Evidence map›Paper›PMID 29901186›Full record

ArticleInternational journal of oncology2018

Early synergistic interactions between the HPV16‑E7 oncoprotein and 17β-oestradiol for repressing the expression of Granzyme B in a cervical cancer model.

J Antonio Munguía-Moreno, José Díaz-Chavéz, Enrique García-Villa, M Estela Albino-Sanchez, Daniel Mendoza-Villanueva, Rodolfo Ocadiz-Delgado, José Bonilla-Delgado, Armando Marín-Flores, Enoc M Cortés-Malagón, Elizabeth Alvarez-Rios and 5 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

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  5. Plants (Basel, Switzerland) · 2021
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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

15 authors at 6 institutions in 2 countries.

J Antonio Munguía-MorenoDepartment of Genetics and Molecular Biology, Centre for Research and Advanced Studies of the National Polytechnic Institute, México City 07360, México.
José Díaz-ChavézBiomedical Unit for Cancer Research, National Autonomous University of Mexico/National Institute of Cancer, México City 14080, México.
Enrique García-VillaDepartment of Genetics and Molecular Biology, Centre for Research and Advanced Studies of the National Polytechnic Institute, México City 07360, México.
M Estela Albino-SanchezDepartment of Genetics and Molecular Biology, Centre for Research and Advanced Studies of the National Polytechnic Institute, México City 07360, México.
Daniel Mendoza-VillanuevaLaboratory of Cell and Developmental Signalling, National Cancer Institute at Frederick, Frederick, MD 21702, USA.
Rodolfo Ocadiz-DelgadoDepartment of Genetics and Molecular Biology, Centre for Research and Advanced Studies of the National Polytechnic Institute, México City 07360, México.
José Bonilla-DelgadoResearch Unit of Genetics and Cancer, Juárez Hospital, México City 07760, México.
Armando Marín-FloresDepartment of Genetics and Molecular Biology, Centre for Research and Advanced Studies of the National Polytechnic Institute, México City 07360, México.
Enoc M Cortés-MalagónResearch Unit of Genetics and Cancer, Juárez Hospital, México City 07760, México.
Elizabeth Alvarez-RiosDepartment of Genetics and Molecular Biology, Centre for Research and Advanced Studies of the National Polytechnic Institute, México City 07360, México.
Alfredo Hidalgo-MirandaDepartment of Oncogenomics, National Institute of Genomic Medicine, México City 14610, México, México.
Aykut ÜrenDepartment of Oncology, Lombardi Comprehensive Cancer Centre, Georgetown University Medical Centre, Washington, DC 20057, USA.
Haydar ÇelikDepartment of Oncology, Lombardi Comprehensive Cancer Centre, Georgetown University Medical Centre, Washington, DC 20057, USA.
Paul F LambertMcArdle Laboratory for Cancer Research, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA.
Patricio GariglioDepartment of Genetics and Molecular Biology, Centre for Research and Advanced Studies of the National Polytechnic Institute, México City 07360, México.
Instituto Politécnico Nacional · MXGeorgetown University Medical Center · USFrederick National Laboratory for Cancer Research · USNational Institute of Genomic Medicine · MXUniversidad Nacional Autónoma de México · MXUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although high-risk human papillomavirus (HR‑HPV) infection has a prominent role in the aetiology of cervical cancer (CC), sex steroid hormones may also be involved in this process; however, the cooperation between oestrogen and HR‑HPV in the early stages of cervical carcinogenesis is poorly understood. Since 17β-oestradiol (E2) and the HPV type 16‑E7 oncoprotein induce CC in transgenic mice, a microarray analysis was performed in the present study to generate global gene expression profiles from 2‑month‑old FVB (non‑transgenic) and K14E7 (transgenic) mice who were left untreated or were treated for 1 month with E2. Upregulation of cancer-related genes that have not been previously reported in the context of CC, including glycerophosphodiester phosphodiesterase domain containing 3, interleukin 1 receptor type II, natriuretic peptide type C, MGAT4 family member C, lecithin-retinol acyltransferase (phosphatidylcholine-retinol-O-acyltransferase) and glucoside xylosyltransferase 2, was observed. Notably, upregulation of the serine (or cysteine) peptidase inhibitor clade B member 9 gene and downregulation of the Granzyme gene family were observed; the repression of the Granzyme B pathway may be a novel mechanism of immune evasion by cancer cells. The present results provide the basis for further studies on early biomarkers of CC risk and synergistic interactions between HR‑HPV and oestrogen.

Indexed as

AnimalsEstradiolFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGranzymesHumansMiceMice, TransgenicNatriuretic Peptide, C-TypeNeoplasms, ExperimentalOligonucleotide Array Sequence AnalysisPapillomavirus E7 ProteinsPhosphoric Diester HydrolasesReceptors, Interleukin-1 Type IIUterine Cervical NeoplasmsEstradiolglycerophosphodiester phosphodiesteraseGranzymesGzmb protein, mouseNatriuretic Peptide, C-Typeoncogene protein E7, Human papillomavirus type 16Papillomavirus E7 ProteinsPhosphoric Diester HydrolasesReceptors, Interleukin-1 Type II

Identifiers

PMID29901186
PMCPMC6017153
OpenAlexW2806785439

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.