Yuan Zhu-Hui, Liu Tong, Wang Hao, Xue Li-Xiang, Wang Jun-Jie
Department of Radiation Oncology, Peking University Third Hospital, Beijing, China.
Center of Basic Medical Research, Institute of Medical Innovation and Research, Peking University Third Hospital, Beijing, China.
Front Cell Dev Biol. 2021 Jun 24;9:675617. doi: 10.3389/fcell.2021.675617. eCollection 2021.
Exposure of tumor cells to ionizing radiation (IR) alters the microenvironment, particularly the fatty acid (FA) profile and activity. Moreover, abnormal FA metabolism, either catabolism or anabolism, is essential for synthesizing biological membranes and delivering molecular signals to induce ferroptotic cell death. The current review focuses on the bistable regulation characteristics of FA metabolism and explains how FA catabolism and anabolism pathway crosstalk harmonize different ionizing radiation-regulated ferroptosis responses, resulting in pivotal cell fate decisions. In summary, targeting key molecules involved in lipid metabolism and ferroptosis may amplify the tumor response to IR.
肿瘤细胞暴露于电离辐射(IR)会改变微环境,尤其是脂肪酸(FA)谱和活性。此外,异常的FA代谢,无论是分解代谢还是合成代谢,对于合成生物膜和传递分子信号以诱导铁死亡细胞死亡至关重要。本综述聚焦于FA代谢的双稳态调节特征,并解释FA分解代谢和合成代谢途径的相互作用如何协调不同的电离辐射调节的铁死亡反应,从而导致关键的细胞命运决定。总之,靶向参与脂质代谢和铁死亡的关键分子可能会增强肿瘤对IR的反应。