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低聚原花青素对人结肠癌细胞系SNU-C4的抗癌作用。

Anticancer effects of oligomeric proanthocyanidins on human colorectal cancer cell line, SNU-C4.

作者信息

Kim Youn-Jung, Park Hae-Jeong, Yoon Seo-Hyun, Kim Mi-Ja, Leem Kang-Hyun, Chung Joo-Ho, Kim Hye-Kyung

机构信息

Department of Food and Biotechnology, Hanseo University, Seosan, South Korea.

出版信息

World J Gastroenterol. 2005 Aug 14;11(30):4674-8. doi: 10.3748/wjg.v11.i30.4674.

Abstract

AIM

Oligomeric proanthocyanidins (OPC), natural polyphenolic compounds found in plants, are known to have antioxidant and anti-cancer effects. We investigated whether the anti-cancer effects of the OPC are induced by apoptosis on human colorectal cancer cell line, SNU-C4.

METHODS

Colorectal cancer cell line, SNU-C4 was cultured in RPMI 1640 medium supplemented with 10% fetal bovine serum. The cytotoxic effect of OPC was assessed by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenylt-etrazolium bromide (MTT) assay. To find out the apoptotic cell death, 4, 6-diamidino-2-phenylindole (DAPI) staining, terminal deoxynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) assay, reverse transcription-polymerase chain reaction (RT-PCR), and caspase-3 enzyme assay were performed.

RESULTS

In this study, cytotoxic effect of OPC on SNU-C4 cells appeared in a dose-dependent manner. OPC treatment (100 microg/mL) revealed typical morphological apoptotic features. Additionally OPC treatment (100 microg/mL) increased level of BAX and CASPASE-3, and decreased level of BCL-2 mRNA expression. Caspase-3 enzyme activity was also significantly increased by treatment of OPC (100 microg/mL) compared with control.

CONCLUSION

These data indicate that OPC caused cell death by apoptosis through caspase pathways on human colorectal cancer cell line, SNU-C4.

摘要

目的

低聚原花青素(OPC)是植物中发现的天然多酚化合物,已知具有抗氧化和抗癌作用。我们研究了OPC对人结肠癌细胞系SNU-C4的抗癌作用是否通过凋亡诱导。

方法

将结肠癌细胞系SNU-C4培养于补充有10%胎牛血清的RPMI 1640培养基中。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法评估OPC的细胞毒性作用。为了确定凋亡细胞死亡情况,进行了4,6-二脒基-2-苯基吲哚(DAPI)染色、末端脱氧核苷酸转移酶(TdT)介导的dUTP缺口末端标记(TUNEL)测定、逆转录聚合酶链反应(RT-PCR)和半胱天冬酶-3酶活性测定。

结果

在本研究中,OPC对SNU-C4细胞的细胞毒性作用呈剂量依赖性。OPC处理(100μg/mL)显示出典型的形态学凋亡特征。此外,OPC处理(100μg/mL)增加了BAX和CASPASE-3的水平,并降低了BCL-2 mRNA表达水平。与对照组相比,OPC(100μg/mL)处理也显著增加了半胱天冬酶-3酶活性。

结论

这些数据表明,OPC通过半胱天冬酶途径诱导人结肠癌细胞系SNU-C4凋亡,从而导致细胞死亡。

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