Evidence map›Paper›PMID 28372578›Full record

ArticleVirology journal2017

HPV16-E2 protein modifies self-renewal and differentiation rate in progenitor cells of human immortalized keratinocytes.

Victoria Domínguez-Catzín, Alicia-María Reveles-Espinoza, Janet Sánchez-Ramos, Raúl Cruz-Cadena, Diana Lemus-Hernández, Efraín Garrido

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
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

6 authors at 2 institutions in 1 country.

Victoria Domínguez-CatzínLaboratory of Research in Cancer Molecular and Cell Biology, Department of Genetics and Molecular Biology, CINVESTAV-IPN, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, C.P. 07360, México D.F., Mexico.
Alicia-María Reveles-EspinozaLaboratory of Research in Cancer Molecular and Cell Biology, Department of Genetics and Molecular Biology, CINVESTAV-IPN, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, C.P. 07360, México D.F., Mexico.
Janet Sánchez-RamosLaboratory of Research in Cancer Molecular and Cell Biology, Department of Genetics and Molecular Biology, CINVESTAV-IPN, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, C.P. 07360, México D.F., Mexico.
Raúl Cruz-CadenaLaboratory of Research in Cancer Molecular and Cell Biology, Department of Genetics and Molecular Biology, CINVESTAV-IPN, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, C.P. 07360, México D.F., Mexico.
Diana Lemus-HernándezLaboratory of Research in Cancer Molecular and Cell Biology, Department of Genetics and Molecular Biology, CINVESTAV-IPN, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, C.P. 07360, México D.F., Mexico.
Efraín GarridoLaboratory of Research in Cancer Molecular and Cell Biology, Department of Genetics and Molecular Biology, CINVESTAV-IPN, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, C.P. 07360, México D.F., Mexico. egarrido@cinvestav.mx.
Center for Research and Advanced Studies of the National Polytechnic Institute · MXInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCervical cancer is the fourth cause of death worldwide by cancer in women and is a disease associated to persistent infection with human papillomavirus (HPV), particularly from two high-risk types HPV16 and 18. The virus initiates its replicative cycle infecting cells located in the basal layer of the epithelium, where a small population of epithelial stem cells is located performing important functions of renewal and maintenance of the tissue. Viral E2 gene is one of the first expressed after infection and plays relevant roles in the replicative cycle of the virus, modifying fundamental processes in the infected cells. Thus, the aim of the present study was to demonstrate the presence of hierarchic subpopulations in HaCaT cell line and evaluate the effect of HPV16-E2 expression, on their biological processes.

methodsHaCaT-HPV16-E2 cells were generated by transduction of HaCaT cell line with a lentiviral vector. The α6-integrin-CD71 expression profile was established by immunostaining and flow cytometric analysis. After sorting, cell subpopulations were analyzed in biological assays for self-renewal, clonogenicity and expression of stemness factors (RT-qPCR).

resultsWe identified in HaCaT cell line three different subpopulations that correspond to early differentiated cells (α6-integrin

conclusionsOur data demonstrated the presence of a small subpopulation with epithelial "progenitor cells" characteristics in the HaCaT cell line, and that HPV16-E2 expression on these cells induces early differentiation.

Indexed as

Cell DifferentiationHost-Pathogen InteractionsAntigens, CDCell LineDNA-Binding ProteinsFlow CytometryGenetic VectorsHuman papillomavirus 16HumansImmunohistochemistryIntegrin alpha6KeratinocytesLentivirusOncogene Proteins, ViralReceptors, TransferrinStem CellsAntigens, CDCD71 antigenDNA-Binding ProteinsE2 protein, Human papillomavirus type 16Integrin alpha6Oncogene Proteins, ViralReceptors, TransferrinEpithelial differentiationEpithelial progenitor cellsHaCaT cellsHPV16-E2ImmunophenotypeSelf-renewalStem cell markers

Identifiers

PMID28372578
PMCPMC5376701
OpenAlexW2604255590

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.