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1.
Virol J ; 10: 340, 2013 Nov 19.
Article in English | MEDLINE | ID: mdl-24252325

ABSTRACT

BACKGROUND: Despite the fact that the implication of human papillomavirus (HPV) in the carcinogenesis and prognosis of cervical cancer is well established, the impact of a co-infection with high risk HPV (HR-HPV) and Epstein-Barr virus (EBV) is still not fully understood. METHODS: Fifty eight randomly selected cases of squamous cell carcinomas (SCC) of the uterine cervix, 14 normal cervices specimens, 21 CIN-2/3 and 16 CIN-1 cases were examined for EBV and HPV infections. Detection of HR-HPV specific sequences was carried out by PCR amplification using consensus primers of Manos and by Digene Hybrid Capture. The presence of EBV was revealed by amplifying a 660 bp specific EBV sequence of BALF1. mRNA expression of LMP-1 in one hand and protein levels of BARF-1, LMP-1 and EBNA-1 in the other hand were assessed by RT-PCR and immunoblotting and/or immunohischemistry respectively. RESULTS: HR-HPV infection was found in patients with SCC (88%), low-grade (75%) and high grade (95%) lesions compared to only 14% of normal cervix cases. However, 69%, 12.5%, 38.1%, and 14% of SCC, CIN-1, CIN-2/3 and normal cervix tissues, respectively, were EBV infected. The highest co-infection (HR-HPV and EBV) was found in squamous cell carcinoma cases (67%). The latter cases showed 27% and 29% expression of EBV BARF-1 and LMP-1 oncogenes respectively. CONCLUSION: The high rate of HR-HPV and EBV co-infection in SCC suggests that EBV infection is incriminated in cervical cancer progression. This could be taken into account as bad prognosis in this type of cancer. However, the mode of action in dual infection in cervical oncogenesis needs further investigation.


Subject(s)
Carcinoma, Squamous Cell/virology , Coinfection/epidemiology , Epstein-Barr Virus Infections/epidemiology , Papillomavirus Infections/epidemiology , Uterine Cervical Neoplasms/virology , Algeria/epidemiology , DNA, Viral/genetics , DNA, Viral/isolation & purification , Epstein-Barr Virus Infections/complications , Female , Gene Expression Profiling , Humans , Immunoblotting , Papillomavirus Infections/complications , Polymerase Chain Reaction , Prevalence , Reverse Transcriptase Polymerase Chain Reaction
2.
Clin Cancer Res ; 13(17): 4993-5000, 2007 Sep 01.
Article in English | MEDLINE | ID: mdl-17785549

ABSTRACT

PURPOSE: EBV has been associated with nasopharyngeal carcinomas (NPC). In North Africa, the incidence is bimodal-the first peak occurring at approximately 20 years of age and the second peak occurring at approximately 50 years. Standard diagnostic tests based on immunofluorescence using anti-IgA EBV have shown that young North African patients have a negative serology compared with older patients. We are interested in two EBV-encoded oncoproteins, LMP1 and BARF1, which have thus far not been studied in terms of their potential as diagnostic markers for NPC. These two viral oncoproteins have been detected in cell culture media, so we tested whether they could be detected in the serum and saliva of patients with NPC. EXPERIMENTAL DESIGN: LMP1 and BARF1 proteins were analyzed in the sera and saliva of young patients and adult patients with NPC from North Africa and China. We then examined whether the secreted proteins had biological activity by analyzing their mitogenic activity. RESULTS: Both LMP1 and BARF1 were present in the serum and saliva from North African and Chinese patients with NPC. All young North African patients secreted both proteins, whereas 62% and 100% of adult patients secreted LMP1 and BARF1, respectively. From animal studies, the secreted LMP1 was associated with exosome-like vesicles. These secreted EBV oncoproteins showed a powerful mitogenic activity in B cells. CONCLUSION: Both proteins will be a good diagnostic marker for NPC whereas BARF1 is a particularly promising marker for all ages of patients with NPC. Their mitogenic activity suggests their implication in the oncogenic development of NPC.


Subject(s)
Nasopharyngeal Neoplasms/diagnosis , Saliva/chemistry , Viral Matrix Proteins/analysis , Viral Proteins/analysis , Adult , Animals , Antigens, CD/analysis , Cell Line, Tumor , Enzyme-Linked Immunosorbent Assay , Humans , Lymphocyte Activation , Mice , Mitogens/pharmacology , Nasopharyngeal Neoplasms/virology , Platelet Membrane Glycoproteins/analysis , Tetraspanin 30 , Viral Matrix Proteins/blood , Viral Matrix Proteins/pharmacology , Viral Proteins/blood , Viral Proteins/pharmacology
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