Impaired mitochondrial metabolism and mammary carcinogenesis.

TitleImpaired mitochondrial metabolism and mammary carcinogenesis.
Publication TypeJournal Article
Year of Publication2013
AuthorsYadava N, Schneider SS, Jerry JD, Kim C
JournalJ Mammary Gland Biol Neoplasia
Volume18
Issue1
Pagination75-87
Date Published2013 Mar
ISSN1573-7039
KeywordsAnimals, Breast Neoplasms, Carcinogens, Environmental, Disease Susceptibility, Environmental Exposure, Female, Humans, Mammary Glands, Animal, Mammary Glands, Human, Mitochondria, Oxidative Phosphorylation
Abstract

Mitochondrial oxidative metabolism plays a key role in meeting energetic demands of cells by oxidative phosphorylation (OxPhos). Here, we have briefly discussed (a) the dynamic relationship that exists among glycolysis, the tricarboxylic acid (TCA) cycle, and OxPhos; (b) the evidence of impaired OxPhos (i.e. mitochondrial dysfunction) in breast cancer; (c) the mechanisms by which mitochondrial dysfunction can predispose to cancer; and (d) the effects of host and environmental factors that can negatively affect mitochondrial function. We propose that impaired OxPhos could increase susceptibility to breast cancer via suppression of the p53 pathway, which plays a critical role in preventing tumorigenesis. OxPhos is sensitive to a large number of factors intrinsic to the host (e.g. inflammation) as well as environmental exposures (e.g. pesticides, herbicides and other compounds). Polymorphisms in over 143 genes can also influence the OxPhos system. Therefore, declining mitochondrial oxidative metabolism with age due to host and environmental exposures could be a common mechanism predisposing to cancer.

DOI10.1007/s10911-012-9271-3
Alternate JournalJ Mammary Gland Biol Neoplasia
PubMed ID23269521