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Expression of angiopoietin-TIE system components in angiosarcoma

机译:血管生成素-TIE系统成分在血管肉瘤中的表达

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Angiosarcoma is an aggressive malignancy of endothelial differentiation. Potential roles of the endothelial angiopoietin-tunica interna endothelial cell kinase (ANGPT-TIE) system in angiosarcoma diagnosis, pathogenesis, prognosis and treatment are undefined. To examine the expression and prognostic significance of angiopoietin-1, angiopoietin-2, TIE1 and TEK (TIE2) proteins in angiosarcoma, we immunohistochemically evaluated clinically annotated human angiosarcoma samples. Correlations of protein expression with overall survival and pathological features were explored. The cohort included 51 patients diagnosed with angiosarcoma at the age of 30–86 years (median 67). The 5-year overall survival was 45% with a median of 26 months. Moderate to strong expression of angiopoietin-1, TIE1 and TEK (TIE2) was identified in the majority of angiosarcomas and moderate to strong expression of angiopoietin-2 was observed in 42% of angiosarcomas. Increased angiopoietin-1 expression correlated with improved survival. Non-significant trends toward longer survival were also observed with increased TIE1 and TEK (TIE2) expression. Increased expression of angiopoietin-2, TIE1 and TEK (TIE2) was associated with vasoformative architecture. No differences in expression of these proteins were observed when patients were segregated by age, gender, presence or absence of metastases at diagnosis, primary tumor location, radiation association or the presence of necrosis. We conclude that components of the ANGPT-TIE system are commonly expressed in angiosarcomas. Reduced expression of these proteins is associated with non-vasoformative and clinically more aggressive lesions.
机译:血管肉瘤是内皮分化的侵袭性恶性肿瘤。内皮血管生成素-膜间质内皮细胞激酶(ANGPT-TIE)系统在血管肉瘤的诊断,发病机制,预后和治疗中的潜在作用尚不清楚。为了检查血管生成素-1,血管生成素-2,TIE1和TEK(TIE2)蛋白在血管肉瘤中的表达及其预后意义,我们通过免疫组化方法对临床注释的人血管肉瘤样本进行了评估。探索了蛋白质表达与总生存和病理特征的关系。该队列包括51名30-86岁(平均67岁)的诊断为血管肉瘤的患者。 5年总生存率为45%,中位数为26个月。在大多数血管肉瘤中发现了中度至强表达的血管生成素-1,TIE1和TEK(TIE2),在42%的血管肉瘤中观察到了中度至强表达的血管生成素-2。血管生成素-1表达增加与存活率提高相关。随着TIE1和TEK(TIE2)表达的增加,也观察到了更长寿的非显着趋势。血管生成素2,TIE1和TEK(TIE2)的表达增加与血管形成结构有关。当按年龄,性别,诊断时是否存在转移,按原发肿瘤位置,放射关联或坏死来区分患者时,未观察到这些蛋白质的表达差异。我们得出结论,ANGPT-TIE系统的成分通常在血管肉瘤中表达。这些蛋白质表达的减少与非血管形成性和临床上更具侵袭性的病变有关。

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