Evidence map›Paper›PMID 37548362›Full record

ArticleMolecular genetics & genomic medicine2023

Promoter hypermethylation of RARB and GSTP1 genes in plasma cell-free DNA as breast cancer biomarkers in Peruvian women.

Pierina Danos, Stefano Giannoni-Luza, Alexis Germán Murillo Carrasco, Oscar Acosta, Maria Luisa Guevara-Fujita, José Manuel Cotrina Concha, Henry Guerra Miller, Joseph Pinto Oblitas, Alfredo Aguilar Cartagena, Jhajaira M Araujo and 2 more

Open access · goldAbstract readControlled Clinical Trial
In one paragraph

Article in Molecular genetics & genomic medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Glutathione-Dependent Pathways in Cancer Cells.International journal of molecular sciences · 2024
    Review
  5. Article
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

12 authors at 4 institutions in 1 country.

Pierina DanosCentro de Genética y Biología Molecular, Universidad de San Martín de Porres, Lima, Peru.
Stefano Giannoni-LuzaCentro de Genética y Biología Molecular, Universidad de San Martín de Porres, Lima, Peru.
Alexis Germán Murillo CarrascoCentro de Genética y Biología Molecular, Universidad de San Martín de Porres, Lima, Peru.ORCID 0000-0002-7372-2608
Oscar AcostaFacultad de Medicina Humana, Universidad de San Martín de Porres, Chiclayo, Peru.
Maria Luisa Guevara-FujitaCentro de Genética y Biología Molecular, Universidad de San Martín de Porres, Lima, Peru.
José Manuel Cotrina ConchaInstituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru.
Henry Guerra MillerInstituto Nacional de Enfermedades Neoplásicas (INEN), Lima, Peru.
Joseph Pinto OblitasOncosalud-Auna, Lima, Peru.
Alfredo Aguilar CartagenaOncosalud-Auna, Lima, Peru.
Jhajaira M AraujoOncosalud-Auna, Lima, Peru.
Ricardo FujitaCentro de Genética y Biología Molecular, Universidad de San Martín de Porres, Lima, Peru.ORCID 0000-0002-9617-5109
José Luis Buleje SonoCentro de Genética y Biología Molecular, Universidad de San Martín de Porres, Lima, Peru.ORCID 0000-0002-2834-8290
Universidad de San Martín de Porres · PEEsSALUD · PEInstituto Nacional de Enfermedades Neoplásicas · PENational University of San Marcos · PE

Funding

Oncosalud-AUNAOrigenetica SACPrograma Nacional de Innovación para la Competitividad y Productividad - Innóvate Perú 138-PNICP-PIAP-2015Universidad de San Martín de Porres, Facultad de Medicina Humana Project E10012016038
6 · The paper itself

Abstract

backgroundPromoter hypermethylation is one of the enabling mechanisms of hallmarks of cancer. Tumor suppressor genes like RARB and GSTP1 have been reported as hypermethylated in breast cancer tumors compared with normal tissues in several populations. This case-control study aimed to determine the association between the promoter methylation ratio (PMR) of RARB and GSTP1 genes (separately and as a group) with breast cancer and its clinical-pathological variables in Peruvian patients, using a liquid biopsy approach.

methodsA total of 58 breast cancer patients and 58 healthy controls, matched by age, participated in the study. We exacted cell-free DNA (cfDNA) from blood plasma and converted it by bisulfite salts. Methylight PCR was performed to obtain the PMR value of the studied genes. We determined the association between PMR and breast cancer, in addition to other clinicopathological variables. The sensitivity and specificity of the PMR of these genes were obtained.

resultsA significant association was not found between breast cancer and the RARB PMR (OR = 1.90; 95% CI [0.62-6.18]; p = 0.210) or the GSTP1 PMR (OR = 6.57; 95% CI [0.75-307.66]; p = 0.114). The combination of the RARB + GSTP1 PMR was associated with breast cancer (OR = 2.81; 95% CI [1.02-8.22]; p = 0.026), controls under 50 years old (p = 0.048), patients older than 50 (p = 0.007), and postmenopausal (p = 0.034). The PMR of both genes showed a specificity of 86.21% and a sensitivity of 31.03%.

conclusionPromoter hypermethylation of RARB + GSTP1 genes is associated with breast cancer, older age, and postmenopausal Peruvian patients. The methylated promoter of the RARB + GSTP1 genes needs further validation to be used as a biomarker for liquid biopsy and as a recommendation criterion for additional tests in asymptomatic women younger than 50 years.

Indexed as

Breast NeoplasmsBiomarkers, TumorBreastCase-Control StudiesDNA MethylationFemaleGlutathione S-Transferase piHumansMiddle AgedPeruReceptors, Retinoic AcidBiomarkers, TumorGlutathione S-Transferase piGSTP1 protein, humanReceptors, Retinoic Acidretinoic acid receptor betabreast cancercfDNAGSTP1liquid biopsyMethylightPMRRARB

Identifiers

PMID37548362
PMCPMC10724513
OpenAlexW4385616853

What OpenQuestion holds

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Registered trials

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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.