Evidence map›Paper›PMID 30352800›Full record

ArticleMolecular cancer therapeutics2019

Therapeutic Potential of Focal Adhesion Kinase Inhibition in Small Cell Lung Cancer.

Frank Aboubakar Nana, Marylène Lecocq, Maha Zohra Ladjemi, Bruno Detry, Sébastien Dupasquier, Olivier Feron, Pierre P Massion, Yves Sibille, Charles Pilette, Sebahat Ocak

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 45 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 5 institutions in 2 countries.

Frank Aboubakar NanaInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium.
Marylène LecocqInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium.
Maha Zohra LadjemiInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium.
Bruno DetryInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium.
Sébastien DupasquierInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium.
Olivier FeronIREC, Pôle de Pharmacologie et Thérapeutique (FATH), UCL, Brussels, Belgium.
Pierre P MassionDivision of Allergy, Pulmonary, and Critical Care Medicine, Vanderbilt University Medical Center (VUMC), and Tennessee Valley Health Care Systems, Nashville, Tennessee.
Yves SibilleInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium.
Charles PiletteInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium.
Sebahat OcakInstitut de Recherche Expérimentale et Clinique (IREC), Pôle de Pneumologie, ORL et Dermatologie (PNEU), Université catholique de Louvain (UCL), Brussels, Belgium. sebahat.ocak@uclouvain.be.
UCLouvain · BECHU Dinant Godinne UCL Namur · BEAssociation Pharmaceutique Belge · BECliniques Universitaires Saint-Luc · BEVanderbilt University Medical Center · US

Funding

Phenotypic heterogeneity in small cell lung cancer.I01CX001425 · VA · VETERANS HEALTH ADMINISTRATION · PI MASSION, PIERRE P. · 2016 to 2019
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CSRD VA I01 CX001425
6 · The paper itself

Abstract

Small cell lung cancer (SCLC) has a poor prognosis. Focal adhesion kinase (FAK) is a non-receptor tyrosine kinase regulating cell proliferation, survival, migration, and invasion, which is overexpressed and/or activated in several cancers, including SCLC. We wanted to determine whether FAK contributes to SCLC aggressive behavior. We first evaluated the effect of FAK small-molecule inhibitor PF-573,228 in NCI-H82, NCI-H146, NCI-H196, and NCI-H446 SCLC cell lines. PF-573,228 (0.1-5 μmol/L) inhibited FAK activity by decreasing phospho-FAK (Tyr397), without modifying total FAK expression. PF-573,228 decreased proliferation, decreased DNA synthesis, induced cell-cycle arrest in G

Indexed as

Cell AdhesionCell CycleCell Line, TumorCell ProliferationCell SurvivalFocal Adhesion Kinase 1HumansLung NeoplasmsPhosphorylationProtein Kinase InhibitorsQuinolonesRNA, Small InterferingSmall Cell Lung CarcinomaSulfones6-(4-(3-(methylsulfonyl)benzylamino)-5-(trifluoromethyl)pyrimidin-2-ylamino)-3,4-dihydroquinolin-2(1H)-oneFocal Adhesion Kinase 1Protein Kinase InhibitorsPTK2 protein, humanQuinolonesRNA, Small InterferingSulfones

Identifiers

PMID30352800
PMCPMC6318062
OpenAlexW2895928622

What OpenQuestion holds

Textmetadata
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.