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المؤلفVranic, Semir
المؤلفCyprian, Farhan Sachal
المؤلفAkhtar, Saghir
المؤلفAl Moustafa, Ala-Eddin
تاريخ الإتاحة2019-04-04T08:37:31Z
تاريخ النشر2018-04-17
اسم المنشورFrontiers in Oncology
المعرّفhttp://dx.doi.org/10.3389/fonc.2018.00113
الاقتباسVranic S, Cyprian FS, Akhtar S and Al Moustafa A-E (2018) The Role of Epstein–Barr Virus in Cervical Cancer: A Brief Update. Front. Oncol. 8:113. doi: 10.3389/fonc.2018.00113
المعرّفArticle # 113
معرّف المصادر الموحدhttp://hdl.handle.net/10576/11471
الملخصEpstein-Barr virus (EBV) belongs to the group of gamma-herpes viruses and was the first recognized human oncovirus. EBV is responsible for infectious mononucleosis and multiple lymphoid and epithelial malignancies including B-cell lymphomas (Burkitt lymphoma, Hodgkin lymphoma, and post-transplant lymphoproliferative disorder), various T-cell/NK lymphoproliferative disorders, nasopharyngeal carcinoma, and gastric carcinoma, respectively. In addition, the presence of EBV has been documented in other cancers including breast, prostate, oral, and salivary gland carcinomas. The presence and role of EBV in cervical cancer and its precursor lesions (CIN) have also been described, but the results from the literature are inconsistent, and the causal role of EBV in cervical cancer pathogenesis has not been established yet. In the present review, we briefly surveyed and critically appraised the current literature on EBV in cervical cancer and its variants (lymphoepithelioma-like carcinoma) as well as its precursor lesions (CIN). In addition, we discussed the possible interactions between EBV and human papilloma virus as well as between EBV and immune checkpoint regulators (PD-L1). Though further studies are needed, the available data suggest a possible causal relationship between EBV and cervical cancer pathogenesis.
اللغةen
الناشرFrontiers Media
الموضوعEpstein–Barr virus
carcinogenesis
cervical cancer
human papilloma virus
virus
العنوانThe Role of Epstein-Barr Virus in Cervical Cancer: A Brief Update.
النوعArticle Review
رقم المجلد8
ESSN2234-943X
dc.accessType Open Access


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