Mohammadi Ali, Mansoori Behzad, Baradaran Pooneh Chokhachi, Baradaran Sepideh Chokhachi, Baradaran Behzad
Immunology Research Center, Tabriz University of Medical Sciences, daneshghah Ave, Tabriz, Iran.
Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
J Gastrointest Cancer. 2017 Dec;48(4):333-340. doi: 10.1007/s12029-016-9884-7.
Colorectal cancer is the second leading cause of cancer mortality in the USA. There are a number of medicinal plants triggering apoptosis response in cancer cells, thus have a therapeutic potential. On the other hand, due to traditional uses and availability of Anacyclus pyrethrum extract, we decided to evaluate the efficacy of this medicinal herb on human colorectal cancer cell line (HCT).
In the present study, the cytotoxic effects of Anacyclus pyrethrum extract were assessed by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay, and trypan blue viability dye. Then, flow cytometry assay was exploited to measure cell death and apoptosis stage. The scratch test was exploited to assess the effect of Anacyclus pyrethrum on the migration of cancer cells. The expression levels of Caspase 3, Bcl-2, MMP1, and Vimentin genes were quantified by real-time PCR. Finally, cell cycle was analyzed by flow cytometry.
MTT assay showed that Anacyclus pyrethrum extract significantly inhibited the cell growth. According to the flow cytometry assay result, the herbal extract was able to induce apoptosis in colorectal cancer cells. Our findings also demonstrated that the plant extract substantially increases the caspase 3 mRNA expression, while decreases Bcl-2, MMP1, and Vimentin. Cell cycle arrest occurred in G1 stage, due to the results of flow cytometry.
These results indicate that Anacyclus pyrethrum extract can successfully induce apoptosis in HCT cells. Therefore, it could be used as a novel therapeutic candidate for colorectal cancer treatment.
结直肠癌是美国癌症死亡的第二大主要原因。有许多药用植物可引发癌细胞的凋亡反应,因此具有治疗潜力。另一方面,鉴于刺籽番荔枝提取物的传统用途和可得性,我们决定评估这种草药对人结肠癌细胞系(HCT)的疗效。
在本研究中,通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)法和台盼蓝活力染料评估刺籽番荔枝提取物的细胞毒性作用。然后,利用流式细胞术检测细胞死亡和凋亡阶段。利用划痕试验评估刺籽番荔枝对癌细胞迁移的影响。通过实时PCR定量分析半胱天冬酶3、Bcl-2、基质金属蛋白酶1和波形蛋白基因的表达水平。最后,通过流式细胞术分析细胞周期。
MTT试验表明,刺籽番荔枝提取物显著抑制细胞生长。根据流式细胞术检测结果,该草药提取物能够诱导结肠癌细胞凋亡。我们的研究结果还表明,该植物提取物可显著增加半胱天冬酶3 mRNA的表达,同时降低Bcl-2、基质金属蛋白酶1和波形蛋白的表达。流式细胞术结果显示,细胞周期停滞在G1期。
这些结果表明,刺籽番荔枝提取物可成功诱导HCT细胞凋亡。因此,它可作为一种新型的结直肠癌治疗候选药物。