Prostate Cancer Scientific Abstracts - G. Dakubo
Welcome to the Prostate Cancer Guide scientific abstracts, author section G. Dakubo.
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Selected Gabriel Dakubo prostate cancer abstracts
Journal: Journal of Clinical Pathology
Pubmed ID: 16394275
Authors: Dakubo GD, Parr RL, Costello LC, Franklin RB, Thayer RE.Title: Altered metabolism and mitochondrial genome in prostate
cancer.
Mutations in mitochondrial DNA are frequent in cancer and the accompanying
mitochondrial dysfunction and altered intermediary metabolism might contribute
to, or signal, tumour pathogenesis. The metabolism of human prostate peripheral
zone glandular epithelial cells is unique. Compared with many other soft
tissues, these glandular epithelial cells accumulate high concentrations of
zinc, which inhibits the activity of m-aconitase, an enzyme involved in citrate
metabolism through Krebs cycle. This causes Krebs cycle truncation and
accumulation of high concentrations of citrate to be secreted in prostatic
fluid. The accumulation of zinc also inhibits terminal oxidation. Therefore,
these cells exhibit inefficient energy production. In contrast, malignant
transformation of the prostate is associated with an early metabolic switch,
leading to decreased zinc accumulation and increased citrate oxidation. The
efficient energy production in these transformed cells implies increased
electron transport chain activity, increased oxygen consumption, and perhaps,
excess reactive oxygen species (ROS) production compared with normal prostate
epithelial cells. Because ROS have deleterious effects on DNA, proteins, and
lipids, the altered intermediary metabolism may be linked with ROS production
and accelerated mitochondrial DNA mutations in prostate cancer.
Contact: Genesis Genomics Inc, 1294 Balmoral Street, Thunder Bay, Ontario, Canada, P7B 5Z5.
gabriel.dakubo@genesisgenomics.com.