Evidence map›Paper›PMID 27307990›Full record

ArticleBiomarker research2016

The CXCR4 antagonist plerixafor enhances the effect of rituximab in diffuse large B-cell lymphoma cell lines.

Linn Reinholdt, Maria Bach Laursen, Alexander Schmitz, Julie Støve Bødker, Lasse Hjort Jakobsen, Martin Bøgsted, Hans Erik Johnsen, Karen Dybkær

Open access · goldAbstract read
In one paragraph

Article in Biomarker research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
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  4. GPCR Inhibition in Treating Lymphoma.ACS medicinal chemistry letters · 2022
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  9. Review
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  17. Small Molecules Drive Big Improvements in Immuno-Oncology Therapies.Angewandte Chemie (International ed. in English) · 2018
    Review
  18. Review
  19. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Linn ReinholdtDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Maria Bach LaursenDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Alexander SchmitzDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Clinical Cancer Research Center, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Julie Støve BødkerDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Clinical Cancer Research Center, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Lasse Hjort JakobsenDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Department of Clinical Medicine, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Martin BøgstedDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Clinical Cancer Research Center, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Department of Clinical Medicine, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Hans Erik JohnsenDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Clinical Cancer Research Center, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Department of Clinical Medicine, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Karen DybkærDepartment of Haematology, Aalborg University Hospital, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Clinical Cancer Research Center, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark ; Department of Clinical Medicine, Aalborg University, Sdr Skovvej 15, Aalborg, DK-9000 Denmark.
Aalborg University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiffuse large B-cell lymphoma (DLBCL) is an aggressive disease with variable clinical outcome, accounting for at least 25-30 % of adult non-Hodgkin lymphomas. Approximately one third of DLBCL patients are not cured by the currently used treatment regimen, R-CHOP. Hence, new treatment strategies are needed. Antagonizing the CXCR4 receptor might be promising since the CXCR4-CXCL12 axis is implicated in several aspects of tumor pathogenesis as well as in protection from chemotherapeutic response. In Burkitt lymphoma, the CXCR4 antagonist plerixafor has already been shown to enhance the therapeutic effect of rituximab, the immunotherapeutic agent of R-CHOP; but this is yet to be confirmed for DLBCL. We, therefore, investigated the effect of plerixafor on DLBCL cellular response to rituximab.

methodsIn this in vitro study, human DLBCL cell lines were treated with rituximab and/or plerixafor, concomitantly or in sequence. The trypan blue exclusion method and MTS-based assays were used to evaluate cellular proliferation, whereas flow cytometry was used for assessment of apoptosis status and CXCR4 surface expression level. Linear mixed effects models were used to assess statistical significance.

resultsWe observed that simultaneous addition of plerixafor and rituximab resulted in a significant decrease in DLBCL cellular proliferation, compared to monotherapeutic response. The effect was dose-dependent, and concomitant administration was observed to be superior to sequential drug administration. Accordingly, the fraction of apoptotic/dead cells significantly increased following addition of plerixafor to rituximab treatment. Furthermore, exposure of DLBCL cells to plerixafor resulted in a significant decrease in CXCR4 fluorescence intensity.

conclusionsBased on our results, implying that the anti-proliferative/pro-apoptotic effect of rituximab on DLBCL cells can be synergistically enhanced by the CXCR4 antagonist plerixafor, addition of plerixafor to the R-CHOP regimen can be suggested to improve treatment outcome for DLBCL patients.

Indexed as

AMD3100Anti-CD20 antibodyCXCR4CXCR4 antagonistDiffuse large B-cell lymphomaDLBCLDrug combination studyin vitroPlerixaforRituximab

Identifiers

PMID27307990
PMCPMC4908729
OpenAlexW2438619479

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.