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首页> 外文期刊>Virchows Archiv: an international journal of pathology >Epithelial cell adhesion molecules and epithelial mesenchymal transition (EMT) markers in Ewing's sarcoma family of tumors (ESFTs). Do they offer any prognostic significance?
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Epithelial cell adhesion molecules and epithelial mesenchymal transition (EMT) markers in Ewing's sarcoma family of tumors (ESFTs). Do they offer any prognostic significance?

机译:尤因氏肉瘤家族的肿瘤(ESFT)中的上皮细胞粘附分子和上皮间质转化(EMT)标记。它们是否具有预后意义?

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摘要

Epithelial marker and adhesion molecule expression has been reported in Ewing's sarcoma family of tumors (ESFTs), although the prognostic significance has not been assessed systematically.We performed immunohistochemical analysis of epithelial cell adhesion molecule and epithelial mesenchymal transition markers on 415 genetically confirmed ESFTs. Survival analyses were performed in 217 patients. The atypical histological subtype expressed a high proportion of the epithelial markers compared with conventional and PNET variants. We observed that expression of desmoplakin (p<0.001) and PI3K (p=0.003) was higher in disseminated than in localized disease. Multivariate analysis showed that desmoplakin and pGSK3β constitute independent good prognostic factors for progression free survival (PFS), while ZO-1 and Snail represent independent good prognostic factors for overall survival (OS). In contrast, CK8/18 represents an independent poor prognostic factor for OS and the radiotherapy treatment group demonstrated an independent poor prognostic factor for PFS and OS. Although the expression of pan-cytokeratin has been previously highlighted in a significant proportion of ESFT, its expression did not reveal prognostic significance in the present series. Considering the results of prognostic analysis herein reported, we strongly recommend a prospective validation of at least the immunomarkers with prognostic significance (desmoplakin, ZO-1, CK8/18, pGSK3β, and Snail) in prospective series that include localized and disseminated tumors.
机译:尽管尚未系统评估预后的意义,但在尤因氏肉瘤家族(ESFTs)中已有上皮标记物和粘附分子表达的报道。我们对415例经遗传学证实的ESFTs进行了上皮细胞粘附分子和上皮间质转化标记物的免疫组织化学分析。对217例患者进行了生存分析。与常规和PNET变体相比,非典型组织学亚型表达了较高比例的上皮标志物。我们观察到,在传播性疾病中,desmoplakin(p <0.001)和PI3K(p = 0.003)的表达高于局部疾病。多变量分析表明,desmoplakin和pGSK3β构成了无进展生存期(PFS)的独立良好预后因素,而ZO-1和Snail代表了总体生存期(OS)的独立良好预后因素。相反,CK8 / 18代表OS的独立不良预后因素,放疗治疗组证明PFS和OS的独立不良预后因素。尽管泛细胞角蛋白的表达先前已在相当大的ESFT中得到了强调,但其表达在本系列文章中并未显示出预后意义。考虑到本文报道的预后分析结果,我们强烈建议至少对具有局部和弥散性肿瘤的前瞻性系列免疫标志物(desmoplakin,ZO-1,CK8 / 18,pGSK3β和Snail)进行前瞻性验证。

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