Evidence map›Paper›PMID 41983230›Full record

ArticleInternational journal of breast cancer2026

MMTV Virus Detection, Survival Analysis, and Prognostic Relevance of Six Tumor Genes in Patients With Breast Cancer.

Saad Alamri, Maaweya Awadalla, Rahaf A Henawi, Ghaida Al-Hazzaa, Zahra Alkhunaizy, Soha Alzorgi, Nouf Alqahtani, Alyaa S Abdel Halim, Mohamed A M Ali, Mansour I Almansour and 1 more

Abstract read
In one paragraph

Article in International journal of breast cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Saad AlamriResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.
Maaweya AwadallaResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.ORCID https://orcid.org/0000-0002-1270-2216
Rahaf A HenawiResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.
Ghaida Al-HazzaaResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.
Zahra AlkhunaizyPathology and Clinical Laboratory Medicine Administration, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.
Soha AlzorgiAnesthesiology and Operating Room Administration, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.
Nouf AlqahtaniComprehensive Cancer Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.
Alyaa S Abdel HalimDepartment of Biochemistry, Faculty of Science, Ain Shams University, Cairo, Egypt, asu.edu.eg.
Mohamed A M AliDepartment of Biology, College of Science, Imam Mohammad Ibn Saud Islamic University (IMSIU), Riyadh, Saudi Arabia, imamu.edu.sa.ORCID https://orcid.org/0000-0001-8217-0262
Mansour I AlmansourDepartment of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia, ksu.edu.sa.
Bandar AlosaimiResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh, Saudi Arabia, kfmc.med.sa.ORCID https://orcid.org/0000-0003-4719-2655

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objectives: Breast cancer (BC) remains the most frequently diagnosed malignancy among women worldwide and represents a significant global health burden. The genes associated with tumor suppression (p53, BRCA1, and BRCA2), telomere length maintenance (TERT), DNA damage response (FGFR2), and DNA repair (CHD1) are recognized for their intricate function in tumor genesis and progression. However, the prognostic significance of these genes in BC remains an area of research interest. This study aimed to examine the potential association between the presence of the MMTV and the expression patterns of these six genes with patient prognosis and survival outcomes in BC. Methods: This study includes 125 formalin-fixed, paraffin-embedded (FFPE) tissue specimens taken from BC patients, in addition to 25 tissue samples of benign breast lesions were incorporated as controls. The mRNA expression levels of six genes, namely p53, BRCA1, BRCA2, TERT, FGFR2, and CHD1, were quantified in FFPE tissue samples using quantitative polymerase chain reaction (qPCR). The correlation between gene expression and prognostic characteristics and the probability of recurrence-free survival (RFS) and overall survival (OS) were assessed. Results: The results do not indicate an association between MMTV and BC, as the virus was not detected in any of the tissue samples analyzed. We observed a significant differential expression in five of the six studied genes between BC and noncancerous breast tissue, with significant downregulation of BRCA1, BRCA2, CHD1, and TERT, significant upregulation of p53, and unchanged levels of FGFR2. Among BC patients, p53 and BRCA1 expression levels emerged as significant prognostic factors for both RFS (32 vs. 24 months; 34 vs. 26 months) and OS (28.5 vs. 24 months; 31 vs. 28 months), respectively. Kaplan-Meier survival analysis of p53 expression displayed a trend favoring low expression for better survival and showing relatively stable RFS and OS survival curves of p53 until 43 and 54 months of the follow-up period, respectively. Conclusions: When comparing cancer to noncancer patients, only p53 and BRCA1 expression levels emerged as significant prognostic factors for both RFS and OS in the entire cohort, with p53 displaying a trend favoring low expression for better survival. Although gene expression data provided a prognostic value, future studies should aim at integrating multiomics data and evaluating biomarkers in a broader clinical context to improve the accuracy of prognostic models and guide personalized treatment strategies.

Indexed as

breast cancerDNA repairKaplan–Meier survival analysismouse mammary tumor virus (MMTV)telomere lengthtumor suppressor genes

Identifiers

PMID41983230
PMCPMC13071179

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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.