Evidence map›Paper›PMID 26975392›Full record

ArticleBMC cancer2016

Relevance of miR-21 in regulation of tumor suppressor gene PTEN in human cervical cancer cells.

Oscar Peralta-Zaragoza, Jessica Deas, Angélica Meneses-Acosta, Faustino De la O-Gómez, Gloria Fernández-Tilapa, Claudia Gómez-Cerón, Odelia Benítez-Boijseauneau, Ana Burguete-García, Kirvis Torres-Poveda, Victor Hugo Bermúdez-Morales and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 101 citations in OpenAlex.

  1. Pooled it
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  8. New evidence for miRNA testing in head and neck squamous cell cancer patients.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Observational
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  15. Progress in the effect of microRNA-21 on diseases via autophagy.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2022
    Article
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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

14 authors at 5 institutions in 1 country.

Oscar Peralta-ZaragozaDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico. operalta@insp.mx.
Jessica DeasDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Angélica Meneses-AcostaPharmaceutical Biotechnology Laboratory, Faculty of Pharmacy, Autonomous University of Morelos State, Avenida Universidad No. 1001, Cuernavaca, Morelos, México, 62010, Mexico.
Faustino De la O-GómezDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Gloria Fernández-TilapaClinical Research Laboratory, Academic Unit of Biological Chemical Sciences, Guerrero Autonomous University, Avenida Lázaro Cárdenas S/N, Col. Haciendita, Chilpancingo, Guerrero, México, 39070, Mexico.
Claudia Gómez-CerónDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Odelia Benítez-BoijseauneauDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Ana Burguete-GarcíaDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Kirvis Torres-PovedaDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Victor Hugo Bermúdez-MoralesDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Vicente Madrid-MarinaDirection of Chronic Infections and Cancer, Research Center in Infection Diseases, National Institute of Public Health, Av. Universidad No. 655, Cerrada los Pinos y Caminera, Colonia Santa María Ahuacatitlán, Cuernavaca, Morelos, México, 62100, Mexico.
Mauricio Rodríguez-DorantesNational Institute of Genomic Medicine, Periférico Sur No. 4809, Col. Arenal Tepepan, Delegación Tlalpan, México, D.F., C.P. 14610, Mexico.
Alfredo Hidalgo-MirandaNational Institute of Genomic Medicine, Periférico Sur No. 4809, Col. Arenal Tepepan, Delegación Tlalpan, México, D.F., C.P. 14610, Mexico.
Carlos Pérez-PlasenciaOncogenomics Laboratory, National Cancer Institute of Mexico, Tlalpan, Av. San Fernando No. 22, Colonia Sección XVI, Delegación Tlalpan, Distrito Federal, México, 14080, Mexico.
Instituto Nacional de Salud Pública · MXNational Institute of Genomic Medicine · MXUniversidad Autónoma de Guerrero · MXUniversidad Autónoma del Estado de Morelos · MXUniversidad Latina de América · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExpression of the microRNA miR-21 has been found to be altered in almost all types of cancers and it has been classified as an oncogenic microRNA or oncomir. Due to the critical functions of its target proteins in various signaling pathways, miR-21 is an attractive target for genetic and pharmacological modulation in various cancers. Cervical cancer is the second most common cause of death from cancer in women worldwide and persistent HPV infection is the main etiologic agent. This malignancy merits special attention for the development of new treatment strategies. In the present study we analyze the role of miR-21 in cervical cancer cells.

methodsTo identify the downstream cellular target genes of upstream miR-21, we silenced endogenous miR-21 expression in a cervical intraepithelial neoplasia-derived cell lines using siRNAs. The effect of miR-21 on gene expression was assessed in cervical cancer cells transfected with the siRNA expression plasmid pSIMIR21. We identified the tumor suppressor gene PTEN as a target of miR-21 and determined the mechanism of its regulation throughout reporter construct plasmids. Using this model, we analyzed the expression of miR-21 and PTEN as well as functional effects such as autophagy and apoptosis induction.

resultsIn SiHa cells, there was an inverse correlation between miR-21 expression and PTEN mRNA level as well as PTEN protein expression in cervical cancer cells. Transfection with the pSIMIR21 plasmid increased luciferase reporter activity in construct plasmids containing the PTEN-3'-UTR microRNA response elements MRE21-1 and MRE21-2. The role of miR-21 in cell proliferation was also analyzed in SiHa and HeLa cells transfected with the pSIMIR21 plasmid, and tumor cells exhibited markedly reduced cell proliferation along with autophagy and apoptosis induction.

conclusionsWe conclude that miR-21 post-transcriptionally down-regulates the expression of PTEN to promote cell proliferation and cervical cancer cell survival. Therefore, it may be a potential therapeutic target in gene therapy for cervical cancer.

Indexed as

ApoptosisCell ProliferationFemaleGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHeLa CellsHumansMicroRNAsPTEN PhosphohydrolaseRNA, Small InterferingUterine Cervical NeoplasmsMicroRNAsMIRN21 microRNA, humanPTEN PhosphohydrolasePTEN protein, humanRNA, Small InterferingCervical cancermicroRNAsmiR-21PTENsiRNAs

Identifiers

PMID26975392
PMCPMC4791868
OpenAlexW2301864188

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.