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An inherited heteroplasmic mutation in mitochondrial gene COI in a patient with prostate cancer alters reactive oxygen, reactive nitrogen and proliferation. | LitMetric

AI Article Synopsis

  • Mitochondrial DNA (mtDNA) mutations are commonly found in various cancers, but their specific impacts on physiology are not yet fully understood.
  • In prostate cancer, both inherited and acquired mutations have been identified, particularly in the cytochrome c oxidase (COI) gene, which is crucial for mitochondrial function.
  • A rare mutation of this gene from a prostate cancer patient has been shown to reduce cytochrome oxidation while increasing levels of reactive oxygen and nitrogen, hinting at a possible role for these changes in the development of prostate cancer.

Article Abstract

Mitochondrial DNA (mtDNA) mutations have been found in many cancers but the physiological derangements caused by such mutations have remained elusive. Prostate cancer is associated with both inherited and somatic mutations in the cytochrome c oxidase (COI) gene. We present a prostate cancer patient-derived rare heteroplasmic mutation of this gene, part of mitochondrial respiratory complex IV. Functional studies indicate that this mutation leads to the simultaneous decrease in cytochrome oxidation, increase in reactive oxygen, and increased reactive nitrogen. These data suggest that mitochondrial DNA mutations resulting in increased reactive oxygen and reactive nitrogen generation may be involved in prostate cancer biology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591245PMC
http://dx.doi.org/10.1155/2013/239257DOI Listing

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