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Using Small Molecules to Dissect Non-apoptotic Programmed Cell Death: Necroptosis, Ferroptosis, and Pyroptosis

期刊

CHEMBIOCHEM
卷 16, 期 18, 页码 2557-2561

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201500422

关键词

cancer; ferroptosis; necroptosis; programmed cell death; pyroptosis; signal transduction

资金

  1. National High Technology Project 973 [2012CB837400, 2015CB856200]
  2. NNSFC [21222209, 21472010, 91313303]

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Genetically programmed cell death is a universal and fundamental cellular process in multicellular organisms. Apoptosis and necroptosis, two common forms of programmed cell death, play vital roles in maintenance of homeostasis in metazoans. Dysfunction of the regulatory machinery of these processes can lead to carcinogenesis or autoimmune diseases. Inappropriate death of essential cells can lead to organ dysfunction or even death; ischemia-reperfusion injury and neuro-degenerative disorders are examples of this. Recently, novel forms of non-apoptotic programmed cell death have been identified. Although these forms of cell death play significant roles in both physiological and pathological conditions, the detailed molecular mechanisms underlying them are still poorly understood. Here, we discuss progress in using small molecules to dissect three forms of non-apoptotic programmed cell death: necroptosis, ferroptosis, and pyroptosis.

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