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Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma

Human multiple myeloma (MM) is characterized by accumulation of malignant terminally differentiated plasma cells (PCs) in the bone marrow (BM), raising the question when during maturation neoplastic transformation begins. Immunoglobulin IGHV genes carry imprints of clonal tumor history, delineating...

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Autores principales: Cowan, Graeme, Weston-Bell, Nicola J., Bryant, Dean, Seckinger, Anja, Hose, Dirk, Zojer, Niklas, Sahota, Surinder S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537010/
https://www.ncbi.nlm.nih.gov/pubmed/25929340
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author Cowan, Graeme
Weston-Bell, Nicola J.
Bryant, Dean
Seckinger, Anja
Hose, Dirk
Zojer, Niklas
Sahota, Surinder S.
author_facet Cowan, Graeme
Weston-Bell, Nicola J.
Bryant, Dean
Seckinger, Anja
Hose, Dirk
Zojer, Niklas
Sahota, Surinder S.
author_sort Cowan, Graeme
collection PubMed
description Human multiple myeloma (MM) is characterized by accumulation of malignant terminally differentiated plasma cells (PCs) in the bone marrow (BM), raising the question when during maturation neoplastic transformation begins. Immunoglobulin IGHV genes carry imprints of clonal tumor history, delineating somatic hypermutation (SHM) events that generally occur in the germinal center (GC). Here, we examine MM-derived IGHV genes using massive parallel deep sequencing, comparing them with profiles in normal BM PCs. In 4/4 presentation IgG MM, monoclonal tumor-derived IGHV sequences revealed significant evidence for intraclonal variation (ICV) in mutation patterns. IGHV sequences of 2/2 normal PC IgG populations revealed dominant oligoclonal expansions, each expansion also displaying mutational ICV. Clonal expansions in MM and in normal BM PCs reveal common IGHV features. In such MM, the data fit a model of tumor origins in which neoplastic transformation is initiated in a GC B-cell committed to terminal differentiation but still targeted by on-going SHM. Strikingly, the data parallel IGHV clonal sequences in some monoclonal gammopathy of undetermined significance (MGUS) known to display on-going SHM imprints. Since MGUS generally precedes MM, these data suggest origins of MGUS and MM with IGHV gene mutational ICV from the same GC B-cell, arising via a distinctive pathway.
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spelling pubmed-45370102015-08-26 Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma Cowan, Graeme Weston-Bell, Nicola J. Bryant, Dean Seckinger, Anja Hose, Dirk Zojer, Niklas Sahota, Surinder S. Oncotarget Research Paper Human multiple myeloma (MM) is characterized by accumulation of malignant terminally differentiated plasma cells (PCs) in the bone marrow (BM), raising the question when during maturation neoplastic transformation begins. Immunoglobulin IGHV genes carry imprints of clonal tumor history, delineating somatic hypermutation (SHM) events that generally occur in the germinal center (GC). Here, we examine MM-derived IGHV genes using massive parallel deep sequencing, comparing them with profiles in normal BM PCs. In 4/4 presentation IgG MM, monoclonal tumor-derived IGHV sequences revealed significant evidence for intraclonal variation (ICV) in mutation patterns. IGHV sequences of 2/2 normal PC IgG populations revealed dominant oligoclonal expansions, each expansion also displaying mutational ICV. Clonal expansions in MM and in normal BM PCs reveal common IGHV features. In such MM, the data fit a model of tumor origins in which neoplastic transformation is initiated in a GC B-cell committed to terminal differentiation but still targeted by on-going SHM. Strikingly, the data parallel IGHV clonal sequences in some monoclonal gammopathy of undetermined significance (MGUS) known to display on-going SHM imprints. Since MGUS generally precedes MM, these data suggest origins of MGUS and MM with IGHV gene mutational ICV from the same GC B-cell, arising via a distinctive pathway. Impact Journals LLC 2015-04-10 /pmc/articles/PMC4537010/ /pubmed/25929340 Text en Copyright: © 2015 Cowan et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Cowan, Graeme
Weston-Bell, Nicola J.
Bryant, Dean
Seckinger, Anja
Hose, Dirk
Zojer, Niklas
Sahota, Surinder S.
Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma
title Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma
title_full Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma
title_fullStr Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma
title_full_unstemmed Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma
title_short Massive parallel IGHV gene sequencing reveals a germinal center pathway in origins of human multiple myeloma
title_sort massive parallel ighv gene sequencing reveals a germinal center pathway in origins of human multiple myeloma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537010/
https://www.ncbi.nlm.nih.gov/pubmed/25929340
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