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Title: INOSITOL HEXAKISPHOSPHATE MEDIATES APOPTOSIS IN HUMAN BREAST ADENOCARCINOMA MCF-7 CELL LINE VIA INTRINSIC PATHWAY

Journal Article · · AIP Conference Proceedings
DOI:https://doi.org/10.1063/1.3419682· OSTI ID:21367153
 [1];  [2]
  1. Department of Toxicology and Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, Arkansas (United States)
  2. Graduate Institute of Technology, University of Arkansas at Little Rock, Little Rock, Arkansas (United States)

Inositol polyphosphates (InsP{sub s}) are naturally occurring compounds ubiquitously present in plants and animals. Inositol hexakisphosphate (InsP{sub 6}) is the most abundant among all InsP{sub s} and constitutes the major portion of dietary fiber in most cereals, legumes and nuts. Certain derivatives of InsP{sub s} also regulate cellular signaling mechanisms. InsP{sub s} have also been shown to reduce tumor formation and induce apoptosis in cancerous cells. Therefore, in this study, the effects of InsPs on apoptosis were studied in an attempt to investigate their potential anti-cancer therapeutic application and understand their mechanism of action. Acridine orange and ethidium bromide staining suggested that InsP{sub 6} dose dependently induced apoptosis in human breast adenocarcinoma MCF-7 cells. Among InsP{sub s} tested (InsP{sub 3}, InsP{sub 4}, InsP{sub 5}, and InsP{sub 6}), InsP{sub 6} was found to be the most effective in inducing apoptosis. Furthermore, effects of InsP{sub 6} were found most potent inducing apoptosis. Etoposide, the drug known to induce apoptosis in both in vivo and in vitro, was used as a positive control. Western blotting experiments using specific antibodies against known apoptotic markers suggested that InsP{sub 6} induced apoptotic changes were mediated via an intrinsic apoptotic pathway.

OSTI ID:
21367153
Journal Information:
AIP Conference Proceedings, Vol. 1229, Issue 1; Conference: 4. BioNanoTox (Biology, Nanotechnology, Toxicology) and applications research conference, Little Rock, AK (United States), 21-22 Oct 2009; Other Information: DOI: 10.1063/1.3419682; (c) 2010 American Institute of Physics; ISSN 0094-243X
Country of Publication:
United States
Language:
English