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首页> 外文期刊>Pathology >INI1 immunohistochemical expression in glioblastoma: correlation with MGMT gene promoter methylation status and patient survival.
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INI1 immunohistochemical expression in glioblastoma: correlation with MGMT gene promoter methylation status and patient survival.

机译:胶质母细胞瘤中的INI1免疫组织化学表达:与MGMT基因启动子甲基化状态和患者生存率的相关性。

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AIMS: INI1 expression and its correlation with MGMT gene promoter methylation status and follow-up was investigated in 77 surgically removed glioblastomas then treated with radiotherapy (RT) or RT plus temozolomide (TMZ). METHODS: INI1 was determined by immunohistochemistry and MGMT by methylation-specific PCR. RESULTS: INI1 was expressed in 83.1% of cases. The median overall survival (OS) was 13.6 months in INI1+ tumours and 7.2 months in INI1- tumours. 31.3% of patients with INI1+ tumours were alive compared with 15.4% of patients with INI1- tumours. MGMT methylation was detected in 31.2% of cases. OS was significantly different between patients with methylated tumours and un-methylated tumours (p < 0.04), and between patients with RT+ TMZ and RT alone (p < 0.001). Considering both treatment and MGMT, the difference in OS was significant (p < 0.002). The difference in OS according to MGMT and INI1 was significant (p < 0.04). The longest median OS was recorded among methylated and INI1+ tumours. Among un-methylated tumours, the median OS was 11.1 months in INI1+ and 6.5 months in INI1- tumours. No patients were alive with un-methylated and INI1- tumours. CONCLUSIONS: Loss of INI1 immunohistochemical expression in glioblastoma may be indicating an underlying molecular aberration accounting for the more aggressive clinical behaviour.
机译:目的:在77例手术切除的胶质母细胞瘤中,研究了INI1的表达及其与MGMT基因启动子甲基化状态和随访的相关性,然后用放射疗法(RT)或RT加替莫唑胺(TMZ)治疗。方法:采用免疫组织化学方法测定INI1,采用甲基化特异性PCR检测MGMT。结果:INI1表达的病例为83.1%。 INI1 +肿瘤的中位总生存期(OS)为13.6个月,INI1肿瘤为7.2个月。 INI1 +肿瘤患者中31.3%存活,而INI1肿瘤患者中15.4%存活。在31.2%的病例中检测到MGMT甲基化。甲基化肿瘤患者和未甲基化肿瘤患者之间的OS显着不同(p <0.04),而RT + TMZ和单纯RT的患者之间OS(p <0.001)。同时考虑治疗和MGMT,OS差异显着(p <0.002)。根据MGMT和INI1的操作系统差异非常明显(p <0.04)。甲基化和INI1 +肿瘤的中位OS最长。在未甲基化的肿瘤中,INI1 +的中位OS为11.1个月,INI1-肿瘤的中位OS为6.5个月。没有患者未甲基化和INI1-肿瘤存活。结论:胶质母细胞瘤中INI1免疫组织化学表达的丧失可能表明潜在的分子畸变是临床行为更具侵略性的原因。

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