Spectrum and functional validation of PSMB5 mutations in multiple myeloma

Barrio S, Stuehmer T, Da-Via M, Barrio-Garcia C, Lehners N, Besse A, Cuenca I, Garitano-Trojaola A, Fink S, Leich E, Chatterjee M, Driessen C, Martinez-Lopez J, Rosenwald A, Beckmann R, Bargou RC, Braggio E, Stewart AK, Raab MS, Einsele H, Kortuem KM (2019)


Publication Type: Journal article

Publication year: 2019

Journal

Book Volume: 33

Pages Range: 447-456

Journal Issue: 2

DOI: 10.1038/s41375-018-0216-8

Abstract

Despite an increasing number of approved therapies, multiple myeloma (MM) remains an incurable disease and only a small number of patients achieve prolonged disease control. Some genes have been linked with response to commonly used anti-MM compounds, including immunomodulators (IMiDs) and proteasome inhibitors (PIs). In this manuscript, we demonstrate an increased incidence of acquired proteasomal subunit mutations in relapsed MM compared to newly diagnosed disease, underpinning a potential role of point mutations in the clonal evolution of MM. Furthermore, we are first to present and functionally characterize four somatic PSMB5 mutations from primary MM cells identified in a patient under prolonged proteasome inhibition, with three of them affecting the PI-binding pocket S1. We confirm resistance induction through missense mutations not only to Bortezomib, but also, in variable extent, to the next-generation PIs Carfilzomib and Ixazomib. In addition, a negative impact on the proteasome activity is assessed, providing a potential explanation for later therapy-induced eradication of the affected tumor subclones in this patient.

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How to cite

APA:

Barrio, S., Stuehmer, T., Da-Via, M., Barrio-Garcia, C., Lehners, N., Besse, A.,... Kortuem, K.M. (2019). Spectrum and functional validation of PSMB5 mutations in multiple myeloma. Leukemia, 33(2), 447-456. https://doi.org/10.1038/s41375-018-0216-8

MLA:

Barrio, Santiago, et al. "Spectrum and functional validation of PSMB5 mutations in multiple myeloma." Leukemia 33.2 (2019): 447-456.

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