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  • Powerhouse down: Complex II dissociation in the respiratory chain

    Author(s)
    Hwang, Ming-Shih
    Rohlena, Jakub
    Dong, Lan-Feng
    Neuzil, Jiri
    Grimm, Stefan
    Griffith University Author(s)
    Neuzil, Jiri
    Year published
    2014
    Metadata
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    Abstract
    Complex II of the respiratory chain (RC) recently emerged as a prominent regulator of cell death. In both cancer cells as well as neurodegenerative diseases, mutations in subunits have been found along with other genetic alterations indirectly affecting this complex. Anticancer compounds were developed that target complex II and cause cell death in a tumor-specific way. Our mechanistic understanding of how complex II is activated for cell death induction has recently been made clearer in recent studies, the results of which are covered in this review. This protein assembly is specifically activated for cell death via the ...
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    Complex II of the respiratory chain (RC) recently emerged as a prominent regulator of cell death. In both cancer cells as well as neurodegenerative diseases, mutations in subunits have been found along with other genetic alterations indirectly affecting this complex. Anticancer compounds were developed that target complex II and cause cell death in a tumor-specific way. Our mechanistic understanding of how complex II is activated for cell death induction has recently been made clearer in recent studies, the results of which are covered in this review. This protein assembly is specifically activated for cell death via the dissociation of its SDHA and SDHB subunits from the membrane-anchoring proteins through pH change or mitochondrial Ca2 + influx. The SDH activity contained in the SDHA/SDHB subcomplex remains intact and then generates, in an uncontrolled fashion, excessive amounts of reactive oxygen species (ROS) for cell death. Future studies on this mitochondrial complex will further elucidate it as a target for cancer treatments and reveal its role as a nexus for many diverse stimuli in cell death signaling.
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    Journal Title
    Mitochondrion
    Volume
    19
    DOI
    https://doi.org/10.1016/j.mito.2014.06.001
    Subject
    Genetics
    Cancer cell biology
    Publication URI
    http://hdl.handle.net/10072/67207
    Collection
    • Journal articles

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