Evidence map›Paper›PMID 29997151›Full record

ArticleMolecular cancer therapeutics2018

Therapeutic Targeting of KDM1A/LSD1 in Ewing Sarcoma with SP-2509 Engages the Endoplasmic Reticulum Stress Response.

Kathleen I Pishas, Christina D Drenberg, Cenny Taslim, Emily R Theisen, Kirsten M Johnson, Ranajeet S Saund, Ioana L Pop, Brian D Crompton, Elizabeth R Lawlor, Franck Tirode and 6 more

Abstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 66 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

16 authors at 10 institutions in 5 countries.

Kathleen I PishasCancer Therapeutics Laboratory, Discipline of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
Christina D DrenbergDivision of Pharmaceutics, College of Pharmacy, The Ohio State University, Columbus, Ohio.ORCID 0000-0001-7759-8213
Cenny TaslimCenter for Childhood Cancer and Blood Disorders, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.ORCID 0000-0003-3302-9099
Emily R TheisenCenter for Childhood Cancer and Blood Disorders, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Kirsten M JohnsonCenter for Childhood Cancer and Blood Disorders, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Ranajeet S SaundCenter for Childhood Cancer and Blood Disorders, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio.
Ioana L PopHuntsman Cancer Institute, School of Medicine, University of Utah, Salt Lake City, Utah.
Brian D CromptonDepartment of Pediatric Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.
Elizabeth R LawlorDepartment of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-2350-1540
Franck TirodeUniv Lyon, Universite Claude Bernard Lyon, Centre Leon Berard, Cancer Research Center of Lyon, Lyon, France.ORCID 0000-0003-4731-7817
Jaume MoraDepartment of Pediatric Hemato-Oncology, Hospital Sant Joan de Déu, Barcelona, Spain.ORCID 0000-0001-5023-9819
Olivier DelattreInstitut Curie, PSL Research University, Service de Genetique, Pole de Medecine Diagnostique et Theranostique, Unité de Génétique Somatique, Paris, France.
Mary C BeckerleHuntsman Cancer Institute, School of Medicine, University of Utah, Salt Lake City, Utah.ORCID 0000-0001-9176-4724
David F CallenCancer Therapeutics Laboratory, Discipline of Medicine, University of Adelaide, Adelaide, South Australia, Australia.
Sunil SharmaTGen Clinical Sciences, Applied Cancer Research and Drug Discovery, Phoenix, Arizona.
Stephen L LessnickCenter for Childhood Cancer and Blood Disorders, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio. Stephen.Lessnick@nationwidechildrens.org.
Nationwide Children's Hospital · USHuntsman Cancer Institute · USDrug Discovery Laboratory (Norway) · NOExpression Génétique Microbienne · FRHarvard University · USHospital Sant Joan de Déu Barcelona · ESThe Ohio State University · USThe University of Adelaide · AUUniversité Claude Bernard Lyon 1 · FRUniversity of Michigan · US

Funding

NCTN BIQSFP ANBL1531 (NRT)U10CA180886 · NCI · PUBLIC HEALTH INSTITUTE · PI Douglas S. Hawkins · 2014 to 2026
$390.6M
COG SDMC - Statistics CoreU10CA180899 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TODD A ALONZO · 2014 to 2026
$132.8M
Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
Support for Human Specimen Banking in NCI-Supported Cancer Clinical TrialsU24CA114766 · NCI · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI RAMIREZ MILAN, NILSA DEL CARMEN · 2005 to 2014
$14.5M
EWS/FLI AND ITS TARGETS IN EWING'S SARCOMAR01CA140394 · NCI · UNIVERSITY OF UTAH · PI LESSNICK, STEPHEN L. · 2010 to 2014
$1.5M
(PQB-2) "Driver" vs. "passenger" epigenetic events in Ewing sarcomaR01CA183776 · NCI · UNIVERSITY OF UTAH · PI LESSNICK, STEPHEN L., SHARMA, SUNIL · 2014 to 2017
$1.2M
Targeting FAK and integrin signaling in preclinical models of Ewing sarcomaK08CA188073 · NCI · DANA-FARBER CANCER INST · PI CROMPTON, BRIAN · 2015 to 2019
$886k
NCI NIH HHS K08 CA188073NCI NIH HHS P30 CA016058NCI NIH HHS P30 CA042014NCI NIH HHS R01 CA140394NCI NIH HHS R01 CA183776NCI NIH HHS U10 CA180886NCI NIH HHS U10 CA180899NCI NIH HHS U24 CA114766
6 · The paper itself

Abstract

Multi-agent chemotherapeutic regimes remain the cornerstone treatment for Ewing sarcoma, the second most common bone malignancy diagnosed in pediatric and young adolescent populations. We have reached a therapeutic ceiling with conventional cytotoxic agents, highlighting the need to adopt novel approaches that specifically target the drivers of Ewing sarcoma oncogenesis. As KDM1A/

Indexed as

AdolescentApoptosisBone NeoplasmsCell Line, TumorChildEndoplasmic Reticulum StressEnzyme InhibitorsGene Expression Regulation, NeoplasticHistone DemethylasesHumansRNA InterferenceSarcoma, EwingSignal TransductionSmall Molecule LibrariesEnzyme InhibitorsHistone DemethylasesKDM1A protein, humanSmall Molecule Libraries

Identifiers

PMID29997151
PMCPMC6201274
OpenAlexW2824417389

What OpenQuestion holds

Textmetadata
LicenceTDM
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.