Evidence map›Paper›PMID 25147818›Full record

ArticleBioMed research international2014

Human umbilical cord perivascular cells exhibited enhanced migration capacity towards hepatocellular carcinoma in comparison with bone marrow mesenchymal stromal cells: a role for autocrine motility factor receptor.

Juan Bayo, Esteban Fiore, Jorge B Aquino, Mariana Malvicini, Manglio Rizzo, Estanislao Peixoto, Laura Alaniz, Flavia Piccioni, Marcela Bolontrade, Osvaldo Podhajcer and 2 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 22 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

12 authors at 3 institutions in 1 country.

Juan BayoLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina.ORCID 0000-0003-3999-0841
Esteban FioreLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina.ORCID 0000-0003-1059-1695
Jorge B AquinoLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina ; CONICET (Consejo Nacional de Investigaciones Científicas y Técnicas), C1033AAJ Buenos Aires, Argentina.
Mariana MalviciniLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina.
Manglio RizzoLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina.ORCID 0000-0003-2829-4701
Estanislao PeixotoLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina.ORCID 0000-0001-5226-9747
Laura AlanizLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina ; CONICET (Consejo Nacional de Investigaciones Científicas y Técnicas), C1033AAJ Buenos Aires, Argentina.ORCID 0000-0002-6070-6078
Flavia PiccioniLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina.ORCID 0000-0003-0685-9927
Marcela BolontradeCONICET (Consejo Nacional de Investigaciones Científicas y Técnicas), C1033AAJ Buenos Aires, Argentina ; Laboratorio de Terapia Molecular y Celular, Fundación Instituto Leloir, C1405BWE Buenos Aires, Argentina.
Osvaldo PodhajcerCONICET (Consejo Nacional de Investigaciones Científicas y Técnicas), C1033AAJ Buenos Aires, Argentina ; Laboratorio de Terapia Molecular y Celular, Fundación Instituto Leloir, C1405BWE Buenos Aires, Argentina.
Mariana G GarciaLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina ; CONICET (Consejo Nacional de Investigaciones Científicas y Técnicas), C1033AAJ Buenos Aires, Argentina.
Guillermo MazzoliniLaboratorio de Terapia Génica, Facultad de Ciencias Biomédicas, Universidad Austral, B1629ODT Derqui-Pilar, Buenos Aires, Argentina ; CONICET (Consejo Nacional de Investigaciones Científicas y Técnicas), C1033AAJ Buenos Aires, Argentina ; Unidad de Hígado, Hospital Universitario Austral, Universidad Austral, B1629ODT Derqui-Pilar, Argentina.
Austral University · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARFundación Instituto Leloir · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the third cause of cancer-related death worldwide. Unfortunately, the incidence and mortality associated with HCC are increasing. Therefore, new therapeutic strategies are urgently needed and the use of mesenchymal stromal cells (MSCs) as carrier of therapeutic genes is emerging as a promising option. Different sources of MSCs are being studied for cell therapy and bone marrow-derived cells are the most extensively explored; however, birth associated-tissues represent a very promising source. The aim of this work was to compare the in vitro and in vivo migration capacity between bone marrow MSCs (BM-MSCs) and human umbilical cord perivascular cells (HUCPVCs) towards HCC. We observed that HUCPVCs presented higher in vitro and in vivo migration towards factors released by HCC. The expression of autocrine motility factor (AMF) receptor, genes related with the availability of the receptor on the cell surface (caveolin-1 and -2) and metalloproteinase 3, induced by the receptor activation and important for cell migration, was increased in HUCPVCs. The chemotactic response towards recombinant AMF was increased in HUCPVCs compared to BM-MSCs, and its inhibition in the conditioned medium from HCC induced higher decrease in HUCPVC migration than in BM-MSC. Our results indicate that HUCPVCs could be a useful cellular source to deliver therapeutic genes to HCC.

Indexed as

AnimalsBone MarrowBone Marrow CellsCarcinoma, HepatocellularCaveolin 1Caveolin 2Cell LineCell Line, TumorCell MovementCulture Media, ConditionedHumansLiver NeoplasmsMaleMatrix Metalloproteinase 3Mesenchymal Stem CellsMiceCAV1 protein, humanCaveolin 1Caveolin 2Culture Media, ConditionedMatrix Metalloproteinase 3Receptors, Autocrine Motility Factor

Identifiers

PMID25147818
PMCPMC4132334
OpenAlexW2132247112

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Registered trials

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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.