IN VITRO EVALUATION OF ANTIPROLIFERATIVE AND CYTOTOXIC PROPERTIES OF PTEROSTILBENE AGAINST HUMAN COLON CANCER CELLS

被引:0
|
作者
Wawszczyk, Joanna [1 ]
Kapral, Malgorzata [1 ]
Hollek, Andrzej [1 ]
Weglarz, Ludmila [1 ]
机构
[1] Med Univ Silesia, Sch Pharm, Div Lab Med, Dept Biochem, Jednosci 8, PL-41200 Sosnowiec, Poland
来源
ACTA POLONIAE PHARMACEUTICA | 2014年 / 71卷 / 06期
关键词
pterostilbene; colon cancer; proliferation; Caco-2 cell line; CHEMOPREVENTION; CARCINOGENESIS; PATHWAY;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Colon cancer has been remaining the second leading cause of cancer mortality in Poland in the last years. Epidemiological. preclinical and clinical studies reveal that dietary phytochemicals may exert chemopreventive and therapeutic effect against colorectal cancer. There is a growing interest in identifying new biologically active agents from dietary sources in this respect. Pterostilbene (trans-3,5-dimethoxy-4-hydroxystilbene) is a naturally occurring stilbene, that has been found to have antioxidative, anti-inflammatory and antiproliferative properties. Compared to other stilbenes, pterostilbene has greater bioavailability, and so, a greater potential for clinical applications. Recent studies showed that pterostilbene exhibits the hallmark characteristics of an anticancer agent. The aim of this study was to analyze antiproliferative and cytotoxic effects of pterostilbene on human colon cancer Caco-2 cells. They were cultured using standard techniques and exposed to increasing doses of pterostilbene (5-100 mu M) for 48 and 72 h. Cell proliferation was determined by sulforhodamine B assay. The growth of treated cells was expressed as a percentage of that of untreated control cells. Pterostilbene decreased proliferation rate of Caco-2 cells in a dose- and time-dependent manner. Its concentrations = 25 mu M did not affect cell growth after 48 h treatment period. Significant growth inhibition was observed in cultures incubated with higher concentrations of pterostilbene (40-100 mu m). Pterostilbene at all concentrations used (5-100 mu M) caused significant inhibition of cell proliferation when the experimental time period was elongated to 72 h. The maximum growth reduction was observed at 100 mM pterostilbene. The cytotoxicity of pterostilbene was evaluated in 48 h cultures based on lactate dehydrogenase (LDH) leakage into the culture medium and showed dose-related pattern. The findings of this study showed significant dose-dependent antiproliferative and cytotoxic effects of pterostilhene against human colon cancer cells in vitro.
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页码:1051 / 1055
页数:5
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