Evidence map›Paper›PMID 31578445›Full record

ArticleScientific reports2019

Human amniotic membrane conditioned medium inhibits proliferation and modulates related microRNAs expression in hepatocarcinoma cells.

Rodrigo Riedel, Antonio Pérez-Pérez, Antonio Carmona-Fernández, Mariana Jaime, Roberto Casale, José Luis Dueñas, Pilar Guadix, Víctor Sánchez-Margalet, Cecilia L Varone, Julieta L Maymó

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 24 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

10 authors at 3 institutions in 2 countries.

Rodrigo RiedelUniversidad de Buenos Aires. CONICET. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN). Ciudad Universitaria Pabellón 2, 4° piso, (1428), Buenos Aires, Argentina.
Antonio Pérez-PérezDepartamento de Bioquímica Médica y Biología Molecular, Hospital Universitario Virgen Macarena. Facultad de Medicina. Universidad de Sevilla. Avenida Sánchez Pizjuán 4 (41009), Sevilla, Spain.
Antonio Carmona-FernándezDepartamento de Bioquímica Médica y Biología Molecular, Hospital Universitario Virgen Macarena. Facultad de Medicina. Universidad de Sevilla. Avenida Sánchez Pizjuán 4 (41009), Sevilla, Spain.
Mariana JaimeHospital Nacional Profesor Alejandro Posadas, Buenos Aires, Argentina.
Roberto CasaleHospital Nacional Profesor Alejandro Posadas, Buenos Aires, Argentina.
José Luis DueñasServicio de Ginecología y Obstetricia, Hospital Universitario Virgen Macarena, Sevilla, Spain.
Pilar GuadixServicio de Ginecología y Obstetricia, Hospital Universitario Virgen Macarena, Sevilla, Spain.
Víctor Sánchez-MargaletDepartamento de Bioquímica Médica y Biología Molecular, Hospital Universitario Virgen Macarena. Facultad de Medicina. Universidad de Sevilla. Avenida Sánchez Pizjuán 4 (41009), Sevilla, Spain.ORCID http://orcid.org/0000-0001-8638-8680
Cecilia L VaroneUniversidad de Buenos Aires. CONICET. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN). Ciudad Universitaria Pabellón 2, 4° piso, (1428), Buenos Aires, Argentina.
Julieta L MaymóUniversidad de Buenos Aires. CONICET. Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales (IQUIBICEN). Ciudad Universitaria Pabellón 2, 4° piso, (1428), Buenos Aires, Argentina. jmaymo@qb.fcen.uba.ar.
Hospital Universitario Virgen Macarena · ESConsejo Nacional de Investigaciones Científicas y Técnicas · ARHospital Posadas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The placental stem cells have called the focus of attention for their therapeutic potential to treat different diseases, including cancer. There is plenty evidence about the antiproliferative, antiangiogenic and proapoptotic properties of the amniotic membrane. Liver cancer is the fifth cause of cancer in the world, with a poor prognosis and survival. Alternative treatments to radio- or chemotherapy have been searched. In this work we aimed to study the antiproliferative properties of the human amniotic membrane conditioned medium (AM-CM) in hepatocarcinoma cells. In addition, we have analyzed the regulation of pro and antiOncomiRs expression involved in hepatocarcinoma physiology. We have determined by

Indexed as

AmnionCarcinoma, HepatocellularCell Cycle CheckpointsCell ProliferationCulture Media, ConditionedCyclin D1FemaleGene Expression Regulation, NeoplasticHep G2 CellsHumansLiver NeoplasmsMicroRNAsPlacentaPregnancyProto-Oncogene Proteins c-mdm2Stem CellsCulture Media, ConditionedCyclin D1MicroRNAsProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p53

Identifiers

PMID31578445
PMCPMC6775050
OpenAlexW2978807544

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.