Interferon-γ-induced upregulation of immunoproteasome subunit assembly overcomes bortezomib resistance in human hematological cell linesReport as inadecuate




Interferon-γ-induced upregulation of immunoproteasome subunit assembly overcomes bortezomib resistance in human hematological cell lines - Download this document for free, or read online. Document in PDF available to download.

Journal of Hematology and Oncology

, 7:7

First Online: 13 January 2014Received: 16 October 2013Accepted: 06 January 2014DOI: 10.1186-1756-8722-7-7

Cite this article as: Niewerth, D., Kaspers, G.J., Assaraf, Y.G. et al. J Hematol Oncol 2014 7: 7. doi:10.1186-1756-8722-7-7

Abstract

BackgroundDespite encouraging results with the proteasome inhibitor bortezomib in the treatment of hematologic malignancies, emergence of resistance can limit its efficacy, hence calling for novel strategies to overcome bortezomib-resistance. We previously showed that bortezomib-resistant human leukemia cell lines expressed significantly lower levels of immunoproteasome at the expense of constitutive proteasomes, which harbored point mutations in exon 2 of the PSMB5 gene encoding the β5 subunit. Here we investigated whether up-regulation of immunoproteasomes by exposure to interferon-γ restores sensitivity to bortezomib in myeloma and leukemia cell lines with acquired resistance to bortezomib.

MethodsRPMI-8226 myeloma, THP1 monocytic-macrophage and CCRF-CEM T parental cells and sub lines with acquired resistance to bortezomib were exposed to Interferon-γ for 24-48 h where after the effects on proteasome subunit expression and activity were measured, next to sensitivity measurements to proteasome inhibitors bortezomib, carfilzomib, and the immunoproteasome selective inhibitor ONX 0914. At last, siRNA knockdown experiments of β5i and β1i were performed to identify the contribution of these subunits to sensitivity to proteasome inhibition. Statistical significance of the differences were determined using the Mann-Whitney U test.

ResultsInterferon-γ exposure markedly increased immunoproteasome subunit mRNA to a significantly higher level in bortezomib-resistant cells up to 30-fold, 10-fold, and 6-fold, in β1i, β5i, and β2i, respectively than in parental cells. These increases were paralleled by elevated immunoproteasome protein levels and catalytic activity, as well as HLA class-I. Moreover, interferon-γ exposure reinforced sensitization of bortezomib-resistant tumor cells to bortezomib and carfilzomib, but most prominently to ONX 0914, as confirmed by cell growth inhibition studies, proteasome inhibitor-induced apoptosis, activation of PARP cleavage and accumulation of polyubiquitinated proteins. This sensitization was abrogated by siRNA silencing of β5i but not by β1i silencing, prior to pulse exposure to interferon-γ.

ConclusionDownregulation of β5i subunit expression is a major determinant in acquisition of bortezomib-resistance and enhancement of its proteasomal assembly after induction by interferon-γ facilitates restoration of sensitivity in bortezomib-resistant leukemia cells towards bortezomib and next generation immuno proteasome inhibitors.

KeywordsLeukemia Proteasome Immunoproteasome Proteasome inhibitor Bortezomib Interferon-gamma Electronic supplementary materialThe online version of this article doi:10.1186-1756-8722-7-7 contains supplementary material, which is available to authorized users.

Gerrit Jansen and Jacqueline Cloos contributed equally to this work.

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Author: Denise Niewerth - Gertjan JL Kaspers - Yehuda G Assaraf - Johan van Meerloo - Christopher J Kirk - Janet Anderl - Jonatha

Source: https://link.springer.com/







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