Evidence map›Paper›PMID 36722323›Full record

ArticleJournal of cellular and molecular medicine2023

Protein biomarkers for response to XPO1 inhibition in haematologic malignancies.

Tulasigeri M Totiger, Sana Chaudhry, Elgilda Musi, Jumana Afaghani, Skye Montoya, Frank Owusu-Ansah, Stanley Lee, Gary Schwartz, Virginia Klimek, Justin Taylor

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 4 institutions in 1 country.

Tulasigeri M TotigerSylvester Comprehensive Cancer Center at the University of Miami Miller School of Medicine, Miami, Florida, USA.
Sana ChaudhrySylvester Comprehensive Cancer Center at the University of Miami Miller School of Medicine, Miami, Florida, USA.
Elgilda MusiColumbia University School of Medicine, New York, New York, USA.
Jumana AfaghaniSylvester Comprehensive Cancer Center at the University of Miami Miller School of Medicine, Miami, Florida, USA.
Skye MontoyaSylvester Comprehensive Cancer Center at the University of Miami Miller School of Medicine, Miami, Florida, USA.
Frank Owusu-AnsahMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Stanley LeeFred Hutchinson Cancer Center, Seattle, Washington, USA.
Gary SchwartzColumbia University School of Medicine, New York, New York, USA.
Virginia KlimekMemorial Sloan Kettering Cancer Center, New York, New York, USA.
Justin TaylorSylvester Comprehensive Cancer Center at the University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID 0000-0003-4407-6325
University of Miami · USColumbia University · USMemorial Sloan Kettering Cancer Center · USFred Hutch Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Defining the Biological and Mechanistic Implications of XPO1 Mutations in Hematologic MalignanciesK08CA230319 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI TAYLOR, JUSTIN · 2018 to 2023
$1.2M
NCI NIH HHS K08 CA230319NCI NIH HHS K08CA230319NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

XPO1 (Exportin-1) is the nuclear export protein responsible for the normal shuttling of several proteins and RNA species between the nucleocytoplasmic compartment of eukaryotic cells. XPO1 recognizes the nuclear export signal (NES) of its cargo proteins to facilitate its export. Alterations of nuclear export have been shown to play a role in oncogenesis in several types of solid tumour and haematologic cancers. Over more than a decade, there has been substantial progress in targeting nuclear export in cancer using selective XPO1 inhibitors. This has resulted in recent approval for the first-in-class drug selinexor for use in relapsed, refractory multiple myeloma and diffuse large B-cell lymphoma (DLBCL). Despite these successes, not all patients respond effectively to XPO1 inhibition and there has been lack of biomarkers for response to XPO1 inhibitors in the clinic. Using haematologic malignancy cell lines and samples from patients with myelodysplastic neoplasms treated with selinexor, we have identified XPO1, NF-κB(p65), MCL-1 and p53 protein levels as protein markers of response to XPO1 inhibitor therapy. These markers could lead to the identification of response upon XPO1 inhibition for more accurate decision-making in the personalized treatment of cancer patients undergoing treatment with selinexor.

Indexed as

Hematologic NeoplasmsMultiple MyelomaActive Transport, Cell NucleusHumansHydrazinesKaryopherinsTriazolesHydrazinesKaryopherinsselinexorTriazolesexportin-1haematologic malignanciesnuclear exportprotein biomarkerprotein cargoesXPO1 inhibitionXPO1 mutation

Identifiers

PMID36722323
PMCPMC9930413
OpenAlexW4318753918

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.