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首页> 外文期刊>Journal of Breast Cancer >Notch1 in Tumor Microvascular Endothelial Cells and Tumoral miR-34a as Prognostic Markers in Locally Advanced Triple-Negative Breast Cancer
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Notch1 in Tumor Microvascular Endothelial Cells and Tumoral miR-34a as Prognostic Markers in Locally Advanced Triple-Negative Breast Cancer

机译:Notch1在肿瘤微血管内皮细胞和肿瘤miR-34a中作为局部晚期三阴性乳腺癌的预后标志物

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Purpose Triple-negative breast cancer (TNBC) is associated with poor prognosis with limited treatment options. Angiogenesis is known to be involved in the progression of TNBC, and targeting this pathway results in modest clinical benefits. In this study, we analyzed the role of tumor microvascular endothelial Notch1 (EC Notch1) and tumoral miR-34a as prognostic markers in patients with TNBC. Methods The expression of miR-34a was analyzed using archival tumor tissues from 114 patients with TNBC. Simultaneously, archival tumor tissues were also checked for the expression of CD34 and Notch1 by immunostaining. The ratio of Notch1-microvascular density (MVD) to CD34-MVD was defined as EC Notch1. The association between the expression of miR-34a or EC Notch1 and clinicopathological characteristics was analyzed. Results In the overall patient population, patients with low expression of EC Notch1 was associated with better overall survival (OS, p = 0.041) than those with high expression of EC Notch1. In lymph node-positive TNBC patients, high levels of miR-34a and low levels of EC Notch1 correlated significantly with higher survival benefits in terms of OS ( p = 0.026), disease-free survival ( p = 0.009), and metastasis-free survival ( p = 0.038) relative to that in other patients. Decreased expression of EC Notch1 and increased expression of miR-34a also showed a survival benefit in locally advanced TNBC. Conclusion The fact that miR-34a and EC Notch1 are associated with the angiogenesis suggests that angiogenesis may play a role in the development and progression of TNBC.
机译:目的三阴性乳腺癌(TNBC)与不良预后以及有限的治疗选择相关。已知血管生成与TNBC的发展有关,靶向该途径可产生适度的临床益处。在这项研究中,我们分析了肿瘤微血管内皮Notch1(EC Notch1)和肿瘤miR-34a作为TNBC患者的预后标志物的作用。方法用114例TNBC患者的档案肿瘤组织分析miR-34a的表达。同时,还通过免疫染色检查了档案肿瘤组织中CD34和Notch1的表达。将Notch1-微血管密度(MVD)与CD34-MVD之比定义为EC Notch1。分析了miR-34a或EC Notch1的表达与临床病理特征之间的关系。结果在总的患者人群中,低表达EC Notch1的患者比高表达EC Notch1的患者具有更好的总体生存率(OS,p = 0.041)。在淋巴结阳性TNBC患者中,高水平的miR-34a和低水平的EC Notch1与OS(p = 0.026),无病生存(p = 0.009)和无转移的生存获益显着相关。相对于其他患者的生存率(p = 0.038)。 EC Notch1的表达减少和miR-34a的表达增加在局部晚期TNBC中也显示出生存优势。结论miR-34a和EC Notch1与血管生成有关的事实表明,血管生成可能在TNBC的发展和进程中起作用。

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