HDAC3 overexpression and colon cancer cell proliferation and differentiation

Authors

  • Colleen C. Spurling,

    1. Department of Molecular & Cell Biology, University of Connecticut, Storrs, Connecticut
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  • Cassandra A. Godman,

    1. Department of Molecular & Cell Biology, University of Connecticut, Storrs, Connecticut
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  • Emily J. Noonan,

    1. Department of Molecular & Cell Biology, University of Connecticut, Storrs, Connecticut
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  • Theodore P. Rasmussen,

    1. Department of Molecular & Cell Biology, University of Connecticut, Storrs, Connecticut
    2. Center for Regenerative Biology, University of Connecticut, Storrs, Connecticut
    3. Department of Animal Science, University of Connecticut, Storrs, Connecticut
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  • Daniel W. Rosenberg,

    1. Center for Molecular Medicine, University of Connecticut Health Center, Farmington, Connecticut
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  • Charles Giardina

    Corresponding author
    1. Department of Molecular & Cell Biology, University of Connecticut, Storrs, Connecticut
    • Department of Molecular & Cell Biology, 91 North Eagleville Road, U-3125, University of Connecticut, Storrs, CT 06269.
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  • Colleen C. Spurling and Cassandra A. Godman contributed equally to this manuscript.

Abstract

An immunohistochemical analysis of human colorectal adenocarcinomas showed that cancer cells express widely varying levels of HDAC3. The SW480 colon cancer cell line was found to express high levels of HDAC3 compared to other colon cancer cell lines. p21 was poorly induced in SW480 cells relative to the lower HDAC3-expressing HT-29 cells. RNAi-induced reduction of HDAC3 in SW480 cells increased their constitutive, butyrate-, TSA-, and TNF-α-induced expression of p21, but did not cause all the gene expression changes induced upon general histone deacetylase (HDAC) inhibition. SW480 cells with lower HDAC3 expression appeared to be poised for gene expression responses with increased histone H4-K12 acetylation, but not K5, K8, or K16 acetylation. Even though p21 was readily activated in HT29 cells, HDAC3 siRNA nonetheless stimulated p21 expression in these cells to a greater degree than HDAC1 and HDAC2 siRNA. SW480 cells with lower HDAC3 levels displayed an enhanced cell cycle arrest and growth inhibition by butyrate, but without changes in apoptosis or sensitivity to chemotherapeutic agents. As reported for other colon cancer cell lines, butyrate induced the rapid downregulation of the secretory cell differentiation markers mucin 2 and intestinal trefoil factor in SW480 cells. Interestingly, selective HDAC3 inhibition was sufficient to downregulate these genes. Our data support a central role for HDAC3 in regulating the cell proliferation and differentiation of colon cancer cells and suggest a potential mechanism by which colon cancers may become resistant to luminal butyrate. © 2007 Wiley-Liss, Inc.

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