Evidence map›Paper›PMID 26248315›Full record

ArticlePloS one2015

SPARC Controls Melanoma Cell Plasticity through Rac1.

Edgardo Salvatierra, Mariano J Alvarez, Claudia C Leishman, Elvia Rivas Baquero, Viviana P Lutzky, H Eduardo Chuluyan, Osvaldo L Podhajcer

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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Significance of 5-International journal of molecular sciences · 2020
    Review
  5. Article
  6. Genetic variant ofArchives animal breeding · 2020
    Article
  7. Review
  8. Frontiers in cell and developmental biology · 2019
    Article
  9. Article
  10. Ectopic expression of the osteogenic master geneWorld journal of stem cells · 2018
    Article
  11. 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

7 authors at 2 institutions in 1 country.

Edgardo SalvatierraLaboratory of Molecular and Cellular Therapy, Instituto Leloir-CONICET, Buenos Aires, C1405, Argentina.
Mariano J AlvarezLaboratory of Molecular and Cellular Therapy, Instituto Leloir-CONICET, Buenos Aires, C1405, Argentina.
Claudia C LeishmanLaboratory of Molecular and Cellular Therapy, Instituto Leloir-CONICET, Buenos Aires, C1405, Argentina.
Elvia Rivas BaqueroLaboratory of Molecular and Cellular Therapy, Instituto Leloir-CONICET, Buenos Aires, C1405, Argentina.
Viviana P LutzkyLaboratory of Immunomodulators, School of Medicine, Centro de Estudios Farmacológicos y Botánicos (CEFYBO), Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET)-University of Buenos Aires, Buenos Aires, Argentina.
H Eduardo ChuluyanLaboratory of Immunomodulators, School of Medicine, Centro de Estudios Farmacológicos y Botánicos (CEFYBO), Consejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET)-University of Buenos Aires, Buenos Aires, Argentina.
Osvaldo L PodhajcerLaboratory of Molecular and Cellular Therapy, Instituto Leloir-CONICET, Buenos Aires, C1405, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARFundación Instituto Leloir · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell transition to a more aggressive mesenchymal-like phenotype is a hallmark of cancer progression that involves different steps and requires tightly regulated cell plasticity. SPARC (Secreted Protein Acidic and Rich in Cysteine) is a matricellular protein that promotes this transition in various malignant cell types, including melanoma cells. We found that suppression of SPARC expression in human melanoma cells compromised cell migration, adhesion, cytoskeleton structure, and cell size. These changes involved the Akt/mTOR pathway. Re-expression of SPARC or protein addition restored all the cell features. Suppression of SPARC expression was associated with increased Rac1-GTP levels and its membrane localization. Expression of the dominant negative mutant of Rac1 counteracted almost all the changes observed in SPARC-deficient cells. Overall, these data suggest that most of the SPARC-mediated effects occurred mainly through the blockade of Rac1 activity.

Indexed as

Cell PlasticityActin CytoskeletonCell AdhesionCell Line, TumorCell MovementDown-RegulationHumansIntegrinsMelanomaOsteonectinProto-Oncogene Proteins c-aktrac1 GTP-Binding ProteinSignal TransductionTOR Serine-Threonine KinasesIntegrinsOsteonectinProto-Oncogene Proteins c-aktrac1 GTP-Binding ProteinRAC1 protein, humanSPARC protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID26248315
PMCPMC4527691
OpenAlexW1089704793

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.