Evidence map›Paper›PMID 28196522›Full record

ReviewJournal of hematology & oncology2017

XPO1 in B cell hematological malignancies: from recurrent somatic mutations to targeted therapy.

Vincent Camus, Hadjer Miloudi, Antoine Taly, Brigitte Sola, Fabrice Jardin

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
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  7. Detection ofInternational journal of molecular sciences · 2025
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  18. Nuclear transport proteins: structure, function, and disease relevance.Signal transduction and targeted therapy · 2023
    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

5 authors at 2 institutions in 1 country.

Vincent CamusNormandie Univ, INSERM U1245, UNICAEN, UNIROUEN, Caen, France.
Hadjer MiloudiNormandie Univ, INSERM U1245, UNICAEN, UNIROUEN, Caen, France.
Antoine TalyLaboratoire de Biochimie Théorique, Institut de Biologie Physico-Chimique, CNRS, Université Paris Diderot, Paris, France.
Brigitte SolaNormandie Univ, INSERM U1245, UNICAEN, UNIROUEN, Caen, France. brigitte.sola@unicaen.fr.ORCID 0000-0001-7278-9651
Fabrice JardinNormandie Univ, INSERM U1245, UNICAEN, UNIROUEN, Caen, France.
Inserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many recent publications highlight the large role of the pivotal eukaryotic nuclear export protein exportin-1 (XPO1) in the oncogenesis of several malignancies, and there is emerging evidence that XPO1 inhibition is a key target against cancer. The clinical validation of the pharmacological inhibition of XPO1 was recently achieved with the development of the selective inhibitor of nuclear export compounds, displaying an interesting anti-tumor activity in patients with massive pre-treated hematological malignancies. Recent reports have shown molecular alterations in the gene encoding XPO1 and showed a mutation hotspot (E571K) in the following two hematological malignancies with similar phenotypes and natural histories: primary mediastinal diffuse large B cell lymphoma and classical Hodgkin's lymphoma. Emerging evidence suggests that the mutant XPO1 E571K plays a role in carcinogenesis, and this variant is quantifiable in tumor and plasma cell-free DNA of patients using highly sensitive molecular biology techniques, such as digital PCR and next-generation sequencing. Therefore, it was proposed that the XPO1 E571K variant may serve as a minimal residual disease tool in this setting. To clarify and summarize the recent findings on the role of XPO1 in B cell hematological malignancies, we conducted a literature search to present the major publications establishing the landscape of XPO1 molecular alterations, their impact on the XPO1 protein, their interest as biomarkers, and investigations into the development of new XPO1-targeted therapies in B cell hematological malignancies.

Indexed as

Molecular Targeted TherapyMutationB-LymphocytesCarcinogenesisExportin 1 ProteinHematologic NeoplasmsHodgkin DiseaseHumansKaryopherinsLymphoma, Large B-Cell, DiffuseReceptors, Cytoplasmic and NuclearExportin 1 ProteinKaryopherinsReceptors, Cytoplasmic and NuclearExportinLymphomaMinimal residual diseaseTargeted therapyXPO1

Identifiers

PMID28196522
PMCPMC5307790
OpenAlexW2587923824

What OpenQuestion holds

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Registered trials

None linked

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.