Nakajima Kazuma, Nishizawa Hironari, Chen Guan, Tsuge Shunichi, Yamanaka Mie, Kiyohara Machi, Irikura Riko, Matsumoto Mitsuyo, Tanaka Kozo, Narikawa Rei, Igarashi Kazuhiko
Department of Biochemistry, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan.
Department of Molecular Oncology, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan.
J Biochem. 2024 Dec 2;176(6):472-483. doi: 10.1093/jb/mvae067.
Ferroptosis is a cell death mechanism mediated by iron-dependent lipid peroxidation. Although ferroptosis has garnered attention as a cancer-suppressing mechanism, there are still limited markers available for identifying ferroptotic cells or assessing their sensitivity to ferroptosis. The study focused on biliverdin, an endogenous reducing substance in cells, and examined the dynamics of intracellular biliverdin during ferroptosis using a biliverdin-binding cyanobacteriochrome. It was found that intracellular biliverdin decreases during ferroptosis and that this decrease is specific to ferroptosis amongst different forms of cell death. Furthermore, the feasibility of predicting sensitivity to ferroptosis by measuring intracellular biliverdin was demonstrated using a ferroptosis model induced by the re-expression of the transcription factor BACH1. These findings provide further insight into ferroptosis research and are expected to contribute to the development of cancer therapies that exploit ferroptosis.
铁死亡是一种由铁依赖性脂质过氧化介导的细胞死亡机制。尽管铁死亡作为一种癌症抑制机制已受到关注,但用于识别铁死亡细胞或评估其对铁死亡敏感性的标志物仍然有限。该研究聚焦于细胞内的内源性还原物质胆红素,并使用胆红素结合蓝细菌视蛋白研究了铁死亡过程中细胞内胆红素的动态变化。研究发现,在铁死亡过程中细胞内胆红素减少,且这种减少在不同形式的细胞死亡中对铁死亡具有特异性。此外,使用转录因子BACH1重新表达诱导的铁死亡模型证明了通过测量细胞内胆红素来预测对铁死亡敏感性的可行性。这些发现为铁死亡研究提供了进一步的见解,并有望为开发利用铁死亡的癌症治疗方法做出贡献。