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Baicalein and baicalin inhibit colon cancer using two distinct fashions of apoptosis and senescence

机译:黄ical素和黄ical素以两种不同的凋亡和衰老方式抑制结肠癌

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摘要

Baicalein and baicalin are active components of the Scutellaria baicalensis Georgi and both have broad anti-tumor activity. However, how and whether baicalein and baicalin inhibit colon cancer is unclear. Here we demonstrate that baicalein and baicalin can significantly inhibit human colon cancer cell growth and proliferation. Furthermore, both can induce cell cycle arrest, and suppress cancer cell colony formation and migration. The suppressive effects are mechanistically due to the induction of colon cancer cell apoptosis and senescence mediated by baicalein and baicalin, respectively. Furthermore, we revealed that baicalin-induced senescence in tumor cells is due to its inhibition of telomerase reverse transcriptase expression in tumor cells, and that MAPK ERK and p38 signaling pathways are causatively involved in the regulation of colon cancer cell apoptosis and senescence mediated by baicalein and baicalin. In addition, our in vivo studies using human colon cancer cells in humanized mouse xenograft models, further demonstrated that baicalein and baicalin can induce tumor cell apoptosis and senescence, resulting in inhibition of tumorigenesis and growth of colon cancer in vivo. These data clearly suggest that baicalein and baicalin have potent anti-cancer effects against human colon cancer and could be potential novel and effective target drugs for cancer therapy.
机译:黄ical素和黄ical素是黄cut的活性成分,并且都具有广泛的抗肿瘤活性。但是,黄ical苷和黄ical苷如何以及是否抑制结肠癌尚不清楚。在这里,我们证明了黄ical素和黄ical素可以显着抑制人结肠癌细胞的生长和增殖。此外,两者均可诱导细胞周期停滞,并抑制癌细胞集落的形成和迁移。机械上的抑制作用是由于分别由黄ical苷和黄ical苷介导的结肠癌细胞凋亡和衰老的诱导。此外,我们揭示了黄ical苷诱导的肿瘤细胞衰老是由于其抑制了肿瘤细胞中端粒酶逆转录酶的表达,并且MAPK ERK和p38信号通路与黄ical苷介导的结肠癌细胞凋亡和衰老的调节有关。和黄ical苷。此外,我们在人源化小鼠异种移植模型中使用人结肠癌细胞进行的体内研究进一步证明,黄ical苷和黄ical苷可以诱导肿瘤细胞凋亡和衰老,从而在体内抑制结肠癌的发生和生长。这些数据清楚地表明黄ical苷和黄ba苷对人结肠癌具有有效的抗癌作用,并且可能是潜在的新颖有效的癌症治疗靶标药物。

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