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橄榄苦苷通过依赖 p53 的途径发挥对结直肠癌的抗癌活性。

Helveticoside Exhibited p53-dependent Anticancer Activity Against Colorectal Cancer.

机构信息

College of Pharmacy, Henan University of Chinese Medicine, Zhengzhou, Henan, China.

Basic Medicine College, Henan University of Chinese Medicine, Zhengzhou, Henan, China.

出版信息

Arch Med Res. 2020 Apr;51(3):224-232. doi: 10.1016/j.arcmed.2020.02.007. Epub 2020 Mar 6.

Abstract

BACKGROUND

Investigation into the anti-cancer activities of natural products and their derivatives represents an efficient approach to develop safe and effective chemotherapeutic agents for the treatment of colorectal cancer. Helveticoside is a biologically active component of the seed extract of Descurainia sophia. This compound has been reported to regulate the genes related to cell proliferation and apoptosis in lung cancer cells, however its anticancer activity has not been fully explored yet.

METHODS

Cell viability was evaluated by MTT and Trypan blue exclusion assay; cell apoptosis was measured by flow cytometry; mitochondrial membrane potential was determined by using JC1-mitochondrial membrane potential assay kit; protein levels were determined by western blot assay; in vivo tumor growth was assessed in a xenograft nude mice model.

RESULTS

The current study demonstrated the in vitro anti-cancer activity of helveticoside against colorectal cancer using colorectal cancer cells SW480 and HCT116. Moreover, induction of apoptosis was found to mediate the cytotoxic action of helveticoside on SW480 and HCT116 cells. Based on the decrease in the mitochondrial membrane potential, upregulation of Bax, downregulation of Bcl-2 and cleavage of caspase-3 and 9, apoptosis was induced by helveticoside via mitochondria-mediated intrinsic apoptotic signaling pathways in colorectal cancer cells. Besides, using p53-knockout SW480 cells, the cytotoxic action of helveticoside was found to be p53-dependent. More importantly, administration of helveticoside inhibited the growth of HCT116 cells derived-colorectal cancer xenograft in mice via activation of apoptosis.

CONCLUSIONS

Helveticoside might be a potential candidate for the development of novel chemotherapeutic agents for the treatment of colorectal cancer, while the potential toxic effects of helveticoside may be worthy of further investigations.

摘要

背景

研究天然产物及其衍生物的抗癌活性是开发安全有效的结直肠癌化疗药物的有效方法。瑞香苷是播娘蒿种子提取物中的一种生物活性成分。据报道,该化合物可调节肺癌细胞中与细胞增殖和细胞凋亡相关的基因,但尚未充分研究其抗癌活性。

方法

通过 MTT 和台盼蓝排斥试验评估细胞活力;通过流式细胞术测量细胞凋亡;通过 JC1-线粒体膜电位测定试剂盒测定线粒体膜电位;通过 Western blot 测定蛋白水平;在异种移植裸鼠模型中评估体内肿瘤生长。

结果

本研究使用结直肠癌细胞 SW480 和 HCT116 证明了 helveticoside 在体外对结直肠癌的抗癌活性。此外,发现细胞凋亡诱导介导了 helveticoside 对 SW480 和 HCT116 细胞的细胞毒性作用。基于线粒体膜电位的降低、Bax 的上调、Bcl-2 的下调以及 caspase-3 和 9 的切割,helveticoside 通过线粒体介导的内在凋亡信号通路诱导结直肠癌细胞凋亡。此外,使用 p53 敲除 SW480 细胞,发现 helveticoside 的细胞毒性作用依赖于 p53。更重要的是,helveticoside 的给药通过激活凋亡抑制了小鼠来源的 HCT116 细胞衍生的结直肠癌细胞异种移植的生长。

结论

瑞香苷可能是开发治疗结直肠癌新型化疗药物的潜在候选药物,而瑞香苷的潜在毒副作用值得进一步研究。

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