EBV Positive Diffuse Large B Cell Lymphoma and Chronic Lymphocytic Leukemia Patients Exhibit Increased Anti-dUTPase Antibodies
Autor: | Marshall V. Williams, Maria E. Ariza |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Cancer Research Chronic lymphocytic leukemia diffuse large B cell lymphoma (DLBCL) Biology medicine.disease_cause lcsh:RC254-282 Virus Article 03 medical and health sciences 0302 clinical medicine Immune system hemic and lymphatic diseases chronic lymphocytic leukemia (CLL) medicine Epstein-Barr virus (EBV) deoxyuridine triphosphate nucleotidohydrolase (dUTPase) Toll-like receptor 2 (TLR2) Cancer medicine.disease lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens Lymphoma 030104 developmental biology Oncology 030220 oncology & carcinogenesis Cancer research biology.protein Antibody Carcinogenesis Diffuse large B-cell lymphoma |
Zdroj: | Cancers; Volume 10; Issue 5; Pages: 129 Cancers, Vol 10, Iss 5, p 129 (2018) Cancers |
ISSN: | 2072-6694 |
DOI: | 10.3390/cancers10050129 |
Popis: | The Epstein-Barr virus (EBV), which is a ubiquitous γ-herpesvirus, establishes a latent infection in more than 90% of the global adult population. EBV-associated malignancies have increased by 14.6% over the last 20 years, and account for approximately 1.5% of all cancers worldwide and 1.8% of all cancer deaths. However, the potential involvement/contribution of lytic proteins to the pathophysiology of EBV-associated cancers is not well understood. We have previously demonstrated that the EBV-deoxyuridine triphosphate nucleotidohydrolase (dUTPase) modulates innate and adaptive immune responses by engaging the Toll-Like Receptor 2 (TLR2), which leads to the modulation of downstream genes involved in oncogenesis, chronic inflammation, and in effector T-cell function. Furthermore, examination of serum samples from diffuse large B-cell lymphoma (DLBCL) and chronic lymphocytic leukemia patients revealed the presence of increased levels of anti-dUTPase antibodies in both cohorts compared to controls with the highest levels (3.67-fold increase) observed in DLBCL female cases and the lowest (2.12-fold increase) in DLBCL males. Using computer-generated algorithms, dUTPase amino acid sequence alignments, and functional studies of BLLF3 mutants, we identified a putative amino acid motif involved with TLR2 interaction. These findings suggest that the EBV-dUTPase: TLR2 interaction is a potential molecular target that could be used for developing novel therapeutics (small molecules/vaccines). |
Databáze: | OpenAIRE |
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