Evidence map›Paper›PMID 26247207›Full record

ArticlePloS one2015

A Pan-GTPase Inhibitor as a Molecular Probe.

Lin Hong, Yuna Guo, Soumik BasuRay, Jacob O Agola, Elsa Romero, Denise S Simpson, Chad E Schroeder, Peter Simons, Anna Waller, Matthew Garcia and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Membrane trafficking alterations in breast cancer progression.Frontiers in cell and developmental biology · 2024
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Rab GTPases: Central Coordinators of Membrane Trafficking in Cancer.Frontiers in cell and developmental biology · 2021
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Rab5C enhances resistance to ionizing radiation in rectal cancer.Journal of molecular medicine (Berlin, Germany) · 2019
    Article
  15. Article
  16. Relevance of Rab Proteins for the Life Cycle of Hepatitis C Virus.Frontiers in cell and developmental biology · 2018
    Review
  17. Review
  18. Article
  19. Article
  20. 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

17 authors at 3 institutions in 1 country.

Lin HongDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; University of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America.
Yuna GuoDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America.
Soumik BasuRayDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America.
Jacob O AgolaDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America.
Elsa RomeroDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America.
Denise S SimpsonUniversity of Kansas Specialized Chemistry Center, Lawrence, Kansas, United States of America.
Chad E SchroederUniversity of Kansas Specialized Chemistry Center, Lawrence, Kansas, United States of America.
Peter SimonsDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; University of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America.
Anna WallerDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; University of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America.
Matthew GarciaDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; University of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America.
Mark CarterDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; University of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America.
Oleg UrsuUniversity of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America; Cancer Research and Treatment Center, University of New Mexico, Albuquerque, New Mexico, United States of America; Department of Biochemistry and Molecular Biology, University of New Mexico, Albuquerque, New Mexico, United States of America.
Kristine GouveiaDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; University of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America.
Jennifer E GoldenUniversity of Kansas Specialized Chemistry Center, Lawrence, Kansas, United States of America.
Jeffrey AubéUniversity of Kansas Specialized Chemistry Center, Lawrence, Kansas, United States of America; Department of Medicinal Chemistry, University of Kansas, Lawrence, Kansas, United States of America.
Angela Wandinger-NessDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; Cancer Research and Treatment Center, University of New Mexico, Albuquerque, New Mexico, United States of America.
Larry A SklarDepartment of Pathology, University of New Mexico, Albuquerque, New Mexico, United States of America; University of New Mexico Center for Molecular Discovery, Albuquerque, New Mexico, United States of America; Cancer Research and Treatment Center, University of New Mexico, Albuquerque, New Mexico, United States of America.
University of New Mexico · USUniversity of Kansas · USNew Mexico Cancer Center · US

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
University of Kansas Specialized Chemistry CenterU54HG005031 · NHGRI · UNIVERSITY OF KANSAS LAWRENCE · PI BLAGG, BRIAN S J · 2008 to 2013
$21.5M
Yeast Biology ConsortiumU54MH084690 · NIMH · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI TEGOS, GEORGE P · 2008 to 2013
$14.4M
Force, Conformation & Affinity in VLA-4 and LFA-1 AdhesionR01HL081062 · NHLBI · UNIVERSITY OF NEW MEXICO · PI SKLAR, LARRY A. · 2007 to 2011
$2.4M
Capitalizing on NSAID enantiomer selectivity for cancer prevention and therapy(PQR21CA170375 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI HUDSON, LAURIE G, WANDINGER-NESS, ANGELA · 2012 to 2013
$413k
HTS to identify small molecules that disrupt Rab GTPase activator and effector prR21NS066435 · NINDS · UNIVERSITY OF NEW MEXICO · PI WANDINGER-NESS, ANGELA · 2009 to 2009
$149k
HTS to Identify Specific Small Molecule Inhibitors and Activators of Ras and Ras-R03MH081231 · NIMH · UNIVERSITY OF NEW MEXICO · PI WANDINGER-NESS, ANGELA · 2007 to 2007
$25k
NCI NIH HHS P30 CA118100NCI NIH HHS R21 CA170375NCI NIH HHS R21 CA170375-01NHGRI NIH HHS U54 HG005031NHGRI NIH HHS U54HG005031NHLBI NIH HHS R01 HL081062NHLBI NIH HHS R01HL081062NIMH NIH HHS R03 MH081231NIMH NIH HHS R03 MH081231-01NIMH NIH HHS U54 MH084690NIMH NIH HHS U54MH084690NINDS NIH HHS R21 NS066435NINDS NIH HHS R21NS066435
6 · The paper itself

Abstract

Overactive GTPases have often been linked to human diseases. The available inhibitors are limited and have not progressed far in clinical trials. We report here a first-in-class small molecule pan-GTPase inhibitor discovered from a high throughput screening campaign. The compound CID1067700 inhibits multiple GTPases in biochemical, cellular protein and protein interaction, as well as cellular functional assays. In the biochemical and protein interaction assays, representative GTPases from Rho, Ras, and Rab, the three most generic subfamilies of the GTPases, were probed, while in the functional assays, physiological processes regulated by each of the three subfamilies of the GTPases were examined. The chemical functionalities essential for the activity of the compound were identified through structural derivatization. The compound is validated as a useful molecular probe upon which GTPase-targeting inhibitors with drug potentials might be developed.

Indexed as

ApoptosisCell LineCell SurvivalEnzyme InhibitorsErbB ReceptorsGTP PhosphohydrolasesHeLa CellsHeterocyclic Compounds, 2-RingHumansIntegrinsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Molecular ProbesPhosphorylationProtein Bindingrab7 GTP-Binding ProteinsCID1067700EGFR protein, humanEnzyme InhibitorsErbB ReceptorsGTP PhosphohydrolasesHeterocyclic Compounds, 2-RingIntegrinsMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Molecular Probesrab7 GTP-Binding Proteinsrab GTP-Binding Proteinsras ProteinsThiourea

Identifiers

PMID26247207
PMCPMC4527730
OpenAlexW1068061363

What OpenQuestion holds

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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.