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Deciphering the chronology of copy number alterations in Multiple Myeloma
Multiple myeloma (MM) and its precursor condition MGUS are characterized by chromosomal aberrations. Here, we comprehensively characterize the order of occurrence of these complex genomic events underlying MM development using 500 MGUS, and MM samples. We identify hyperdiploid MM (HMM) and non-HMM a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435669/ https://www.ncbi.nlm.nih.gov/pubmed/30914633 http://dx.doi.org/10.1038/s41408-019-0199-3 |
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author | Aktas Samur, Anil Minvielle, Stephane Shammas, Masood Fulciniti, Mariateresa Magrangeas, Florence Richardson, Paul G. Moreau, Philippe Attal, Michel Anderson, Kenneth C. Parmigiani, Giovanni Avet-Loiseau, Hervé Munshi, Nikhil C. Samur, Mehmet Kemal |
author_facet | Aktas Samur, Anil Minvielle, Stephane Shammas, Masood Fulciniti, Mariateresa Magrangeas, Florence Richardson, Paul G. Moreau, Philippe Attal, Michel Anderson, Kenneth C. Parmigiani, Giovanni Avet-Loiseau, Hervé Munshi, Nikhil C. Samur, Mehmet Kemal |
author_sort | Aktas Samur, Anil |
collection | PubMed |
description | Multiple myeloma (MM) and its precursor condition MGUS are characterized by chromosomal aberrations. Here, we comprehensively characterize the order of occurrence of these complex genomic events underlying MM development using 500 MGUS, and MM samples. We identify hyperdiploid MM (HMM) and non-HMM as genomically distinct entities with different evolution of the copy number alterations. In HMM, gains of 9,15 or 19 are the first and clonal events observed as clonal even at MGUS stage. These events are thus early and may underlie initial transformation of normal plasma cells to MGUS cells. However, CNAs may not be adequate for progression to MM except in 15% of the patients in whom the complex subclonal deletion events are observed in MM but not MGUS. In NHMM, besides the driver translocations, clonal deletion of 13 and 1q gain are early events also observed in MGUS. We combined this information to propose a timeline for copy number alteration. |
format | Online Article Text |
id | pubmed-6435669 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64356692019-03-27 Deciphering the chronology of copy number alterations in Multiple Myeloma Aktas Samur, Anil Minvielle, Stephane Shammas, Masood Fulciniti, Mariateresa Magrangeas, Florence Richardson, Paul G. Moreau, Philippe Attal, Michel Anderson, Kenneth C. Parmigiani, Giovanni Avet-Loiseau, Hervé Munshi, Nikhil C. Samur, Mehmet Kemal Blood Cancer J Article Multiple myeloma (MM) and its precursor condition MGUS are characterized by chromosomal aberrations. Here, we comprehensively characterize the order of occurrence of these complex genomic events underlying MM development using 500 MGUS, and MM samples. We identify hyperdiploid MM (HMM) and non-HMM as genomically distinct entities with different evolution of the copy number alterations. In HMM, gains of 9,15 or 19 are the first and clonal events observed as clonal even at MGUS stage. These events are thus early and may underlie initial transformation of normal plasma cells to MGUS cells. However, CNAs may not be adequate for progression to MM except in 15% of the patients in whom the complex subclonal deletion events are observed in MM but not MGUS. In NHMM, besides the driver translocations, clonal deletion of 13 and 1q gain are early events also observed in MGUS. We combined this information to propose a timeline for copy number alteration. Nature Publishing Group UK 2019-03-26 /pmc/articles/PMC6435669/ /pubmed/30914633 http://dx.doi.org/10.1038/s41408-019-0199-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Aktas Samur, Anil Minvielle, Stephane Shammas, Masood Fulciniti, Mariateresa Magrangeas, Florence Richardson, Paul G. Moreau, Philippe Attal, Michel Anderson, Kenneth C. Parmigiani, Giovanni Avet-Loiseau, Hervé Munshi, Nikhil C. Samur, Mehmet Kemal Deciphering the chronology of copy number alterations in Multiple Myeloma |
title | Deciphering the chronology of copy number alterations in Multiple Myeloma |
title_full | Deciphering the chronology of copy number alterations in Multiple Myeloma |
title_fullStr | Deciphering the chronology of copy number alterations in Multiple Myeloma |
title_full_unstemmed | Deciphering the chronology of copy number alterations in Multiple Myeloma |
title_short | Deciphering the chronology of copy number alterations in Multiple Myeloma |
title_sort | deciphering the chronology of copy number alterations in multiple myeloma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435669/ https://www.ncbi.nlm.nih.gov/pubmed/30914633 http://dx.doi.org/10.1038/s41408-019-0199-3 |
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