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Diffuse Large B Cell Lymphoma Shows Distinct Methylation Profiles of the Tumor Suppressor Genes among the Non-Hodgkin¡¯s Lymphomas

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À±¼±¿Á ( Yoon Sun-Och ) 
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°­°æÈÆ ( Kang Gyeong-Hoon ) 
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±è¿µ¾Æ ( Kim Young-A ) 
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±èÁöÀº ( Kim Ji-Eun ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º¸¶ó¸Åº´¿ø º´¸®°ú
ÀüÀ±°æ ( Jeon Yoon-Kyung ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç
±èö¿ì ( Kim Chul-Woo ) 
¼­¿ï´ëÇб³ ÀÇ°ú´ëÇÐ º´¸®Çб³½Ç

Abstract


Background : Aberrant methylation of CpG islands in promoter regions is one of the major mechanisms for silencing of tumor suppressor genes in various types of human cancers including non-Hodgkin¡¯¡¯ lymphomas (NHL). In this study, we investigated the aberrant promoter methylation status of known or suspected tumor suppressor genes in NHLs and compared the methylation profiles between B-cell and T/NK-cell NHLs.

Methods : 54 cases of B-cell NHLs and 16 cases of T/NK-cell NHLs were examined for the methylation status of eight genes using methylation specific PCR.

Results : CpG islands methylation was variously found in eight genes as follows; DAPK (71%), MT1G (70%), p16 (53%), CDH1 (53%), THBS1 (56%), MGMT (27.1%), COX2 (13%), and RUNX3 (11.4%). In six cases (8 %), methylation was not observed in any of these genes. Overall methylation index of B-cell NHLs (0.48) was significantly higher than that of T/NK-cell NHLs (0.32). Of eight genes tested, THBS1 and CDH1 methylations were much more prominent in diffuse large B-cell lymphomas than in T/NK-cell NHLs or other B-cell NHLs.

Conclusion : This study suggests that aberrant CpG island methylation is a frequent event in NHLs, and diffuse large B-cell lymphomas show overlapping but distinct methylation profiles.

Å°¿öµå

Lymphoma; non-Hodgkin; DNA methylation; Genes; tumor suppressor

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