机构:
Columbia Univ, Dept Chem, New York, NY 10027 USA
Columbia Univ, Dept Biol Sci, New York, NY 10027 USAColumbia Univ, Dept Chem, New York, NY 10027 USA
Stockwell, Brent R.
[1
,2
]
Jiang, Xuejun
论文数: 0引用数: 0
h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, New York, NY 10065 USAColumbia Univ, Dept Chem, New York, NY 10027 USA
Jiang, Xuejun
[3
]
机构:
[1] Columbia Univ, Dept Chem, New York, NY 10027 USA
[2] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10065 USA
Ferroptosis is a recently described form of cell death driven by iron-dependent lipid peroxidation. This type of cell death was first observed in response to treatment of tumor cells with a small-molecule chemical probe named erastin. Most subsequent advances in understanding the mechanisms governing ferroptosis involved the use of genetic screens and small-molecule probes. We describe herein the utility and limitations of chemical probes that have been used to analyze and perturb ferroptosis, as well as mechanistic studies of ferroptosis that benefit Led from the use of these probes and genetic screens. We also suggest probes for ferroptosis and highlight mechanistic questions surrounding this form of cell death that will be a high priority for exploration in the future.