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颅咽管瘤中碳酸酐酶 IX 的表达。

Expression of carbonic anhydrase IX in craniopharyngiomas.

机构信息

Department of Neurosurgery, University Regensburg Medical Center, Regensburg, Germany.

出版信息

J Neurosurg. 2011 Oct;115(4):796-801. doi: 10.3171/2011.6.JNS1168. Epub 2011 Jul 15.

DOI:10.3171/2011.6.JNS1168
PMID:21761968
Abstract

OBJECT

In craniopharyngiomas, cystic growth causes pressure on vital structures of the adjacent brain, leading to significant morbidity. However, the molecular pathogenesis of this cyst formation remains unknown. Carbonic anhydrase IX (CA IX) is a tumor-associated, hypoxia-inducible enzyme, which can cause fluid production and development of cysts. The authors investigated CA IX expression in craniopharyngiomas and its correlation with the extent of cyst formation. In addition, the major pathways of CA IX regulation, hypoxia and p53 mutation, were analyzed.

METHODS

Expression of CA IX was analyzed in 20 craniopharyngioma patients by means of in situ hybridization and immunohistochemistry. Preoperative imaging was used to quantify cyst volume. To analyze putative hypoxic induction of CA IX, immunohistochemical staining for HIF-1α and VEGF was performed. Since p53 negatively regulates CA IX expression, we also analyzed the tumors for p53 mutation by direct sequencing.

RESULTS

Significant CA IX was found in 85% of the 20 cases. The extent of CA IX expression was significantly correlated with cyst volume. HIF-1α expression was largely absent in all tissue samples, whereas moderate VEGF expression was present in a subset of cases but without correlation to cyst volume. No p53 mutation was found in any of the analyzed tumors.

CONCLUSIONS

Carbonic anhydrase IX, which is virtually absent in normal brain, is significantly upregulated in craniopharyngiomas and shows a significant association with cyst size. The mechanisms of regulation remain unknown, since neither hypoxia nor p53 appears to play a role. These results indicate that inhibition of CA IX may be a potential target for the adjuvant treatment in patients with cystic craniopharyngiomas.

摘要

目的

颅咽管瘤的囊性生长导致毗邻脑内重要结构受压,引起严重的发病率。然而,这种囊形成的分子发病机制尚不清楚。碳酸酐酶 IX(CAIX)是一种与肿瘤相关的、缺氧诱导的酶,可导致液体产生和囊肿的发展。作者研究了颅咽管瘤中 CAIX 的表达及其与囊形成程度的相关性。此外,还分析了 CAIX 调节的主要途径,即缺氧和 p53 突变。

方法

采用原位杂交和免疫组织化学方法分析 20 例颅咽管瘤患者的 CAIX 表达。利用术前影像学检查来量化囊体积。为了分析 CAIX 可能的缺氧诱导,进行了 HIF-1α 和 VEGF 的免疫组织化学染色。由于 p53 负调节 CAIX 的表达,我们还通过直接测序分析了肿瘤中的 p53 突变。

结果

在 20 例病例中,有 85%的病例发现了明显的 CAIX。CAIX 表达的程度与囊体积显著相关。所有组织样本中 HIF-1α 的表达基本缺失,而在一部分病例中存在中度 VEGF 表达,但与囊体积无相关性。在分析的所有肿瘤中均未发现 p53 突变。

结论

碳酸酐酶 IX 在正常脑中几乎不存在,但在颅咽管瘤中显著上调,并与囊肿大小呈显著相关性。调节机制尚不清楚,因为缺氧和 p53 似乎都不起作用。这些结果表明,抑制 CAIX 可能是囊性颅咽管瘤患者辅助治疗的一个潜在靶点。

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