2018
DOI: 10.1016/j.virusres.2018.04.009
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Conservation and polymorphism of EBV RPMS1 gene in EBV-associated tumors and healthy individuals from endemic and non-endemic nasopharyngeal carcinoma areas in China

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Cited by 13 publications
(28 citation statements)
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“…Comparison of EBV sequences from North and South China identified this SNP; the consequent Asp-to-Asn amino acid change in the RPMS1 protein was found to reduce the stability of the protein ( 10 ), although uncertainty remains about whether the RPMS1 protein is expressed in EBV-infected cells ( 11 ). A further sequence study supported this distribution of the SNP selectively in southern China ( 12 ). In our data, 95% of NPC samples from China and Hong Kong had this G155391A SNP ( Fig.…”
Section: Resultsmentioning
confidence: 54%
“…Comparison of EBV sequences from North and South China identified this SNP; the consequent Asp-to-Asn amino acid change in the RPMS1 protein was found to reduce the stability of the protein ( 10 ), although uncertainty remains about whether the RPMS1 protein is expressed in EBV-infected cells ( 11 ). A further sequence study supported this distribution of the SNP selectively in southern China ( 12 ). In our data, 95% of NPC samples from China and Hong Kong had this G155391A SNP ( Fig.…”
Section: Resultsmentioning
confidence: 54%
“…8,14,15 Of interest though, in our available data, most patients with NPC had a negative EBV result. It has been reported in numerous studies that the incidence of EBV-associated NPC appears to be related geographically 1,15,16 . The study conducted by Xu et al 1 found that the BALF2-CCT gene is a highly pathogenic EBV subtype associated with NPC and shows the strongest association with the region.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, based on this close relationship, EBV DNA or antibodies can be used as an early diagnostic tool to screen for patients with NPC. In recent years, the A157154C polymorphism of the A73 gene and the RPMS1 genotype of EBV have been identified for their susceptibility to NPC (60,61). In particular, the combination of EBV-viral capsid antigen (VCA) IgA and EBV-early antigen IgA showed better sensitivity and specificity than EBV-DNA in screening NPC high-risk family individuals (62).…”
Section: Npc Biomarkers Discovered Through Genomicsmentioning
confidence: 99%