摘要
目的:探讨245例弥漫性大B细胞淋巴瘤(DLBCL)中MYC/BCL2蛋白共表达状况及其与生发中心细胞样(GCB)及non-GCB亚型是否存在相关性。方法使用免疫组织化学方法对DLBCL石蜡标本制作的组织芯片进行MYC、BCL2、CD10、BCL6、MUM1、KI67检测,并对蛋白表达状况进行统计分析。结果245例DLBCL标本中,non-GCB患者163例(66.5%),GCB患者82例(33.5%),MYC和BCL2双阳性患者88例,占患者总数的35.9%(88/245),占non-GCB病例的41.7%(68/163),占GCB病例的24.4%(20/82),在这两种亚型表达的差异具有统计学意义(χ2=7.116,P=0.008)。结论DLBCL中MYC/BCL2蛋白共表达在non-GCB亚型比GCB亚型更多,可以按照MYC/BCL2的共表达情况,把DLBCL分成不同亚群以区别治疗和判断预后。
Objective To explore the condition of MYC/BCL2 protein coexpression in 245 patients with diffuse large B-cell lymphoma (DLBCL)and to find the correlations among MYC/BCL2 protein coexpres-sion,the germinal center B-cell-like (GCB)subtype and non-GCB subtype.Methods Paraffin-embedded lymphoma samples from 245 patients with DLBCL were studied using immunohistochemistry for MYC,BCL2, CD10,BCL6,MUM1 and KI67.And the protein expressions of them were analyzed.Results In the speci-mens of 245 patients with DLBCL,the patients with non-GCB were 163 (66.5%),and the patients with GCB were 82 (33.5%).The group of MYC/BCL2 protein coexpression comprised 35.9% (88/246)of the all patients.Non-GCB subtype group had a significantly higher frequency of MYC/BCL2 protein coexpression than the GCB subtype group (41.7%∶24.4%;χ2 =7.116,P=0.008).Conclusion The data shows that MYC/BCL2 protein coexpression occurs significantly more commonly in the non-GCB subtype.We can predict prog-nosis and choose therapeutic regimen base on the assessment for MYC and BCL2 protein expression.
出处
《国际肿瘤学杂志》
CAS
2014年第9期712-714,共3页
Journal of International Oncology
基金
基金项目:宁波市自然科学基金(2012A610200)