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Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man
The Prostate Cancer Foundation-Movember Foundation Reproducibility Initiative (PCFMFRI) seeks to address growing concerns about reproducibility in scientific research by conducting replications of recent papers in the field of prostate cancer. This Registered Report describes the proposed replicatio...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579027/ https://www.ncbi.nlm.nih.gov/pubmed/26401447 http://dx.doi.org/10.7717/peerj.1231 |
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author | Chronscinski, Denise Cherukeri, Srujana Tan, Fraser Perfito, Nicole Lomax, Joelle Iorns, Elizabeth |
author_facet | Chronscinski, Denise Cherukeri, Srujana Tan, Fraser Perfito, Nicole Lomax, Joelle Iorns, Elizabeth |
author_sort | Chronscinski, Denise |
collection | PubMed |
description | The Prostate Cancer Foundation-Movember Foundation Reproducibility Initiative (PCFMFRI) seeks to address growing concerns about reproducibility in scientific research by conducting replications of recent papers in the field of prostate cancer. This Registered Report describes the proposed replication plan of key experiments from “The Androgen Receptor Induces a Distinct Transcriptional Program in Castration-Resistant Prostate Cancer in Man” by Sharma and colleagues (2013), published in Cancer Cell in 2013. Of thousands of targets for the androgen receptor (AR), the authors elucidated a subset of 16 core genes that were consistently downregulated with castration and re-emerged with castration resistance. These 16 AR binding sites were distinct from those observed in cells in culture. The authors suggested that cellular context can have dramatic effects on downstream transcriptional regulation of AR binding sites. The present study will attempt to replicate Fig. 7C by comparing gene expression of the 16 core genes identified by Sharma and colleagues in xenograft tumor tissue compared to androgen treated LNCaP cells in vitro. The Prostate Cancer Foundation-Movember Foundation Reproducibility Initiative is a collaboration between the Prostate Cancer Foundation, the Movember Initiative, and Science Exchange, and the results of the replications will be published by PeerJ. |
format | Online Article Text |
id | pubmed-4579027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-45790272015-09-23 Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man Chronscinski, Denise Cherukeri, Srujana Tan, Fraser Perfito, Nicole Lomax, Joelle Iorns, Elizabeth PeerJ Cell Biology The Prostate Cancer Foundation-Movember Foundation Reproducibility Initiative (PCFMFRI) seeks to address growing concerns about reproducibility in scientific research by conducting replications of recent papers in the field of prostate cancer. This Registered Report describes the proposed replication plan of key experiments from “The Androgen Receptor Induces a Distinct Transcriptional Program in Castration-Resistant Prostate Cancer in Man” by Sharma and colleagues (2013), published in Cancer Cell in 2013. Of thousands of targets for the androgen receptor (AR), the authors elucidated a subset of 16 core genes that were consistently downregulated with castration and re-emerged with castration resistance. These 16 AR binding sites were distinct from those observed in cells in culture. The authors suggested that cellular context can have dramatic effects on downstream transcriptional regulation of AR binding sites. The present study will attempt to replicate Fig. 7C by comparing gene expression of the 16 core genes identified by Sharma and colleagues in xenograft tumor tissue compared to androgen treated LNCaP cells in vitro. The Prostate Cancer Foundation-Movember Foundation Reproducibility Initiative is a collaboration between the Prostate Cancer Foundation, the Movember Initiative, and Science Exchange, and the results of the replications will be published by PeerJ. PeerJ Inc. 2015-09-15 /pmc/articles/PMC4579027/ /pubmed/26401447 http://dx.doi.org/10.7717/peerj.1231 Text en © 2015 Chronscinski et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Cell Biology Chronscinski, Denise Cherukeri, Srujana Tan, Fraser Perfito, Nicole Lomax, Joelle Iorns, Elizabeth Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man |
title | Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man |
title_full | Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man |
title_fullStr | Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man |
title_full_unstemmed | Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man |
title_short | Registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man |
title_sort | registered report: the androgen receptor induces a distinct transcriptional program in castration-resistant prostate cancer in man |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579027/ https://www.ncbi.nlm.nih.gov/pubmed/26401447 http://dx.doi.org/10.7717/peerj.1231 |
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