Evidence map›Paper›PMID 42667440›Full record

ArticleMolecular biology reports2026

Association of EBV EBNA1 C-terminal variations with severity of Invasive ductal carcinoma.

Ayesha Khattak, Sanaullah Khan, Fatima Nauman, Ijaz Ali

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Ayesha KhattakInstitute of Zoological Sciences, University of Peshawar, Peshawar, Pakistan.
Sanaullah KhanInstitute of Zoological Sciences, University of Peshawar, Peshawar, Pakistan. sanaullahkhan@uop.edu.pk.
Fatima NaumanGeneral Surgery Department, Khyber Teaching Hospital, Peshawar, Pakistan. Fatimaktk2019@gmail.com.
Ijaz AliDepartment of Math and Natural Sciences, Gulf University for Science and Technology (GUST), West Mishref, Kuwait.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer is a major cause of mortality, and Epstein-Barr virus (EBV) is considered a potential contributor to cancer development. EBV nuclear antigen 1 (EBNA1) plays a vital role in viral persistence. This study aimed to investigate the association among EBNA1 C-terminal variations and severity of invasive ductal carcinoma (IDC).

methodA total of 60 female participants, were included in this study. EBV positive biopsy samples (N = 30) were obtained from the breast cancer patients while 30 healthy females served as control. The C-terminal region of EBNA1 gene was amplified and sequenced. Statistical analysis was carried out using SPSS v25.

resultAmong the breast cancer patients, 97% had IDC and 3% had ductal carcinoma in situ. Regarding tumor grade, 3% of the patients had grade I, 63% had grade II and 33% had grade III tumors. The P-Thr (70%) and its co-infection with V-leu (30%) were observed predominantly in patients with higher grade; however, no significant association was observed. A total of 15 consensus single-nucleotide polymorphisms were observed along with six random mutations. No significant association was reported among random SNPs with breast cancer severity. Phylogenetic analysis shows that our sequences of P-Thr exhibited high similarity with reference sequence NC_009334. All control samples were EBV negative.

conclusionP-Thr was the predominant EBNA1 prototype in study population. However, no significant association was found between EBNA1 variations with breast cancer severity.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastEpstein-Barr Virus Nuclear AntigensAdultAgedEpstein-Barr Virus InfectionsFemaleHerpesvirus 4, HumanHumansMiddle AgedMutationNeoplasm GradingPhylogenyPolymorphism, Single NucleotideEBV-encoded nuclear antigen 1Epstein-Barr Virus Nuclear AntigensBreast cancerEBNA1Epstein-bar-virusmutation

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