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Regulation of Transient Site-specific Copy Gain by MicroRNA

Intra-tumor copy number heterogeneity is commonly observed in cancer; however, the molecular mechanisms that contribute to heterogeneity remain poorly understood. Up-regulation of the histone demethylase KDM4A promotes transient site-specific copy gain (TSSG) in cells; therefore, uncovering how KDM4...

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Autores principales: Black, Joshua C., Zhang, Hailei, Kim, Jaegil, Getz, Gad, Whetstine, Johnathan R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777823/
https://www.ncbi.nlm.nih.gov/pubmed/26755726
http://dx.doi.org/10.1074/jbc.M115.711648
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author Black, Joshua C.
Zhang, Hailei
Kim, Jaegil
Getz, Gad
Whetstine, Johnathan R.
author_facet Black, Joshua C.
Zhang, Hailei
Kim, Jaegil
Getz, Gad
Whetstine, Johnathan R.
author_sort Black, Joshua C.
collection PubMed
description Intra-tumor copy number heterogeneity is commonly observed in cancer; however, the molecular mechanisms that contribute to heterogeneity remain poorly understood. Up-regulation of the histone demethylase KDM4A promotes transient site-specific copy gain (TSSG) in cells; therefore, uncovering how KDM4A levels are controlled is important for understanding the regulation of copy number heterogeneity. Here, we demonstrate that KDM4A is regulated by hsa-mir-23a-3p, hsa-mir-23b-3p, and hsa-mir-137. Altering expression of these microRNAs (miRNAs) regulates KDM4A-dependent TSSG. miRNA inhibition promoted copy gains and increased expression of the drug-resistant oncogene CKS1B, which was further substantiated in primary breast tumors. Consistent with increased CKS1B expression, miRNA inhibition reduced breast cancer cell sensitivity to cisplatin. Our data identify these miRNAs as regulators of TSSG and copy gains of a drug resistance gene.
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spelling pubmed-47778232016-03-10 Regulation of Transient Site-specific Copy Gain by MicroRNA Black, Joshua C. Zhang, Hailei Kim, Jaegil Getz, Gad Whetstine, Johnathan R. J Biol Chem DNA and Chromosomes Intra-tumor copy number heterogeneity is commonly observed in cancer; however, the molecular mechanisms that contribute to heterogeneity remain poorly understood. Up-regulation of the histone demethylase KDM4A promotes transient site-specific copy gain (TSSG) in cells; therefore, uncovering how KDM4A levels are controlled is important for understanding the regulation of copy number heterogeneity. Here, we demonstrate that KDM4A is regulated by hsa-mir-23a-3p, hsa-mir-23b-3p, and hsa-mir-137. Altering expression of these microRNAs (miRNAs) regulates KDM4A-dependent TSSG. miRNA inhibition promoted copy gains and increased expression of the drug-resistant oncogene CKS1B, which was further substantiated in primary breast tumors. Consistent with increased CKS1B expression, miRNA inhibition reduced breast cancer cell sensitivity to cisplatin. Our data identify these miRNAs as regulators of TSSG and copy gains of a drug resistance gene. American Society for Biochemistry and Molecular Biology 2016-03-04 2016-01-11 /pmc/articles/PMC4777823/ /pubmed/26755726 http://dx.doi.org/10.1074/jbc.M115.711648 Text en © 2016 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version free via Creative Commons CC-BY license (http://creativecommons.org/licenses/by/4.0) .
spellingShingle DNA and Chromosomes
Black, Joshua C.
Zhang, Hailei
Kim, Jaegil
Getz, Gad
Whetstine, Johnathan R.
Regulation of Transient Site-specific Copy Gain by MicroRNA
title Regulation of Transient Site-specific Copy Gain by MicroRNA
title_full Regulation of Transient Site-specific Copy Gain by MicroRNA
title_fullStr Regulation of Transient Site-specific Copy Gain by MicroRNA
title_full_unstemmed Regulation of Transient Site-specific Copy Gain by MicroRNA
title_short Regulation of Transient Site-specific Copy Gain by MicroRNA
title_sort regulation of transient site-specific copy gain by microrna
topic DNA and Chromosomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777823/
https://www.ncbi.nlm.nih.gov/pubmed/26755726
http://dx.doi.org/10.1074/jbc.M115.711648
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