白血病·淋巴瘤
白血病·淋巴瘤
백혈병·림파류
JOURNAL OF LEUKEMIA & LYMPHOMA
2009年
10期
599-602
,共4页
杨育青%马旭东%黄轶群%邹宗楷%沈洪武
楊育青%馬旭東%黃軼群%鄒宗楷%瀋洪武
양육청%마욱동%황질군%추종해%침홍무
淋巴瘤%大细胞%弥漫性%组蛋白类%甲基化%乙酰化
淋巴瘤%大細胞%瀰漫性%組蛋白類%甲基化%乙酰化
림파류%대세포%미만성%조단백류%갑기화%을선화
Lymphoma,large cell,diffuse%Histone%Methylation%Acetylation
目的 研究组蛋白H3(H3K9、H3K14)、H4(H4K5、H4K8、H4K12、H4K16)乙酰化、组蛋白H3K4、H3K9甲基化水平在弥漫性大B细胞淋巴瘤(DLBCL)细胞的表达意义及其相关性.方法 采用免疫组织化学SP法检测40例DLBCL,16例增生性淋巴结炎组织细胞中组蛋白H3、H4乙酰化水平、组蛋白H3K4、H3K9甲基化水平并进行分析和比较.结果 在DLBCL组中,乙酰化组蛋白H3、H4和甲基化组蛋白H3K4阳性高表达显著低于增生性淋巴结炎组;而甲基化组蛋白H3K9的阳性高表达则显著高于增生性淋巴结炎组(P<0.05),差异均有统计学意义.在DLBCL组,乙酰化组蛋白H3与乙酰化组蛋白H4、乙酰化组蛋白H3与甲基化组蛋白H3K4、乙酰化组蛋白H4与甲基化组蛋白H3K4的表达均有显著的相关性(P<0.01).结论 DLBCL存在组蛋白乙酰化及甲基化调控异常,可能是致病的重要因素之一.
目的 研究組蛋白H3(H3K9、H3K14)、H4(H4K5、H4K8、H4K12、H4K16)乙酰化、組蛋白H3K4、H3K9甲基化水平在瀰漫性大B細胞淋巴瘤(DLBCL)細胞的錶達意義及其相關性.方法 採用免疫組織化學SP法檢測40例DLBCL,16例增生性淋巴結炎組織細胞中組蛋白H3、H4乙酰化水平、組蛋白H3K4、H3K9甲基化水平併進行分析和比較.結果 在DLBCL組中,乙酰化組蛋白H3、H4和甲基化組蛋白H3K4暘性高錶達顯著低于增生性淋巴結炎組;而甲基化組蛋白H3K9的暘性高錶達則顯著高于增生性淋巴結炎組(P<0.05),差異均有統計學意義.在DLBCL組,乙酰化組蛋白H3與乙酰化組蛋白H4、乙酰化組蛋白H3與甲基化組蛋白H3K4、乙酰化組蛋白H4與甲基化組蛋白H3K4的錶達均有顯著的相關性(P<0.01).結論 DLBCL存在組蛋白乙酰化及甲基化調控異常,可能是緻病的重要因素之一.
목적 연구조단백H3(H3K9、H3K14)、H4(H4K5、H4K8、H4K12、H4K16)을선화、조단백H3K4、H3K9갑기화수평재미만성대B세포림파류(DLBCL)세포적표체의의급기상관성.방법 채용면역조직화학SP법검측40례DLBCL,16례증생성림파결염조직세포중조단백H3、H4을선화수평、조단백H3K4、H3K9갑기화수평병진행분석화비교.결과 재DLBCL조중,을선화조단백H3、H4화갑기화조단백H3K4양성고표체현저저우증생성림파결염조;이갑기화조단백H3K9적양성고표체칙현저고우증생성림파결염조(P<0.05),차이균유통계학의의.재DLBCL조,을선화조단백H3여을선화조단백H4、을선화조단백H3여갑기화조단백H3K4、을선화조단백H4여갑기화조단백H3K4적표체균유현저적상관성(P<0.01).결론 DLBCL존재조단백을선화급갑기화조공이상,가능시치병적중요인소지일.
Objective To investigate the expression of histone acetylated H3 and H4, methylated H3K4 and H3K9 in diffuse large B-cell lymphoma (DLBCL). Methods The expression of histone acetylated H3 and H4, methylated H3K4 and H3K9 were examined by SP immunohistochemistry technique in lymphoid tissue of 40 cases with DLBCL and 16 cases with proliferative lymphadenitis. Results The expression of histone acetylation of H3 and H4 were lower than that in proliferative lymphadenitis. Histone methylated H3K4 was lower in expression and H3K9 was in higher expression. There was a positive correlative expression between the global histone acetylation of H3 and H4, the global histone acetylation of H3, H4 and histone methylation of H3K4. Conclusion Improper modification of histone acetylations and methylations may play an important role in pathogenesis in DLBCL.