Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.

Multiple myeloma (MM) is a plasma cell malignancy that is heterogeneous in its clinical presentation and prognosis. Monoclonal gammopathy of undetermined significance (MGUS) consistently preceded development of MM. The presence of primary IgH translocations and the universal over-expression of cycli...

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Main Authors: Patricia eGomez-Bougie, Martine eAmiot
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-12-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00467/full
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author Patricia eGomez-Bougie
Patricia eGomez-Bougie
Martine eAmiot
author_facet Patricia eGomez-Bougie
Patricia eGomez-Bougie
Martine eAmiot
author_sort Patricia eGomez-Bougie
collection DOAJ
description Multiple myeloma (MM) is a plasma cell malignancy that is heterogeneous in its clinical presentation and prognosis. Monoclonal gammopathy of undetermined significance (MGUS) consistently preceded development of MM. The presence of primary IgH translocations and the universal over-expression of cyclin D genes led to a molecular classification of MM patients into different disease subtypes. Since Bcl-2 family proteins determine cell fate, we analyzed a publicly available Affymetrix gene expression of 44 MGUS and 414 newly diagnosed MM patients to investigate (1) the global change of Bcl-2 family members in MM versus MGUS (2) whether the four major subtypes defined as hyperdiploid, CCND1, MAF and MMSET, display specific apoptotic machineries.<br/>We showed that among the main anti-apoptotic members (Bcl-2, Bcl-xL and Mcl-1), Mcl-1 up-regulation discriminated MM from MGUS, in agreement with the prominent role of Mcl-1 in plasma cell differentiation. Surprisingly, the expression of multi-domain pro-apoptotic Bak and Bax were increased during the progression of MGUS to MM. The combined profile of Bcl-2, Bcl-xL and Mcl-1 was sufficient to distinguish MM molecular groups. While specific pro-apoptotic members expression was observed for each MM subtypes, CCDN1 subgroup, was identified as a particular entity characterized by a low expression of both BH3-only (Puma, Bik and Bad) and multi-domain pro-apoptotic members (Bax and Bak). Our analysis supports the notion that MM heterogeneity is extended to the differential expression of the Bcl-2 family content in each MM subgroup. The influence of Bcl-2 family profile in the survival of the different patient groups will be further discussed to establish the potential consequences for therapeutic interventions. Finally, the use of distinct pro-survival members in the different steps of immune responses to antigen rise also the question of whether the different Bcl-2 anti-apoptotic profile could reflect a different origin of MM cells. <br/>
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spelling doaj.art-5d0bcba3a2b0432f996a65c123d697a52022-12-22T00:21:17ZengFrontiers Media S.A.Frontiers in Immunology1664-32242013-12-01410.3389/fimmu.2013.0046770600Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.Patricia eGomez-Bougie0Patricia eGomez-Bougie1Martine eAmiot2CNRSCHU de NantesCNRSMultiple myeloma (MM) is a plasma cell malignancy that is heterogeneous in its clinical presentation and prognosis. Monoclonal gammopathy of undetermined significance (MGUS) consistently preceded development of MM. The presence of primary IgH translocations and the universal over-expression of cyclin D genes led to a molecular classification of MM patients into different disease subtypes. Since Bcl-2 family proteins determine cell fate, we analyzed a publicly available Affymetrix gene expression of 44 MGUS and 414 newly diagnosed MM patients to investigate (1) the global change of Bcl-2 family members in MM versus MGUS (2) whether the four major subtypes defined as hyperdiploid, CCND1, MAF and MMSET, display specific apoptotic machineries.<br/>We showed that among the main anti-apoptotic members (Bcl-2, Bcl-xL and Mcl-1), Mcl-1 up-regulation discriminated MM from MGUS, in agreement with the prominent role of Mcl-1 in plasma cell differentiation. Surprisingly, the expression of multi-domain pro-apoptotic Bak and Bax were increased during the progression of MGUS to MM. The combined profile of Bcl-2, Bcl-xL and Mcl-1 was sufficient to distinguish MM molecular groups. While specific pro-apoptotic members expression was observed for each MM subtypes, CCDN1 subgroup, was identified as a particular entity characterized by a low expression of both BH3-only (Puma, Bik and Bad) and multi-domain pro-apoptotic members (Bax and Bak). Our analysis supports the notion that MM heterogeneity is extended to the differential expression of the Bcl-2 family content in each MM subgroup. The influence of Bcl-2 family profile in the survival of the different patient groups will be further discussed to establish the potential consequences for therapeutic interventions. Finally, the use of distinct pro-survival members in the different steps of immune responses to antigen rise also the question of whether the different Bcl-2 anti-apoptotic profile could reflect a different origin of MM cells. <br/>http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00467/fullMultiple MyelomaPlasma CellsBCL-2 FamilyMGUSMolecular myeloma subgroups
spellingShingle Patricia eGomez-Bougie
Patricia eGomez-Bougie
Martine eAmiot
Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.
Frontiers in Immunology
Multiple Myeloma
Plasma Cells
BCL-2 Family
MGUS
Molecular myeloma subgroups
title Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.
title_full Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.
title_fullStr Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.
title_full_unstemmed Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.
title_short Apoptotic machinery diversity in Multiple Myeloma molecular subtypes.
title_sort apoptotic machinery diversity in multiple myeloma molecular subtypes
topic Multiple Myeloma
Plasma Cells
BCL-2 Family
MGUS
Molecular myeloma subgroups
url http://journal.frontiersin.org/Journal/10.3389/fimmu.2013.00467/full
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