Journal article
TRPM4 expression is associated with activated B-cell subtype and poor survival in diffuse large B-cell lymphoma
- Abstract:
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Aims
Transient receptor potential channel melastatin 4 (TRPM4) is an ion channel that regulates influx of calcium cations (Ca2+). Recent studies suggest that TRPM4 is an oncoprotein and its upregulated transcript level has been reported in diffuse large B-cell lymphoma (DLBCL). We aim to investigate TRPM4 protein expression pattern in non-malignant tissues and DLBCL cases, and its association with clinico-demographical parameters and survival in DLBCL.
Methods and results
Analysis of publicly-available DLBCL microarray datasets showed that TRPM4 transcripts were upregulated in DLBCL compared to normal germinal centre B (GCB) cells, were more highly expressed in the activated B-cell-like DLBCL (ABC-DLBCL) subtype, and higher TRPM4 transcripts conferred worse overall survival (OS) in R-CHOP-treated DLBCL cases (P<0.05). Our immunohistochemical analysis showed that TRPM4 was expressed in various human tissues but not in normal B cells within lymphoid tissues (reactive tonsil, lymph node and appendix). TRPM4 protein was present in 26% (n=49/189) of our cohort of R-CHOP-treated DLBCL cases and this was significantly associated with more aggressive clinical parameters including higher LDH, ECOG scores or stage (P<0.01 for each of the parameter) and the ABC-DLBCL subtype (P=0.016). TRPM4 positivity conferred significantly worse OS (P=0.004) and PFS (P=0.005). Worse OS remained significantly associated with TRPM4 positivity in multivariate analysis including higher international prognostic index (IPI) or the non-GCB DLBCL phenotype (P<0.05).
Conclusions
TRPM4 protein expression is upregulated in DLBCL cases compared to non-malignant B cells with preferential expression in ABC-DLBCL cases, and it confers significantly poorer DLBCL patients’ outcomes.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 508.6KB, Terms of use)
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(Preview, Accepted manuscript, pdf, 1.3MB, Terms of use)
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- Publisher copy:
- 10.1111/his.13204
Authors
- Publisher:
- Wiley
- Journal:
- Histopathology More from this journal
- Publication date:
- 2017-03-01
- Acceptance date:
- 2017-02-23
- DOI:
- ISSN:
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1365-2559
- Keywords:
- Pubs id:
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pubs:685222
- UUID:
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uuid:5ea94e06-3bbd-4e08-b202-68e0757453f9
- Local pid:
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pubs:685222
- Source identifiers:
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685222
- Deposit date:
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2017-03-10
Terms of use
- Copyright holder:
- John Wiley and Sons Ltd
- Copyright date:
- 2017
- Notes:
- © 2017 John Wiley and Sons Ltd
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