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摘要:
Radiotherapy is commonly used to treat advanced pancreatic cancers and can improve survival by 2 months in combination with gemcitabine. However, prognosis and survival improvement remain unsatisfactory, and effective therapies are urgently needed. Piperlongumine has been demonstrated to have therapeutic potentials against various cancers. In this study, we synthesized a series of piperlongumine derivatives and provided evidence that piperlongumine derivatives could be used as effective radiosensitizers in pancreatic cancer. Two compounds enhanced the radiosensitivity of Panc-1 and SW1990 cells. In a pancreatic bi-flank xenograft tumor model, they significantly inhibited tumor growth. Piperlongumine derivatives could induce reactive oxygen species (ROS) expression and regulate the Keap1-Nrf2 protective pathway with enhancement of radiation-induced DNA damage, G2/M-phase cell cycle arrest, and apoptosis. Collectively, our data offer a proof of concept for the use of piperlongumine derivatives as a novel class of radiosensitizers for the treatment of pancreatic cancer.
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篇名 Radiosensitization of human pancreatic cancer by piperlongumine analogues
来源期刊 中国化学快报(英文版) 学科
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年,卷(期) 2021,(3) 所属期刊栏目 Communications
研究方向 页码范围 1197-1201
页数 5页 分类号
字数 语种 英文
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中国化学快报(英文版)
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1001-8417
11-2710/O6
16开
北京市先农坛街1号
1990
eng
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