Evidence map›Paper›PMID 37434588›Full record

ArticleBreast cancer (Dove Medical Press)2023

Promoter Methylation-Regulated Differentially Expressed Genes in Breast Cancer.

Samar Sindi, Norah Hamdi, Sabah Hassan, Magdah Ganash, Mona Alharbi, Najla Alburae, Sheren Azhari, Shadi Alkhayyat, Ayman Linjawi, Heba Alkhatabi and 5 more

Open access · goldAbstract read
In one paragraph

Article in Breast cancer (Dove Medical Press), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Cancers · 2024
    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

15 authors at 2 institutions in 1 country.

Samar Sindi *Department of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Norah Hamdi *Department of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Sabah HassanDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Magdah GanashDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-3709-0487
Mona AlharbiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Najla AlburaeDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Sheren AzhariDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Shadi AlkhayyatDepartment of Internal Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Ayman LinjawiMedical Reference Clinics, Jeddah, Saudi Arabia.
Heba AlkhatabiHematology Research Unit (HRU), King Fahad Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.
Aisha ElaimiDepartment of Medical Laboratory Science, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-3214-4714
Ghadeer AlrefaeiDepartment of Biology, University of Jeddah, Jeddah, Saudi Arabia.
Nouf AlsubhiBiological Sciences Department, College of Science & Arts, King Abdulaziz University, Rabigh, Saudi Arabia.
Aziza AlrafiahDepartment of Medical Laboratory Science, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-0978-5775
Safiah AlhazmiDepartment of Biological Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.ORCID 0000-0003-0755-4498
King Abdulaziz University · SAUniversity of Jeddah · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Breast cancer is one of the most common malignancies among women. Recent studies revealed that differentially methylated regions (DMRs) are implicated in regulating gene expression. The goal of this research was to determine which genes and pathways are dysregulated in breast cancer when their promoters are methylated in an abnormal way, leading to differential expression. Whole-genome bisulfite sequencing was applied to analyze DMRs for eight peripheral blood samples collected from five Saudi females diagnosed with stages I and II of breast cancer aligned with three normal females. Three of those patients and three normal samples were used to determine differentially expressed genes (DEG) using Illumina platform NovaSeq PE150. Results: Based on ontology (GO) and KEGG pathways, the analysis indicated that DMGs and DEG are closely related to associated processes, such as ubiquitin-protein transferase activity, ubiquitin-mediated proteolysis, and oxidative phosphorylation. The findings indicated a potentially significant association between global hypomethylation and breast cancer in Saudi patients. Our results revealed 81 differentially promoter-methylated and expressed genes. The most significant differentially methylated and expressed genes found in gene ontology (GO) are pumilio RNA binding family member 1 ( Conclusion: The essential outcomes of this study suggested that aberrant hypermethylation at crucial genes that have significant parts in the molecular pathways of breast cancer could be used as a potential prognostic biomarker for breast cancer.

Indexed as

biomarkerbreast cancerdifferentially expressed genedifferentially methylated regionsDNA methylationwhole-genome bisulfite sequencing

Identifiers

PMID37434588
PMCPMC10332364
OpenAlexW4383368829

What OpenQuestion holds

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LicenceCC BY-NC
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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.