Evidence map›Paper›PMID 30171047›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2018

Consecutive Day HSP90 Inhibitor Administration Improves Efficacy in Murine Models of KIT-Driven Malignancies and Canine Mast Cell Tumors.

Cheryl A London, Jaime Acquaviva, Donald L Smith, Manuel Sequeira, Luisa Shin Ogawa, Heather L Gardner, Louis Feo Bernabe, Misty D Bear, Sandra A Bechtel, David A Proia

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Second era of molecular-targeted cancer therapies in dogs.The Journal of veterinary medical science · 2023
    Review
  3. Article
  4. Article
  5. Article
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.

Cheryl A London *Departments of Veterinary Biosciences and Clinical Sciences, The Ohio State University, Columbus, Ohio. cheryl.london@tufts.edu.
Jaime Acquaviva *Synta Pharmaceuticals, Lexington, Massachusetts.
Donald L SmithSynta Pharmaceuticals, Lexington, Massachusetts.
Manuel SequeiraSynta Pharmaceuticals, Lexington, Massachusetts.
Luisa Shin OgawaSynta Pharmaceuticals, Lexington, Massachusetts.
Heather L GardnerSackler School of Graduate Biomedical Sciences, Tufts University, Boston, Massachusetts.
Louis Feo BernabeDepartments of Veterinary Biosciences and Clinical Sciences, The Ohio State University, Columbus, Ohio.
Misty D BearDepartments of Veterinary Biosciences and Clinical Sciences, The Ohio State University, Columbus, Ohio.
Sandra A BechtelDepartment of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, Missouri.ORCID 0000-0002-7773-5959
David A ProiaSynta Pharmaceuticals, Lexington, Massachusetts.
Synta Pharmaceuticals (United States) · USThe Ohio State University · USTufts University · USMissouri College · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
NCATS NIH HHS UL1 TR001070NCI NIH HHS P30 CA016058
6 · The paper itself

Abstract

purposeSTA-1474, prodrug of the heat shock protein 90 inhibitor (HSP90i) ganetespib, previously demonstrated activity in canine preclinical models of cancer; interestingly, prolonged infusions were associated with improved biologic activity. The purpose of this study was to identify the ideal treatment schedule for HSP90i in preclinical models of KIT-driven malignancies and in dogs with spontaneous mast cell tumors (MCT), where KIT is a known driver. EXPERIMENTAL

design

resultsContinuous HSP90 inhibition led to durable destabilization of client proteins

conclusionsThese data provide further evidence that prolonged HSP90i exposure improves biologic activity through sustained downregulation of client proteins.

Indexed as

Antineoplastic AgentsHSP90 Heat-Shock ProteinsLeukemia, Mast-CellProto-Oncogene Proteins c-kitAnimalsCell Line, TumorDisease Models, AnimalDogsMiceOncogenesProteolysisTreatment OutcomeTriazolesXenograft Model Antitumor AssaysAntineoplastic AgentsHSP90 Heat-Shock ProteinsProto-Oncogene Proteins c-kitSTA 9090Triazoles

Identifiers

PMID30171047
PMCPMC6696991
OpenAlexW2889442226

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.