Evidence map›Paper›PMID 36497200›Full record

ArticleCells2022

RIPOR2 Expression Decreased by HPV-16 E6 and E7 Oncoproteins: An Opportunity in the Search for Prognostic Biomarkers in Cervical Cancer.

Leslie Olmedo-Nieva, J Omar Muñoz-Bello, Imelda Martínez-Ramírez, Antonio Daniel Martínez-Gutiérrez, Yunuen Ortiz-Pedraza, Claudia González-Espinosa, Vicente Madrid-Marina, Kirvis Torres-Poveda, Margarita Bahena-Roman, Marcela Lizano

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 10 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 1 country.

Leslie Olmedo-NievaUnidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología, Avenida San Fernando 22, Sección XVI, Tlalpan, Mexico City 14080, Mexico.
J Omar Muñoz-BelloUnidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología, Avenida San Fernando 22, Sección XVI, Tlalpan, Mexico City 14080, Mexico.ORCID 0000-0002-6809-0212
Imelda Martínez-RamírezUnidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología, Avenida San Fernando 22, Sección XVI, Tlalpan, Mexico City 14080, Mexico.
Antonio Daniel Martínez-GutiérrezLaboratorio de Genómica, Instituto Nacional de Cancerología, Tlalpan, Mexico City 14080, Mexico.ORCID 0000-0001-9880-5672
Yunuen Ortiz-PedrazaUnidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología, Avenida San Fernando 22, Sección XVI, Tlalpan, Mexico City 14080, Mexico.
Claudia González-EspinosaDepartamento de Farmacobiología, Centro de Investigación y de Estudios Avanzados, Unidad Sede Sur, Calzada de los Tenorios 235, Granjas Coapa, Tlalpan, Mexico City 14330, Mexico.ORCID 0000-0001-7332-3829
Vicente Madrid-MarinaCentro de Investigación en Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Cuernavaca, Morelos 62100, Mexico.
Kirvis Torres-PovedaCentro de Investigación en Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Cuernavaca, Morelos 62100, Mexico.ORCID 0000-0001-9608-9617
Margarita Bahena-RomanCentro de Investigación en Enfermedades Infecciosas, Instituto Nacional de Salud Pública, Cuernavaca, Morelos 62100, Mexico.
Marcela LizanoUnidad de Investigación Biomédica en Cáncer, Instituto Nacional de Cancerología, Avenida San Fernando 22, Sección XVI, Tlalpan, Mexico City 14080, Mexico.ORCID 0000-0002-7553-2541
Instituto Nacional de Cancerología · MXInstituto Nacional de Salud Pública · MXCentro de Investigación en Materiales Avanzados · MX

Funding

Consejo Nacional de Ciencia y Tecnología CF-2019-51488Consejo Nacional de Ciencia y Tecnología PCC 320812Consejo Nacional de Ciencia y Tecnología PRONAII Virus y Cáncer 303044National Autonomous University of Mexico PAPIIT IN200219
6 · The paper itself

Abstract

High-risk human papillomavirus (HPV) infection is the main risk factor for cervical cancer (CC) development, where the continuous expression of E6 and E7 oncoproteins maintain the malignant phenotype. In Mexico, around 70% of CC cases are diagnosed in advanced stages, impacting the survival of patients. The aim of this work was to identify biomarkers affected by HPV-16 E6 and E7 oncoproteins that impact the prognosis of CC patients. Expression profiles dependent on E6 and E7 oncoproteins, as well as their relationship with biological processes and cellular signaling pathways, were analyzed in CC cells. A comparison among expression profiles of E6- and E7-expressing cells and that from a CC cohort obtained from The Cancer Genome Atlas (TCGA) demonstrated that the expression of 13 genes impacts the overall survival (OS). A multivariate analysis revealed that the downregulated expression of RIPOR2 was strongly associated with a worse OS. RIPOR2, including its transcriptional variants, were overwhelmingly depleted in E6- and E7-expressing cells. Finally, in a Mexican cohort, it was found that in premalignant cervical lesions, RIPOR2 expression decreases as the lesions progress; meanwhile, decreased RIPOR2 expression was also associated with a worse OS in CC patients.

Indexed as

Cell Adhesion MoleculesOncogene Proteins, ViralPapillomavirus InfectionsUterine Cervical NeoplasmsFemaleHuman papillomavirus 16HumansPapillomavirus E7 ProteinsPrognosisRepressor ProteinsCell Adhesion MoleculesE6 protein, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus E7 ProteinsRepressor ProteinsRIPOR2 protein, humancervical cancerHPVHPV-16 E6 and E7prognostic biomarkerRIPOR2

Identifiers

PMID36497200
PMCPMC9740487
OpenAlexW4311674933

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.