Chloroform fraction of Scutellaria barbata D. Don inhibits the growth of colorectal cancer cells by activating miR-34a

被引:33
作者
Zhang, Ling [1 ,2 ]
Fang, Yi [1 ,2 ]
Feng, Jian-Yu [1 ,2 ]
Cai, Qiao-Yan [1 ,2 ]
Wei, Li-Hui [1 ,2 ]
Lin, Shan [1 ,2 ]
Peng, Jun [1 ,2 ]
机构
[1] Fujian Univ Tradit Chinese Med, Acad Integrat Med, Fuzhou 350122, Fujian, Peoples R China
[2] Fujian Univ Tradit Chinese Med, Fujian Key Lab Integrat Med Geriatr, Fuzhou 350122, Fujian, Peoples R China
关键词
chloroform fraction of Scutellaria barbata D. Don; colorectal cancer; apoptosis; proliferation; miR-34a; Notch1/2; Jagged1; Bcl-2; CARCINOMA CELLS; DOWN-REGULATION; APOPTOSIS; PATHWAY; MICRORNAS; SUPPRESSION; MODULATION; BCL-2; NOTCH; STATISTICS;
D O I
10.3892/or.2017.5625
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Scutellaria barbata D. Don (SB) is a well known formula in traditional Chinese medicine, which exhibits potent anticancer effects on various cancers. Many miRNAs play crucial roles in the regulation of cancer, for instance, miR-34a functions as a tumor suppressor, and is often downregulated during cancer. In this study, we investigated the role of ECSB in suppressing the growth of human colon cancer HCT-8 cells, and whether this is mediated by regulation of miR-34a and its downstream target genes, using real-time PCR and western blot analysis. ECSB treatment significantly inhibited the proliferation of HCT-8 cells and promoted apoptosis in a dose dependent manner. In addition, ECSB treatment significantly increased the level of miR-34a expression and decreased the levels of Bcl-2, Notchl/2 and Jagged1 expression. Furthermore, knockdown of miR-34a expression through transfection of anti-miR-34a oligonucleotide was significantly reversed by ECSB treatment. Likewise, knockdown of miR-34a resulted in significant upregulation of Bcl-2, Notchl/2 and Jagged1 expression, which was reversed following ECSB treatment. Therefore, this study reveals that ECSB inhibited cancer cell growth via promoting apoptosis and inhibiting proliferation, through regulation of miR-34a. These findings further support the use of ECSB as an effective therapeutic agent against colon cancer.
引用
收藏
页码:3695 / 3701
页数:7
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