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Gypenosides Synergistically Enhances the Anti-Tumor Effect of 5-Fluorouracil on Colorectal Cancer In Vitro and In Vivo: A Role for Oxidative Stress-Mediated DNA Damage and p53 Activation

机译:绞股蓝总皂甙协同增强5-氟尿嘧啶体外和体内抗肿瘤作用:氧化应激介导的DNA损伤和p53激活的作用。

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摘要

Objective5-Fluorouracil (5-Fu) has been widely used as a first-line drug for colorectal cancer (CRC) treatment but limited by drug resistance and severe toxicity. The chemo-sensitizers that augment its efficiency and overcome its limitation are urgently needed. Gypenosides (Gyp), the main components from Gynostemma pentaphyllum (Thunb.) Makino, has shown potential anti-tumor property with little side-effect. Here, we carefully explored the chemo-sensitization of Gyp to potentiate the anti-tumor effect of 5-Fu in vitro and in vivo.
机译:Objective5-氟尿嘧啶(5-Fu)已被广泛用作结直肠癌(CRC)治疗的一线药物,但受耐药性和严重毒性的限制。迫切需要提高其效率并克服其局限性的化学增敏剂。绞股蓝绞股蓝(Gynostemma pentaphyllum(Thunb。)Makino)的主要成分绞股蓝总皂甙(Gyp)具有潜在的抗肿瘤特性,几乎没有副作用。在这里,我们仔细研究了Gyp的化学增敏作用,以增强5-Fu在体外和体内的抗肿瘤作用。

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