Evidence map›Paper›PMID 35225477›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2022

Association between Epstein-Barr Virus Gene Polymorphism and Breast Cancer Risk among Egyptian Females.

Meravt Mashaly, Doaa Ghorab, Mohamed Hegazy, Mohamed Abdelkhalek, Khaled Gaballah, Rasha Elzehery

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2022. 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
0.2field-weighted citation impact, top 48% 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, 3 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Meravt MashalyDepartment of Clinical Pathology, Clinical Microbiology Unit, Faculty of Medicine, Mansoura University, Egypt.
Doaa GhorabDepartment of Pathology, Faculty of Medicine, Mansoura University, Egypt.
Mohamed HegazySurgical Oncology, Oncology Center Mansoura University, Faculty of Medicine, Mansoura University, Egypt.
Mohamed AbdelkhalekSurgical Oncology, Oncology Center Mansoura University, Faculty of Medicine, Mansoura University, Egypt.
Khaled GaballahSurgical Oncology, Oncology Center Mansoura University, Faculty of Medicine, Mansoura University, Egypt.
Rasha ElzeheryClinical Pathology Department, Clinical Chemistry Unit, Faculty of Medicine, Mansoura University, Egypt.
Mansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpstein-Barr virus (EBV) has been implicated in the development of breast cancer (BC) since 1995. It is classified into A/B genotypes, C/D subtypes, and F/f variants according to variations in its genome.

aimTo determine the distribution difference of EBV types between BC patients and healthy controls in Egypt and to detect the association between different EBV types and BC characteristics.

methodsThree hundred and sixty-two participants (142 BC patients and 220 controls) were enrolled in this study. All participants were screened for EBV infection by determination of viral-capsid-IgG antibodies in their sera. EBNA-1 gene was detected by PCR in tumor biopsies of seropositive patients and in peripheral blood mononuclear cells of controls. A/B genotyping of EBV was performed by nested-PCR targeting the EBNA-2 gene. C/D subtypes and F/f variants were identified by Restriction fragment length polymorphism at BamHI-I W1/I1 and BamHI-F regions of EBV genome, respectively.

resultsAmong 362 participants, 300(82.9%) were EBV-seropositive, including 120/142(84.5%) of the BC patients and 180/220(81.8 %) of the controls. EBNA-1 gene was positive in 54(45%) of seropositive BC patients and in 38(21.1%) of seropositive controls. There was a significant association of EBNA-1 gene with breast cancer (OR=3.05, 95%CI=1.84-5.07). Moreover, EBNA-1 gene positivity was significantly associated with the more aggressive tumors. Genotype-A and prototype-F were predominant among patients (90.4%, 100%, respectively) as well as among controls (91.7%, 100%, respectively) with no statistical significant association with BC risk.  However, subtype-D was significantly more frequent in patients (95.6%) than in controls (64.7%) and was significantly associated with a higher BC risk as compared to subtype-C (OR=11.7, 95%CI=2.4-57.08). Subtype-D was significantly associated with higher grades tumors (100% among grade III),  with progesteron receptor-negative tumors and with HER2-positive tumors (100% for each). The combined genotypes that significantly associated with BC risk were ADF (OR=4.9) and BDF (OR=5.5).

conclusionsSubtype-D of EBV could be the only EBV type implicated in BC development among Egyptian females and associated more with poor prognosis.

Indexed as

AdultAgedBreast NeoplasmsCase-Control StudiesEgyptEpstein-Barr Virus InfectionsEpstein-Barr Virus Nuclear AntigensFemaleGenotypeHerpesvirus 4, HumanHumansLeukocytes, MononuclearMiddle AgedPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthPrognosisEBNA-2 protein, Human herpesvirus 4EBV-encoded nuclear antigen 1Epstein-Barr Virus Nuclear AntigensViral ProteinsBreastcancerEgyptEpstein-Barr VirusGenotyping

Identifiers

PMID35225477
PMCPMC9272632
OpenAlexW4214497459

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