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使用分子标记和免疫组织化学进行肝细胞腺瘤亚型分类

Hepatocellular adenoma subtype classification using molecular markers and immunohistochemistry.

作者信息

Bioulac-Sage Paulette, Rebouissou Sandra, Thomas Cristel, Blanc Jean-Frédéric, Saric Jean, Sa Cunha Antonio, Rullier Anne, Cubel Gaëlle, Couchy Gabrielle, Imbeaud Sandrine, Balabaud Charles, Zucman-Rossi Jessica

机构信息

Department of Pathology, CHU Bordeaux, France.

出版信息

Hepatology. 2007 Sep;46(3):740-8. doi: 10.1002/hep.21743.

Abstract

UNLABELLED

Hepatocellular adenomas (HCA) with activated beta-catenin present a high risk of malignant transformation. To permit robust routine diagnosis to allow for HCA subtype classification, we searched new useful markers. We analyzed the expression of candidate genes by quantitative reverse transcription polymerase chain reaction QRT-PCR followed by immunohistochemistry to validate their specificity and sensitivity according to hepatocyte nuclear factor 1 alpha (HNF1alpha) and beta-catenin mutations as well as inflammatory phenotype. Quantitative RT-PCR showed that FABP1 (liver fatty acid binding protein) and UGT2B7 were downregulated in HNF1alpha-inactivated HCA (P <or= 0.0002); GLUL (glutamine synthetase) and GPR49 overexpression were associated with beta-catenin-activating mutations (P <or= 0.0005), and SAA2 (serum amyloid A2) and CRP (C-reactive protein) were upregulated in inflammatory HCA (P = 0.0001). Immunohistochemistry validation confirmed that the absence of liver-fatty acid binding protein (L-FABP) expression rightly indicated HNF1alpha mutation (100% sensitivity and specificity), the combination of glutamine synthetase overexpression and nuclear beta-catenin staining were excellent predictors of beta-catenin-activating mutation (85% sensitivity, 100% specificity), and SAA hepatocytic staining was ideal to classify inflammatory HCA (91% sensitivity and specificity). Finally, a series of 93 HCA was unambiguously classified using our 4 validated immunohistochemical markers. Importantly, new associations were revealed for inflammatory HCA defined by SAA staining with frequent hemorrhages (P = 0.003), telangiectatic phenotype (P < 0.001), high body mass index, and alcohol intake (P <or= 0.04). Previously described associations were confirmed and in particular the significant association between beta-catenin-activated HCA and hepatocellular carcinomas (HCC) at diagnosis or during follow-up (P < 10(-5)).

CONCLUSION

We refined HCA classification and its phenotypic correlations, providing a routine test to classify hepatocellular adenomas using simple and robust immunohistochemistry.

摘要

未标记

具有激活的β-连环蛋白的肝细胞腺瘤(HCA)具有较高的恶性转化风险。为了进行可靠的常规诊断以实现HCA亚型分类,我们寻找了新的有用标志物。我们通过定量逆转录聚合酶链反应(QRT-PCR)分析候选基因的表达,随后进行免疫组织化学,以根据肝细胞核因子1α(HNF1α)和β-连环蛋白突变以及炎症表型验证其特异性和敏感性。定量RT-PCR显示,FABP1(肝脂肪酸结合蛋白)和UGT2B7在HNF1α失活的HCA中下调(P≤0.0002);GLUL(谷氨酰胺合成酶)和GPR49的过表达与β-连环蛋白激活突变相关(P≤0.0005),SAA2(血清淀粉样蛋白A2)和CRP(C反应蛋白)在炎症性HCA中上调(P = 0.0001)。免疫组织化学验证证实,肝脂肪酸结合蛋白(L-FABP)表达缺失正确表明HNF1α突变(敏感性和特异性均为100%),谷氨酰胺合成酶过表达与细胞核β-连环蛋白染色相结合是β-连环蛋白激活突变的优秀预测指标(敏感性85%,特异性100%),SAA肝细胞染色是对炎症性HCA进行分类的理想方法(敏感性和特异性均为91%)。最后,使用我们的4种经过验证的免疫组织化学标志物对一系列93例HCA进行了明确分类。重要的是,发现SAA染色定义的炎症性HCA与频繁出血(P = 0.003)、毛细血管扩张表型(P < 0.001)、高体重指数和饮酒(P≤0.04)之间存在新的关联。先前描述的关联得到了证实,特别是β-连环蛋白激活的HCA与诊断时或随访期间的肝细胞癌(HCC)之间的显著关联(P < 10^-5)。

结论

我们完善了HCA分类及其表型相关性,提供了一种使用简单且可靠的免疫组织化学对肝细胞腺瘤进行分类的常规检测方法。

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