Evidence map›Paper›PMID 30413179›Full record

ArticleStem cell research & therapy2018

Tropism of mesenchymal stem cell toward CD133

Lorena Favaro Pavon, Tatiana Tais Sibov, Andrea Vieira de Souza, Edgar Ferreira da Cruz, Suzana M F Malheiros, Francisco Romero Cabral, Jean Gabriel de Souza, Pamela Boufleur, Daniela Mara de Oliveira, Silvia Regina Caminada de Toledo and 8 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

55 citing papers in PubMed, 74 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

18 authors at 6 institutions in 1 country.

Lorena Favaro PavonDepartment of Neurosurgery, Federal University of São Paulo, São Paulo, Brazil. lorenap20111@hotmail.com.ORCID 0000-0002-9813-0705
Tatiana Tais SibovDepartment of Neurosurgery, Federal University of São Paulo, São Paulo, Brazil.
Andrea Vieira de SouzaExperimental Research Center, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Edgar Ferreira da CruzDiscipline of Nephrology, Federal University of São Paulo, São Paulo, Brazil.
Suzana M F MalheirosDepartment of Neurosurgery, Federal University of São Paulo, São Paulo, Brazil.
Francisco Romero CabralExperimental Research Center, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Jean Gabriel de SouzaLaboratory of Molecular Biology, Butantan Institute, São Paulo, Brazil.
Pamela BoufleurLaboratory of Molecular Biology, Butantan Institute, São Paulo, Brazil.
Daniela Mara de OliveiraDepartment of Genetics and Morphology, University of Brasília, Brasília, Brazil.
Silvia Regina Caminada de ToledoPediatric Oncology Institute, Grupo de Apoio ao Adolescente e à Criança com Câncer (GRAACC), Federal University of São Paulo, São Paulo, Brazil.
Luciana C MartiExperimental Research Center, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Jackeline Moraes MalheirosSão Carlos Institute of Physics, São Paulo University, São Carlos, Brazil.
Fernando F PaivaSão Carlos Institute of Physics, São Paulo University, São Carlos, Brazil.
Alberto TannúsSão Carlos Institute of Physics, São Paulo University, São Carlos, Brazil.
Sérgio Mascarenhas de OliveiraSão Carlos Institute of Physics, São Paulo University, São Carlos, Brazil.
Ana Marisa Chudzinski-TavassiLaboratory of Molecular Biology, Butantan Institute, São Paulo, Brazil.
Manoel A de Paiva NetoDepartment of Neurosurgery, Federal University of São Paulo, São Paulo, Brazil.
Sérgio CavalheiroDepartment of Neurosurgery, Federal University of São Paulo, São Paulo, Brazil.
Universidade Federal de São Paulo · BRUniversidade Federal de São Carlos · BRHospital Israelita Albert Einstein · BRInstituto Butantan · BRSupport group for adolescents and children with cancer · BRUniversidade de Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have demonstrated remarkable tropism of mesenchymal stem cells (MSCs) toward malignant gliomas, making these cells a potential vehicle for delivery of therapeutic agents to disseminated glioblastoma (GBM) cells. However, the potential contribution of MSCs to tumor progression is a matter of concern. It has been suggested that CD133 METHODS/

resultsWe found that isolated and cultured MSCs (human umbilical cord blood MSCs) express CCR2 and CXCR4, the respective receptors for MCP-1/CCL2 and SDF-1/CXCL12, and demonstrated, in vitro, that MCP-1/CCL2 and SDF-1/CXC12, secreted by CD133

conclusionsTherefore, in this study, we validated the chemotactic effect of MCP-1/CCL2 and SDF-1/CXCL12 in mediating the migration of MSCs toward CD133

Indexed as

TropismAC133 AntigenAnimalsBrain NeoplasmsCarcinogenesisCell Migration AssaysCell ProliferationCell SeparationChemokinesGlioblastomaHumansImmunophenotypingMaleMesenchymal Stem CellsModels, BiologicalNeoplastic Stem CellsAC133 AntigenChemokinesReceptors, ChemokineCD133+ cellsChemokinesExosomesExperimental modelMSCsTropism

Identifiers

PMID30413179
PMCPMC6234773
OpenAlexW2899807358

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.