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关于铁死亡的稳健且可重复研究的建议。

Recommendations for robust and reproducible research on ferroptosis.

作者信息

Mishima Eikan, Nakamura Toshitaka, Doll Sebastian, Proneth Bettina, Fedorova Maria, Pratt Derek A, Friedmann Angeli José Pedro, Dixon Scott J, Wahida Adam, Conrad Marcus

机构信息

Institute of Metabolism and Cell Death, Molecular Targets and Therapeutics Center, Helmholtz Munich, Neuherberg, Germany.

Department of Nephrology, Tohoku University Graduate School of Medicine, Sendai, Japan.

出版信息

Nat Rev Mol Cell Biol. 2025 Apr 9. doi: 10.1038/s41580-025-00843-2.

Abstract

Ferroptosis is a necrotic, non-apoptotic cell death modality triggered by unrestrained iron-dependent lipid peroxidation. By unveiling the regulatory mechanisms of ferroptosis and its relevance to various diseases, research over the past decade has positioned ferroptosis as a promising therapeutic target. The rapid growth of this research field presents challenges, associated with potentially inadequate experimental approaches that may lead to misinterpretations in the assessment of ferroptosis. Typical examples include assessing whether an observed phenotype is indeed linked to ferroptosis, and selecting appropriate animal models and small-molecule modulators of ferroptotic cell death. This Expert Recommendation outlines state-of-the-art methods and tools to reliably study ferroptosis and increase the reproducibility and robustness of experimental results. We present highly validated compounds and animal models, and discuss their advantages and limitations. Furthermore, we provide an overview of the regulatory mechanisms and the best-studied players in ferroptosis regulation, such as GPX4, FSP1, SLC7A11 and ACSL4, discussing frequent pitfalls in experimental design and relevant guidance. These recommendations are intended for researchers at all levels, including those entering the expanding and exciting field of ferroptosis research.

摘要

铁死亡是一种由不受控制的铁依赖性脂质过氧化引发的坏死性、非凋亡性细胞死亡方式。通过揭示铁死亡的调控机制及其与各种疾病的相关性,过去十年的研究已将铁死亡定位为一个有前景的治疗靶点。这一研究领域的快速发展带来了挑战,这些挑战与可能导致在铁死亡评估中出现误解的潜在不充分实验方法有关。典型的例子包括评估观察到的表型是否确实与铁死亡相关,以及选择合适的动物模型和铁死亡细胞死亡的小分子调节剂。本专家建议概述了可靠研究铁死亡并提高实验结果的可重复性和稳健性的最新方法和工具。我们展示了经过高度验证的化合物和动物模型,并讨论了它们的优缺点。此外,我们概述了铁死亡调控的机制以及铁死亡调控中研究最多的参与者,如谷胱甘肽过氧化物酶4(GPX4)、铁死亡抑制蛋白1(FSP1)、溶质载体家族7成员11(SLC7A11)和长链脂酰辅酶A合成酶4(ACSL4),讨论了实验设计中常见的陷阱及相关指导。这些建议适用于各级研究人员,包括那些进入不断扩展且令人兴奋的铁死亡研究领域的人员。

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