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首页> 外文期刊>Molecular Carcinogenesis >Metabolite of ellagitannins, urolithin A induces autophagy and inhibits metastasis in human sw620 colorectal cancer cells
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Metabolite of ellagitannins, urolithin A induces autophagy and inhibits metastasis in human sw620 colorectal cancer cells

机译:脲腈蛋白的代谢物,Urokithin A诱导自噬并抑制人SW620结直肠癌细胞中的转移

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摘要

Autophagy is an evolutionarily conserved pathway in which cytoplasmic contents are degraded and recycled. This study found that submicromolar concentrations of urolithin A, a major polyphenol metabolite, induced autophagy in SW620 colorectal cancer (CRC) cells. Exposure to urolithin A also dose-dependently decreased cell proliferation, delayed cell migration, and decreased matrix metalloproteinas-9 (MMP-9) activity. In addition, inhibition of autophagy by Atg5-siRNA, caspases by Z-VAD-FMK suppressed urolithin A-stimulated cell death and anti-metastatic effects. Micromolar urolithin A concentrations induced both autophagy and apoptosis. Urolithin A suppressed cell cycle progression and inhibited DNA synthesis. These results suggest that dietary consumption of urolithin A could induce autophagy and inhibit human CRC cell metastasis. Urolithins may thus contribute to CRC treatment and offer an alternative or adjunct chemotherapeutic agent to combat this disease.
机译:自噬是一种进化的保守途径,其中细胞质内容物降解并再循环。 本研究发现,尿嘧啶A的亚微粒浓度A,主要的多酚代谢物,在SW620结肠直肠癌(CRC)细胞中诱导的自噬。 暴露于尿道素A也剂量依赖性降低细胞增殖,延迟细胞迁移和降低的基质金属蛋白酶-9(MMP-9)活性。 此外,通过ATG5-siRNA,Caspases通过Z-VAD-FMK抑制自噬抑制尿嘧啶A刺激的细胞死亡和抗转移效果。 MicroMolar Urokithin浓度诱导自噬和凋亡。 尿道素抑制细胞周期进展并抑制DNA合成。 这些结果表明尿素素A的膳食消费可以诱导自噬并抑制人类CRC细胞转移。 因此,尿道素可能导致CRC治疗,并提供替代或兼容化学治疗剂以对抗这种疾病。

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