顺铂
PI3K/AKT/mTOR通路
化学
细胞凋亡
体内
联合疗法
药理学
癌症
癌细胞
转移
蛋白激酶B
宫颈癌
热休克蛋白90
癌症研究
细胞周期检查点
细胞周期
化疗
医学
内科学
生物化学
生物
生物技术
热休克蛋白
基因
作者
Jinsen Liang,Dandan Wang,Yijin Zhao,Yihe Wu,Xuelian Liu,Lilan Xin,Junhong Dai,Hang Ren,Hai‐Bing Zhou,Hongbing Cai,Chune Dong
标识
DOI:10.1016/j.ejmech.2024.116572
摘要
The development of effective drugs for cervical cancer is urgently required because of its high mortality rate and the limited treatment options. Herein, we report the design, synthesis, and evaluation of a series of novel and effective Hsp90-targeting PROTACs. These compounds exhibited potent anti-proliferative activity against cervical cancer cells with low IC50 values. Compound lw13 effectively degraded Hsp90 at a concentration of only 0.05 μM. In addition, it can inhibit the metastasis of cancer cells and induce significant cell cycle arrest and apoptosis. Furthermore, lw13 demonstrated remarkable antitumor activity both in vitro and in vivo, and has a synergistic effect in combination with cisplatin. Moreover, lw13 can prevent the activation of the HER2/AKT/mTOR signaling pathway by indirectly reducing the levels of HER2 and AKT. This study paves the way for cancer treatment and provides valuable insights into the combination therapy of cervical cancer.
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