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Akt/蛋白激酶B过表达作为成人弥漫性星形细胞瘤的准确预后标志物。

Akt/protein kinase B overexpression as an accurate prognostic marker in adult diffuse astrocytoma.

作者信息

Matsutani Tomoo, Nagai Yuichiro, Mine Seiichiro, Murai Hisayuki, Saeki Naokatsu, Iwadate Yasuo

机构信息

Department of Neurological Surgery, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba City, Chiba, 260-8670, Japan.

出版信息

Acta Neurochir (Wien). 2009 Mar;151(3):263-8; discussion 268. doi: 10.1007/s00701-009-0199-3. Epub 2009 Feb 25.

Abstract

BACKGROUND

Akt/Protein kinase B (PKB) is a common downstream molecule of Ras signaling essential for cell survival. In an attempt to find a novel prognostic marker of diffuse astrocytoma, we performed an immunohistochemical analysis of Akt/PKB with regard to patient survival and regrowth patterns.

METHODS

Twenty-four adult patients with diffuse astrocytoma were similarly managed without early post-operative radiotherapy and followed up for a median period of 7.5 years. They were analysed by immunohistochemistry for Akt/PKB expression as well as p53 protein accumulation, epidermal growth factor receptor (EGFR) expression, and MIB-1 labeling index. The prognostic significance of each molecular covariate was tested by multivariate analysis using Cox's proportional hazard model including age, performance status, and extent of surgical resection.

FINDINGS

Akt/PKB overexpression significantly correlated with both shorter overall survival (OS) and progression-free survival (PFS) (p = 0.0110). All the Akt/PKB-positive patients with post-operative residual tumours experienced tumour recurrences, whereas only a small fraction of the Akt/PKB-negative individuals had recurrences (p = 0.0070). Invasive recurrence into surrounding brain occurred only in the Akt/PKB-overexpressed tumours. In contrast, MIB-1 labeling index correlated only with OS, while p53 protein accumulation correlated only with PFS. The Cox's proportional hazard model identified Akt/PKB overexpression as a significant prognostic factor for shorter PFS (p = 0.0117).

CONCLUSION

These results show that Akt/PKB overexpression would be suggestive of malignant progression and invasive regrowth of diffuse astrocytoma, and it can serve as a novel prognostic marker for this tumour.

摘要

背景

Akt/蛋白激酶B(PKB)是Ras信号通路的常见下游分子,对细胞存活至关重要。为了寻找弥漫性星形细胞瘤的新型预后标志物,我们对Akt/PKB进行了免疫组化分析,以研究患者的生存情况和肿瘤复发模式。

方法

24例成年弥漫性星形细胞瘤患者在术后未早期进行放疗,采用相似的治疗方案,并进行了中位时间为7.5年的随访。通过免疫组化分析他们的Akt/PKB表达、p53蛋白积聚、表皮生长因子受体(EGFR)表达和MIB-1标记指数。使用Cox比例风险模型进行多因素分析,以检验每个分子协变量的预后意义,该模型包括年龄、体能状态和手术切除范围。

结果

Akt/PKB过表达与较短的总生存期(OS)和无进展生存期(PFS)均显著相关(p = 0.0110)。所有术后有残留肿瘤的Akt/PKB阳性患者均出现肿瘤复发,而只有一小部分Akt/PKB阴性患者复发(p = 0.0070)。仅在Akt/PKB过表达的肿瘤中出现向周围脑组织的浸润性复发。相比之下,MIB-1标记指数仅与OS相关,而p53蛋白积聚仅与PFS相关。Cox比例风险模型确定Akt/PKB过表达是较短PFS的显著预后因素(p = 0.0117)。

结论

这些结果表明,Akt/PKB过表达提示弥漫性星形细胞瘤的恶性进展和浸润性复发,可作为该肿瘤的新型预后标志物。

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