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Epithelial cell adhesion molecule and epithelial-mesenchymal transition are associated with vasculogenic mimicry poor prognosis and metastasis of triple negative breast cancer

机译:上皮细胞粘附分子和上皮间质转化与血管生成拟态预后不良和三阴性乳腺癌的转移有关

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摘要

Triple-negative breast cancer (TNBC) is associated with epithelial-mesenchymal transition (EMT) and the phenotype of breast cancer stem cells (CSCs). Vasculogenic mimicry (VM) is a novel pattern of tumor blood supply and associated with aggression and metastasis of TNBC. Previous studies have shown that both CSCs and EMT are associated with VM, although the underlying mechanism is yet unclear. The present study aimed to analyze the immunohistochemical (IHC) expression of CSC marker, epithelial cell adhesion molecule (EpCAM), EMT-related markers, including transcription factors (TFs) (Slug, Twist1, and ZEB1), and EMT markers (E-cadherin and vimentin) in 137 TNBC. The expression of these markers was correlated to the clinicopathological features and VM channels of the tumors, including patient overall survival (OS) and disease-free survival (DFS). Furthermore, the expression of EpCAM and EMT-related markers showed a positive correlation with distant metastasis and lymph node metastasis ( < 0.05). A significant association was noted between VM and histological grade ( = 0.007). Moreover, VM showed a significant positive correlation with EpCAM, EMT-associated TFs, and VE-cadherin expression in TNBC. Furthermore, binary logistic analysis showed that VM expression was significantly correlated with lymph node metastasis and distant metastasis ( < 0.05). In survival analysis, the overexpression of EpCAM and ZEB1 predicted a poor prognosis with respect to OS and DFS. In addition, the presence of VM was significantly associated with poor OS and DFS. Multivariate Cox regression analysis revealed that VM expression is an independent prognostic factor for TNBC patients. In summary, VM was confirmed as a potential biomarker for TNBC associated with poor clinical outcomes and tumor metastasis. This study also suggested that EpCAM protein might be involved in VM formation by EMT in TNBC.
机译:三阴性乳腺癌(TNBC)与上皮间质转化(EMT)和乳腺癌干细胞(CSCs)的表型有关。血管生成模拟(VM)是肿瘤血液供应的一种新型模式,与TNBC的侵袭和转移有关。先前的研究表明,CSC和EMT均与VM相关联,尽管其潜在机制尚不清楚。本研究旨在分析CSC标记,上皮细胞粘附分子(EpCAM),EMT相关标记(包括转录因子(TFs)(Slug,Twist1和ZEB1))和EMT标记(E-钙粘蛋白和波形蛋白)在137 TNBC中。这些标志物的表达与肿瘤的临床病理特征和VM通道相关,包括患者的总生存期(OS)和无病生存期(DFS)。此外,EpCAM和EMT相关标志物的表达与远处转移和淋巴结转移呈正相关(<0.05)。 VM与组织学分级之间存在显着相关性(= 0.007)。此外,VM与TNBC中的EpCAM,EMT相关的TF和VE-钙黏着蛋白表达呈显着正相关。此外,二元逻辑分析表明,VM表达与淋巴结转移和远处转移显着相关(<0.05)。在生存分析中,EpCAM和ZEB1的过表达预示着OS和DFS的预后不良。此外,VM的存在与不良的OS和DFS显着相关。多变量Cox回归分析显示,VM表达是TNBC患者的独立预后因素。总之,VM被确认为与不良临床结果和肿瘤转移相关的TNBC的潜在生物标志物。这项研究还表明,EpCAM蛋白可能与TNBC中EMT参与的VM形成有关。

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