Evidence map›Paper›PMID 41226543›Full record

ReviewInternational journal of molecular sciences2025

DNMT Enzymes and Their Impact on Cervical Cancer: A State-of-the-Art Review.

Eric Genaro Salmerón-Bárcenas, Andrea Martínez-Zayas, Miguel Vargas-Mejía, Nicolas Villegas-Sepúlveda, Paola Briseño-Díaz, Arturo Aguilar-Rojas, Christian Johana Baños-Hernández, Francisco Israel Torres-Rojas, Ramón Antaño-Arias, Rosaura Hernández-Rivas

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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. Review
  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

10 authors.

Eric Genaro Salmerón-BárcenasDepartamento de Biomedicina Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de Mexico 07360, Mexico.
Andrea Martínez-ZayasDepartamento de Biomedicina Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de Mexico 07360, Mexico.
Miguel Vargas-MejíaDepartamento de Biomedicina Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de Mexico 07360, Mexico.ORCID 0000-0002-3031-9798
Nicolas Villegas-SepúlvedaDepartamento de Biomedicina Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de Mexico 07360, Mexico.ORCID 0000-0001-9489-2545
Paola Briseño-DíazDepartamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de Mexico 07360, Mexico.ORCID 0000-0002-4072-2433
Arturo Aguilar-RojasUnidad de Investigación Médica en Medicina Reproductiva, UMAE en Ginecología y Obstetricia No. 4, Instituto Mexicano del Seguro Social, Ciudad de Mexico 01070, Mexico.ORCID 0000-0002-8026-0552
Christian Johana Baños-HernándezInstituto de Investigación en Ciencias Biomédicas, Centro Universitario de Ciencias de la Salud, Universidad de Guadalajara, Guadalajara 44340, Mexico.ORCID 0000-0002-5424-1921
Francisco Israel Torres-RojasLaboratorio de Biomedicina Molecular, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39086, Mexico.
Ramón Antaño-AriasLaboratorio de Biomedicina Molecular, Facultad de Ciencias Químico Biológicas, Universidad Autónoma de Guerrero, Chilpancingo 39086, Mexico.ORCID 0000-0003-0486-7069
Rosaura Hernández-RivasDepartamento de Biomedicina Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Ciudad de Mexico 07360, Mexico.ORCID 0000-0002-5275-0730

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic DNA methylation is an epigenetic modification that primarily occurs at CpG sites and is associated with the transcriptional repression of genes. This process plays a crucial role in maintaining cellular homeostasis and is catalyzed by a family of enzymes known as DNA methyltransferases (DNMTs), which includes DNMT1, DNMT2, DNMT3A, DNMT3B, and DNMT3L. DNMT1 is classified as a maintenance methyltransferase, whereas DNMT3A and DNMT3B are responsible for de novo methylation. Altered expression of DNMTs has been reported in various human diseases, including cancer. Cancer remains a major global health issue, with an estimated 20 million new cases and 9.7 million deaths reported in 2022. Among women, cervical cancer (CC) ranks fourth in both incidence and mortality worldwide, with persistent infection by high-risk human papillomavirus (HR-HPV) being the primary risk factor. Several studies have demonstrated that DNMT expression and activity are upregulated in CC, suggesting their potential as diagnostic and prognostic biomarkers. HR-HPV infection appears to increase DNMT expression, thereby promoting cervical carcinogenesis through aberrant methylation and subsequent silencing of tumor-suppressor genes such as PTEN, PAX1, and TSLC1. Furthermore, DNMTs are being explored as therapeutic targets in CC. In this review, we summarize the current state of the art regarding DNMTs in cervical cancer and discuss their functional roles and potential utility as diagnostic, prognostic, and therapeutic biomarkers.

Indexed as

DNA (Cytosine-5-)-MethyltransferasesUterine Cervical NeoplasmsAnimalsBiomarkers, TumorDNA MethylationEpigenesis, GeneticFemaleGene Expression Regulation, NeoplasticHumansPapillomavirus InfectionsBiomarkers, TumorDNA (Cytosine-5-)-Methyltransferases5-mCcervical cancerDNMT1DNMT2DNMT3ADNMT3BDNMT3Lmethylation

Identifiers

PMID41226543
PMCPMC12609088

What OpenQuestion holds

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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.