positive (doxorubicin, DXR) and negative (phosphate buffered saline, PBS) control groups were also included in the analysis. Isatin did not exert a mutagenic effect on CHO-K1 after 3 and 24 h of treatment or on HeLa cells after 24 h. However, 10 and 50 M concentrations inhibited cell proliferation and promoted apoptosis in both CHO-K1 and HeLa cells. Data indicate that the cytotoxic, apoptotic, and antiproliferative effects of isatin were concentration independent and cell line independent.
引用
收藏
页码:354 / 362
页数:9
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