Literature DB >> 22772164

Methods for the analysis of histone H3 and H4 acetylation in blood.

Lin Rigby1, Andrea Muscat, David Ashley, Elizabeth Algar.   

Abstract

LBH589 is one of the many histone deacetylase inhibitors (HDACi) that are currently in clinical trial. Despite their wide-spread use, there is little literature available describing the typical levels of histone acetylation in untreated peripheral blood, the treatment and storage of samples to retain optimal measurement of histone acetylation nor methods by which histone acetylation analysis may be monitored and measured during the course of a patient's treatment. In this study, we have used cord or peripheral blood as a source of human leukocytes, performed a comparative analysis of sample processing methods and developed a flow cytometric method suitable for monitoring histone acetylation in isolated lymphocytes and liquid tumors. Western blotting and immunohistochemistry techniques have also been addressed. We have tested these methods on blood samples collected from four patients treated with LBH589 as part of an Australian Children's Cancer Clinical Trial (CLBH589AAU03T) and show comparable results when comparing in vitro and in vivo data. This paper does not seek to correlate histone acetylation levels in peripheral blood with clinical outcome but describes methods of analysis that will be of interest to clinicians and scientists monitoring the effects of HDACi on histone acetylation in blood samples in clinical trials or in related research studies.

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Year:  2012        PMID: 22772164      PMCID: PMC3427283          DOI: 10.4161/epi.20983

Source DB:  PubMed          Journal:  Epigenetics        ISSN: 1559-2294            Impact factor:   4.528


  25 in total

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2.  Non-random radial higher-order chromatin arrangements in nuclei of diploid human cells.

Authors:  M Cremer; J von Hase; T Volm; A Brero; G Kreth; J Walter; C Fischer; I Solovei; C Cremer; T Cremer
Journal:  Chromosome Res       Date:  2001       Impact factor: 5.239

3.  Acetylation of histone H4 plays a primary role in enhancing transcription factor binding to nucleosomal DNA in vitro.

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4.  MS-27-275, an inhibitor of histone deacetylase, has marked in vitro and in vivo antitumor activity against pediatric solid tumors.

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5.  Effect of ketoconazole-mediated CYP3A4 inhibition on clinical pharmacokinetics of panobinostat (LBH589), an orally active histone deacetylase inhibitor.

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Review 7.  Histone-deacetylase inhibitors for the treatment of cancer.

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8.  Studies on histone acetyltransferase. Partial purification and basic properties.

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Authors:  J A Croft; J M Bridger; S Boyle; P Perry; P Teague; W A Bickmore
Journal:  J Cell Biol       Date:  1999-06-14       Impact factor: 10.539

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Review 2.  Epigenetic biomarkers: Current strategies and future challenges for their use in the clinical laboratory.

Authors:  José Luis García-Giménez; Marta Seco-Cervera; Trygve O Tollefsbol; Carlos Romá-Mateo; Lorena Peiró-Chova; Pablo Lapunzina; Federico V Pallardó
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Review 4.  Developing epigenetic diagnostics and therapeutics for brain disorders.

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5.  The Depsipeptide Romidepsin Reverses HIV-1 Latency In Vivo.

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6.  Dual epigenetic targeting with panobinostat and azacitidine in acute myeloid leukemia and high-risk myelodysplastic syndrome.

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7.  Antiproliferative effects of TSA, PXD‑101 and MS‑275 in A2780 and MCF7 cells: Acetylated histone H4 and acetylated tubulin as markers for HDACi potency and selectivity.

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9.  A novel method for isolation of histones from serum and its implications in therapeutics and prognosis of solid tumours.

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10.  Butyrate directly decreases human gut lamina propria CD4 T cell function through histone deacetylase (HDAC) inhibition and GPR43 signaling.

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