Demir Selim, Turan Ibrahim, Aliyazicioglu Yuksel, Kilinc Kagan, Yaman Serap Ozer, Ayazoglu Demir Elif, Arslan Ayse, Mentese Ahmet, Deger Orhan
a Department of Nutrition and Dietetics , Faculty of Health Sciences, Karadeniz Technical University , Trabzon , Turkey.
b Department of Genetic and Bioengineering , Faculty of Engineering and Natural Sciences, Gumushane University , Gumushane , Turkey.
Nutr Cancer. 2017 Jan;69(1):74-83. doi: 10.1080/01635581.2017.1247887. Epub 2016 Nov 23.
Many studies have reported cytotoxic effects of different Morus species, but there have been only limited studies on the cytotoxic effect of Morus rubra. The aims of this study were to evaluate the cytotoxic effect of dimethyl sulfoxide extract of M. rubra and to investigate, for the first time, its probable cytotoxic activity in human colon cancer (WiDr) cells, together with the mechanism involved. The cytotoxic activity of extract was determined using MTT assay. The mechanism involved in the cytotoxic effect of extract was then evaluated in terms of apoptosis, and the cell cycle using flow cytometry, mitochondrial membrane potential (MMP) was investigated using the fluorometric method, and expression levels of telomerase and C/EBP homologous protein (CHOP) were investigated using reverse-transcription PCR (RT-PCR). M. rubra extract exhibited moderate selective cytotoxicity on colon cancer cells compared with fibroblast cells. Extract induced cell cycle arrest at the G phase and apoptosis via reduced MMP in WiDr cells. Additionally, M. rubra extract significantly repressed telomerase and induced CHOP expressions in WiDr cells. Our results demonstrate that targeting telomerase and endoplasmic reticulum stress represents a promising strategy in colon cancer therapy, and M. rubra may have considerable potential for development as a novel natural product-based anticancer agent.
许多研究报告了不同桑属植物的细胞毒性作用,但关于红桑细胞毒性作用的研究却很有限。本研究的目的是评估红桑二甲基亚砜提取物的细胞毒性作用,并首次研究其在人结肠癌(WiDr)细胞中的潜在细胞毒性活性及其相关机制。采用MTT法测定提取物的细胞毒性活性。然后从细胞凋亡、细胞周期方面,利用流式细胞术评估提取物细胞毒性作用的机制,采用荧光法研究线粒体膜电位(MMP),并利用逆转录聚合酶链反应(RT-PCR)研究端粒酶和C/EBP同源蛋白(CHOP)的表达水平。与成纤维细胞相比,红桑提取物对结肠癌细胞表现出适度的选择性细胞毒性。提取物通过降低WiDr细胞的MMP诱导细胞周期阻滞在G期并诱导细胞凋亡。此外,红桑提取物显著抑制WiDr细胞中的端粒酶并诱导CHOP表达。我们的结果表明,靶向端粒酶和内质网应激是结肠癌治疗中一种有前景的策略,红桑作为一种新型的基于天然产物的抗癌剂可能具有相当大的开发潜力。