自噬
多糖
毒性
药理学
体内
氧化应激
化疗
化学
免疫系统
炎症
医学
生物
免疫学
生物化学
生物技术
内科学
细胞凋亡
有机化学
作者
Hao Chen,Zhuang Wang,Lei Gong,Jielin Chen,Yuzhe Huang,Wenqiang Guo,Qian Zhang,Yong Li,Guan‐Hu Bao,Daxiang Li,Yan Chen
标识
DOI:10.1016/j.ijbiomac.2024.130697
摘要
Chemotherapy, the most common class of anticancer drugs, is considerably limited owing to its adverse side effects. In this study, we aimed to evaluate the protective effect and mechanism of action of large-leaf yellow tea polysaccharides (ULYTP-1, 1.29 × 104 Da) against chemotherapeutic 5-fluorouracil (5-Fu). Structural characterisation revealed that ULYTP-1 was a β-galactopyranouronic acid. Furthermore, ULYTP-1 promoted autolysosome formation, activating autophagy and reducing the oxidative stress and inflammation caused by 5-Fu. Our in vivo study of 4 T1 tumour-bearing mice revealed that ULYTP-1 also attenuated 5-Fu toxicity through modulation of the gut microbiota. Moreover, ULYTP-1 effectively protected immune organs and the liver from 5-Fu toxicity, while promoting its tumour-inhibitory properties. The current findings provide a new strategy for optimising chemotherapy regimens in the clinic.
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