Literature DB >> 24907642

Novel nuclear localization of fatty acid synthase correlates with prostate cancer aggressiveness.

Allison A Madigan1, Kevin J Rycyna1, Anil V Parwani2, Yeipyeng J Datiri3, Ahmed M Basudan1, Kathryn M Sobek1, Jessica L Cummings1, Per H Basse4, Dean J Bacich5, Denise S O'Keefe6.   

Abstract

Fatty acid synthase is up-regulated in a variety of cancers, including prostate cancer. Up-regulation of fatty acid synthase not only increases production of fatty acids in tumors but also contributes to the transformed phenotype by conferring growth and survival advantages. In addition, increased fatty acid synthase expression in prostate cancer correlates with poor prognosis, although the mechanism(s) by which this occurs are not completely understood. Because fatty acid synthase is expressed at low levels in normal cells, it is currently a major target for anticancer drug design. Fatty acid synthase is normally found in the cytosol; however, we have discovered that it also localizes to the nucleus in a subset of prostate cancer cells. Analysis of the fatty acid synthase protein sequence indicated the presence of a nuclear localization signal, and subcellular fractionation of LNCaP prostate cancer cells, as well as immunofluorescent confocal microscopy of patient prostate tumor tissue and LNCaPs confirmed nuclear localization of this protein. Finally, immunohistochemical analysis of prostate cancer tissue indicated that nuclear localization of fatty acid synthase correlates with Gleason grade, implicating a potentially novel role in prostate cancer progression. Possible clinical implications include improving the accuracy of prostate biopsies in the diagnosis of low- versus intermediate-risk prostate cancer and the uncovering of novel metabolic pathways for the therapeutic targeting of androgen-independent prostate cancer.
Copyright © 2014 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 24907642      PMCID: PMC4116692          DOI: 10.1016/j.ajpath.2014.04.012

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  25 in total

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