Evidence map›Paper›PMID 21317457›Full record

ArticleOncotarget2010

Sumoylation of vimentin354 is associated with PIAS3 inhibition of glioma cell migration.

Liming Wang, Jian Zhang, Sipra Banerjee, Laura Barnes, Venkateswara Sajja, Yiding Liu, Baochuan Guo, Yuping Du, Mukesh K Agarwal, David N Wald and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Oncotarget, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

22 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Review
  3. Cancer-Associated Dysregulation of Sumo Regulators: Proteases and Ligases.International journal of molecular sciences · 2022
    Review
  4. Review
  5. Impact of Vimentin on Regulation of Cell Signaling and Matrix Remodeling.Frontiers in cell and developmental biology · 2022
    Review
  6. Pathophysiological Role of Vimentin Intermediate Filaments in Lung Diseases.Frontiers in cell and developmental biology · 2022
    Review
  7. Article
  8. Posttranslational modifications of the cytoskeleton.Cytoskeleton (Hoboken, N.J.) · 2021
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. 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 6 institutions in 2 countries.

Liming WangSchool of Life Science, Lanzhou University, Lanzhou, P. R. China.
Jian ZhangTartis, Inc., Buffalo, USA.
Sipra BanerjeeDepartment of Cancer Biology, Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, USA.
Laura BarnesMolecular Genetics, Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, USA.
Venkateswara SajjaMolecular Genetics, Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, USA.
Yiding LiuDepartment of Chemistry, Cleveland State University, Cleveland, USA.
Baochuan GuoDepartment of Chemistry, Cleveland State University, Cleveland, USA.
Yuping DuSchool of Life Science, Lanzhou University, Lanzhou, P. R. China.
Mukesh K AgarwalInvenio Therapeutics, Inc., Cleveland, USA.
David N WaldDepartment of Pathology, Case Western Reserve University, Cleveland, USA.
Qin WangSchool of Life Science, Lanzhou University, Lanzhou, P. R. China.
Jinbo YangSchool of Life Science, Lanzhou University, Lanzhou, P. R. China.
Cleveland Clinic · USCleveland State University · USLanzhou University · CNCase Western Reserve University · USIo Therapeutics (United States) · USTartis (United States) · US

Funding

MALDI TOF TECHNOLOGY FOR MOLECULAR ANALYSIS OF CANCERR33CA081653 · NCI · CLEVELAND STATE UNIVERSITY · PI GUO, BAOCHUAN · 2002 to 2003
$567k
DEVELOPMENT OF MALDI-TOF FOR DNA SEQUENCING TECHNOLOGIESR29HG001815 · NHGRI · CLEVELAND STATE UNIVERSITY · PI GUO, BAOCHUAN · 1998 to 2002
$284k
MALDI TOF TECHNOLOGY FOR MOLECULAR ANALYSIS OF CANCERR21CA081653 · NCI · CLEVELAND STATE UNIVERSITY · PI GUO, BAOCHUAN · 2001 to 2001
$143k
NCI NIH HHS CA81653NCI NIH HHS R21 CA081653NCI NIH HHS R33 CA081653NHGRI NIH HHS HG01815
6 · The paper itself

Abstract

The invasive phenotype of glioblastoma multiforme (GBM) is a hallmark of malignant process, yet the molecular mechanisms that dictate this locally invasive behavior remain poorly understood. Over-expression of PIAS3 effectively changes cell shape and inhibits GBM cell migration. We focused on the molecular target(s) of PIAS3 stimulated sumoylation, which play an important role in the inhibition of GBM cell motility. Here we report, through the immunoprecipitation with SUMO1 antibody, followed by proteomic analysis, the identification of vimentin (vimentin354), a nuclear component in GBM cells, as the main target of sumoylation promoted by PIAS3.

Indexed as

AdenoviridaeAmino Acid SequenceBrain NeoplasmsCell Line, TumorCell MovementDown-RegulationGliomaHumansImmunoprecipitationMolecular ChaperonesMolecular Sequence DataProtein Inhibitors of Activated STATProteomicsSUMO-1 ProteinSumoylationTransfectionMolecular ChaperonesPIAS3 protein, humanProtein Inhibitors of Activated STATSUMO-1 ProteinVimentin

Identifiers

PMID21317457
PMCPMC3248133
OpenAlexW2160292692

What OpenQuestion holds

Textmetadata
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.