臨牀消化器内科 Vol.12 No.6(6)


特集名 分子生物学と消化管
題名 MALTリンパ腫の遺伝子的検討
発刊年月 1997年 06月
著者 小野 裕之 国立がんセンター中央病院内科
著者 斉藤 大三 国立がんセンター中央病院内科
【 要旨 】 臨床における胃low-grade MALTリンパ腫の遺伝子学的検討の意義は,ひとつは確定診断に際しての補助診断であり,もう一つはH.pylori除菌効果の予測および除菌後の取扱いの判定上の補助的役割と考えられる.現時点ではMALTリンパ腫に特異的な遺伝子変化の知見は少ないが,bcl-2蛋白の発現は悪性度の増加に伴い低下し,p53はbcl-2とは逆に増加する点から悪性度の評価に,また免疫グロブリン重鎖遺伝子再構成を用いた単クローン性の証明は,除菌後の経過観察の指標となる可能性が示唆される.
Theme Molecular Biology & GI Tract
Title The Genetic Abnormality of MALT Lymphoma
Author Hiroyuki Ono National Cancer Center Hospital
Author Daizo Saito National Cancer Center Hospital
[ Summary ] In the study of immunohistochemical expression of bcl-2 and p53 using formalin-fixed, paraffin-embedded surgical specimens of MALT lymphoma, the rate of bcl-2 expression decreased as malignant potential progressed, while that of p53 showed the opposite trend and increased. Furthermore, on PCR-based analysis of biopsy specimens in our study of patients in whom H.pylori had been eradicated, the monoclonal pattern of immunoglobulin heavy chain gene rearrangement was converted to a polyclonal pattern after H.pylori eradication of which the rate was 40% (4/10). In particular, 80% of the patients with complete healing showed conversion to the polyclonal pattern. These results suggest that genetic information contributes to making the differential diagnosis between benign gastritis and gastric low-grade MALT lymphoma, as well as to assessing the most appropriate clinical management for patients after H.pylori eradication.
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