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   Overexpression of activation-induced cytidine deaminase in MTX-and age-related Epstein-Barr virus-associated B-cell lymphoproliferative disorders of the head and neck  
   
نویسنده kikuchi k. ,ishige t. ,ide f. ,ito y. ,saito i. ,hoshino m. ,inoue h. ,miyazaki y. ,nozaki t. ,kojima m. ,kusama k.
منبع journal of oncology - 2015 - دوره : 2015 - شماره : 0
چکیده    Recent research has shown that activation-induced cytidine deaminase (aid) triggers somatic hypermutation and recombination,in turn contributing to lymphomagenesis. such aberrant aid expression is seen in b-cell leukemia/lymphomas,including burkitt lymphoma which is associated with c-myc translocation. moreover,epstein-barr virus (ebv) latent membrane protein-1 (lmp-1) increases genomic instability through early growth transcription response-1 (egr-1) mediated upregulation of aid in b-cell lymphoma. however,few clinicopathological studies have focused on aid expression in lymphoproliferative disorders (lpds). therefore,we conducted an immunohistochemical study to investigate the relationship between aid and lmp-1 expression in lpds (mtx-/age-related ebv-associated),including diffuse large b-cell lymphomas (dlbcls). more intense aid expression was detected in lpds (89.5%) than in dlbcls (20.0%),and the expression of lmp-1 and eber was more intense in lpds (68.4% and 94.7%) than in dlbcls (10.0% and 20.0%). furthermore,stronger egr-1 expression was found in mtx/age-ebv-lpds (83.3%) than in dlbcls (30.0%). aid expression was significantly constitutively overexpressed in lpds as compared with dlbcls. these results suggest that increased aid expression in lpds may be one of the processes involved in lymphomagenesis,thereby further increasing the survival of genetically destabilized b-cells. aid expression may be a useful indicator for differentiation between lpds and dlbcls. © 2015 kentaro kikuchi et al.
آدرس division of pathology,department of diagnostic and therapeutic sciences,meikai university school of dentistry,1-1 keyakidai,sakado, Japan, department of pathology,nihon university school of medicine,30-1 oyaguchi-kamimachi,itabashi-ku, Japan, division of pathology,department of diagnostic and therapeutic sciences,meikai university school of dentistry,1-1 keyakidai,sakado, Japan, division of diagnostic pathology,tsurumi university dental hospital,2-1-3 tsurumi,tsurumi-ku, Japan, department of pathology,tsurumi university school of dental medicine,2-1-3 tsurumi,tsurumi-ku, Japan, second division of oral and maxillofacial surgery,department of diagnostic and therapeutic sciences,meikai university school of dentistry,1-1 keyakidai,sakado, Japan, division of pathology,department of diagnostic and therapeutic sciences,meikai university school of dentistry,1-1 keyakidai,sakado, Japan, division of pathology,department of diagnostic and therapeutic sciences,meikai university school of dentistry,1-1 keyakidai,sakado, Japan, department of pharmacology,osaka dental university,8-1 kuzuhahanazono-cho,hirakata, Japan, department of anatomic and diagnostic pathology,dokkyo medical university school of medicine,880 oaza-kitakobayashi,mibu-machi,shimotsuga-gun, Japan, division of pathology,department of diagnostic and therapeutic sciences,meikai university school of dentistry,1-1 keyakidai,sakado, Japan
 
     
   
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