Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemia

The Reproducibility Project: Cancer Biology seeks to address growing concerns about reproducibility in scientific research by conducting replications of selected experiments from a number of high-profile papers in the field of cancer biology. The papers, which were published between 2010 and 2012, w...

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Main Authors: Juan José Fung, Alan Kosaka, Xiaochuan Shan, Gwenn Danet-Desnoyers, Michael Gormally, Kate Owen, Reproducibility Project: Cancer Biology
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2015-09-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/08997
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spelling doaj-4d0c8be0eaf9468bb6f9d45c14d1e5eb2021-05-04T23:59:50ZengeLife Sciences Publications LtdeLife2050-084X2015-09-01410.7554/eLife.08997Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemiaJuan José Fung0Alan Kosaka1Xiaochuan Shan2Gwenn Danet-Desnoyers3Michael Gormally4Kate Owen5Reproducibility Project: Cancer BiologyProNovus Bioscience, Mountain View, CaliforniaProNovus Bioscience, Mountain View, CaliforniaStem Cell and Xenograft Core, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PennsylvaniaStem Cell and Xenograft Core, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PennsylvaniaUniversity of Cambridge, Cambridge, United KingdomUniversity of Virginia, Charlottesville, VirginiaThe Reproducibility Project: Cancer Biology seeks to address growing concerns about reproducibility in scientific research by conducting replications of selected experiments from a number of high-profile papers in the field of cancer biology. The papers, which were published between 2010 and 2012, were selected on the basis of citations and Altmetric scores (Errington et al., 2014). This Registered report describes the proposed replication plan of key experiments from ‘Inhibition of bromodomain and extra terminal (BET) recruitment to chromatin as an effective treatment for mixed-lineage leukemia (MLL)-fusion leukemia’ by Dawson and colleagues, published in Nature in 2011 (Dawson et al., 2011). The experiments to be replicated are those reported in Figures 2A, 3D, 4B, 4D and Supplementary Figures 11A-B and 16A. In this study, BET proteins were demonstrated as potential therapeutic targets for modulating aberrant gene expression programs associated with MLL-fusion leukemia. In Figure 2A, the BET bromodomain inhibitor I-BET151 was reported to suppress growth of cells harboring MLL-fusions compared to those with alternate oncogenic drivers. In Figure 3D, treatment of MLL-fusion leukemia cells with I-BET151 resulted in transcriptional suppression of the anti-apoptotic gene BCL2. Figures 4B and 4D tested the therapeutic efficacy of I-BET151 in vivo using mice injected with human MLL-fusion leukemia cells and evaluated disease progression following I-BET151 treatment. The Reproducibility Project: Cancer Biology is a collaboration between the Center for Open Science and Science Exchange and the results of the replications will be published in eLife.https://elifesciences.org/articles/08997Reproducibility Project: Cancer Biologymethodologybromodomain inhibitorleukemia
collection DOAJ
language English
format Article
sources DOAJ
author Juan José Fung
Alan Kosaka
Xiaochuan Shan
Gwenn Danet-Desnoyers
Michael Gormally
Kate Owen
Reproducibility Project: Cancer Biology
spellingShingle Juan José Fung
Alan Kosaka
Xiaochuan Shan
Gwenn Danet-Desnoyers
Michael Gormally
Kate Owen
Reproducibility Project: Cancer Biology
Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemia
eLife
Reproducibility Project: Cancer Biology
methodology
bromodomain inhibitor
leukemia
author_facet Juan José Fung
Alan Kosaka
Xiaochuan Shan
Gwenn Danet-Desnoyers
Michael Gormally
Kate Owen
Reproducibility Project: Cancer Biology
author_sort Juan José Fung
title Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemia
title_short Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemia
title_full Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemia
title_fullStr Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemia
title_full_unstemmed Registered report: Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukemia
title_sort registered report: inhibition of bet recruitment to chromatin as an effective treatment for mll-fusion leukemia
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2015-09-01
description The Reproducibility Project: Cancer Biology seeks to address growing concerns about reproducibility in scientific research by conducting replications of selected experiments from a number of high-profile papers in the field of cancer biology. The papers, which were published between 2010 and 2012, were selected on the basis of citations and Altmetric scores (Errington et al., 2014). This Registered report describes the proposed replication plan of key experiments from ‘Inhibition of bromodomain and extra terminal (BET) recruitment to chromatin as an effective treatment for mixed-lineage leukemia (MLL)-fusion leukemia’ by Dawson and colleagues, published in Nature in 2011 (Dawson et al., 2011). The experiments to be replicated are those reported in Figures 2A, 3D, 4B, 4D and Supplementary Figures 11A-B and 16A. In this study, BET proteins were demonstrated as potential therapeutic targets for modulating aberrant gene expression programs associated with MLL-fusion leukemia. In Figure 2A, the BET bromodomain inhibitor I-BET151 was reported to suppress growth of cells harboring MLL-fusions compared to those with alternate oncogenic drivers. In Figure 3D, treatment of MLL-fusion leukemia cells with I-BET151 resulted in transcriptional suppression of the anti-apoptotic gene BCL2. Figures 4B and 4D tested the therapeutic efficacy of I-BET151 in vivo using mice injected with human MLL-fusion leukemia cells and evaluated disease progression following I-BET151 treatment. The Reproducibility Project: Cancer Biology is a collaboration between the Center for Open Science and Science Exchange and the results of the replications will be published in eLife.
topic Reproducibility Project: Cancer Biology
methodology
bromodomain inhibitor
leukemia
url https://elifesciences.org/articles/08997
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