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早期胃癌患者免疫组化标志物表达与组织学类型的关系

Expression of immunohistochemical markers according to histological type in patients with early gastric cancer.

作者信息

Han Jae Pil, Hong Su Jin, Kim Hee Kyung, Kim Hyun Su, Lee Yun Nah, Lee Tae Hee, Lee Joon Seong

机构信息

a 1 Digestive Disease Center and Research Institute, Department of Internal Medicine, Soonchunhyang University College of Medicine , Bucheon, Korea.

b 2 Department of Pathology, Soonchunhyang University College of Medicine , Bucheon, Korea.

出版信息

Scand J Gastroenterol. 2016 Jan;51(1):60-6. doi: 10.3109/00365521.2015.1065510. Epub 2015 Jul 4.

Abstract

OBJECTIVE

We compared the biological characteristics of early gastric cancer (EGC) using immunohistochemical (IHC) staining among histological types.

MATERIALS AND METHODS

IHC staining results were analyzed in 86 EGCs resected with endoscopic submucosal dissection to identify mucin phenotype and biological characteristics.

RESULTS

The histological type was classified as tubular adenocarcinoma (TAC), mixed adenocarcinoma (MAC), or poorly cohesive carcinoma (PCC). Significant differences in MUC-2 (34.4% vs. 10.7%, p < 0.05) and MUC-5AC (59.4% vs. 85.7%, p < 0.05) expression were observed between TAC and PCC. The poorly cohesive component of MAC showed stronger immunoreactivity to CD10 (46.2% vs. 14.3%, p < 0.05) but weaker reactivity to MUC-5AC (57.7% vs. 85.7%, p < 0.05), compared to that of PCC. E-cadherin and β-catenin expression levels significantly decreased in the poorly cohesive component of MAC (15.4% vs. 90.6%, p < 0.05; 7.7% vs. 90.6%, p < 0.05, respectively) and PCC (10.7% vs. 90.6%, p < 0.05; 14.3% vs. 90.6%, p < 0.05, respectively), compared to TAC. However, vascular endothelial growth factor expression significantly increased in the poorly cohesive component of MAC (42.3% vs. 9.4%, p < 0.05) and PCC (39.3% vs. 9.4%, p < 0.05), compared to TAC.

CONCLUSION

IHC analysis showed that EGC histological types differ in terms of mucin phenotype and biological characteristics. The poorly cohesive components showed decreased E-cadherin and β-catenin expression levels and increased vascular endothelial growth factor expression. These characteristics may contribute to the poor prognosis of patients with MAC and PCC.

摘要

目的

我们通过免疫组织化学(IHC)染色比较了早期胃癌(EGC)不同组织学类型的生物学特性。

材料与方法

对86例接受内镜下黏膜下剥离术切除的EGC进行IHC染色结果分析,以确定黏蛋白表型和生物学特性。

结果

组织学类型分为管状腺癌(TAC)、混合腺癌(MAC)或低黏附性癌(PCC)。TAC和PCC之间在MUC-2(34.4%对10.7%,p<0.05)和MUC-5AC(59.4%对85.7%,p<0.05)表达上存在显著差异。与PCC相比,MAC的低黏附成分对CD10的免疫反应性更强(46.2%对14.3%,p<0.05),但对MUC-5AC的反应性较弱(57.7%对85.7%,p<0.05)。与TAC相比,MAC(分别为15.4%对90.6%,p<0.05;7.7%对90.6%)和PCC(分别为10.7%对90.6%,p<0.05;14.3%对90.6%)的低黏附成分中E-钙黏蛋白和β-连环蛋白表达水平显著降低。然而,与TAC相比,MAC(42.3%对9.4%)和PCC(39.3%对9.4%)的低黏附成分中血管内皮生长因子表达显著增加(p<0.05)。

结论

IHC分析表明,EGC组织学类型在黏蛋白表型和生物学特性方面存在差异。低黏附成分显示E-钙黏蛋白和β-连环蛋白表达水平降低,血管内皮生长因子表达增加。这些特性可能导致MAC和PCC患者预后不良。

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