Evidence map›Paper›PMID 24946002›Full record

ArticleBritish journal of cancer2014

KPT-330 has antitumour activity against non-small cell lung cancer.

H Sun, N Hattori, W Chien, Q Sun, M Sudo, G L E-Ling, L Ding, S L Lim, S Shacham, M Kauffman and 2 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 72 citations in OpenAlex.

  1. Trial
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  8. Michael Acceptors as Anti-Cancer Compounds: Coincidence or Causality?International journal of molecular sciences · 2024
    Review
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  14. 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

12 authors at 4 institutions in 3 countries.

H SunDepartment of Hematology and Oncology, Cedars-Sinai Medical Center, Los Angeles, CA, USA.
N HattoriCancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
W ChienCancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
Q SunCancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
M SudoCancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
G L E-LingCancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
L DingCancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
S L LimCancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
S ShachamKaryopharm Therapeutics, Boston, MA 01760, USA.
M KauffmanKaryopharm Therapeutics, Boston, MA 01760, USA.
T NakamakiDivision of Hematology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
H P Koeffler1] Department of Hematology and Oncology, Cedars-Sinai Medical Center, Los Angeles, CA, USA [2] Cancer Science Institute of Singapore, National Cancer Institute, NUS, Singapore, Singapore.
National University Cancer Institute, Singapore · SGKaryopharm Therapeutics (United States) · USCedars-Sinai Medical Center · USShowa University · JP

Funding

REGULATION OF HEMATOPOIETIC CYTOKINESR01CA026038 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KOEFFLER, HAROLD PHILLIP · 1985 to 2013
$4.7M
NCI NIH HHS R01 CA026038NCI NIH HHS R01CA026038-35
6 · The paper itself

Abstract

backgroundWe investigated the biologic and pharmacologic activities of a chromosome region maintenance 1 (CRM1) inhibitor against human non-small cell lung cancer (NSCLC) cells both in vitro and in vivo.

methodsThe in vitro and in vivo effects of a novel CRM1 inhibitor (KPT-330) for a large number of anticancer parameters were evaluated using a large panel of 11 NSCLC cell lines containing different key driver mutations. Mice bearing human NSCLC xenografts were treated with KPT-330, and tumour growth was assessed.

resultsKPT-330 inhibited proliferation and induced cell cycle arrest and apoptosis-related proteins in 11 NSCLC cells lines. Moreover, the combination of KPT-330 with cisplatin synergistically enhanced the cell kill of the NSCLC cells in vitro. Human NSCLC tumours growing in immunodeficient mice were markedly inhibited by KPT-330. Also, KPT-330 was effective even against NSCLC cells with a transforming mutation of either exon 20 of EGFR, TP53, phosphatase and tensin homologue, RAS or PIK3CA, suggesting the drug might be effective against a variety of lung cancers irrespective of their driver mutation.

conclusionsOur results support clinical testing of KPT-330 as a novel therapeutic strategy for NSCLC.

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsApoptosisCarcinoma, Non-Small-Cell LungCell Growth ProcessesCell Line, TumorCisplatinExportin 1 ProteinG1 PhaseGenes, p53HumansHydrazinesKaryopherinsLung NeoplasmsMaleAntineoplastic AgentsCisplatinExportin 1 ProteinHydrazinesKaryopherinsReceptors, Cytoplasmic and NuclearselinexorTriazoles

Identifiers

PMID24946002
PMCPMC4102938
OpenAlexW2011275571

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.