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Stat3-positive tumor cells contribute to vessels neoformation in primary central nervous system lymphoma

机译:Stat3阳性肿瘤细胞促进原发性中枢神经系统淋巴瘤的血管新生

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摘要

With the aim of elucidating the relationship between Stat3 expression and tumor vessels abnormalities in the PCNLs, in this study we evaluated Stat3 and pStat3 expression by Real-time PCR and by immunohistochemistry in biopsy sections from PCNSL patients. Correlations of the expression levels with the presence of aberrant vessels were analyzed by confocal laser microscopy analysis, using FVIII as endothelial cell marker, CD133 and nestin as cancer stem cell (CSC) marker, CD20 as tumor cell marker, and Stat3. In addition, we investigated Stat3 mutations in lymphoma cells to clarify the role of the constitutive expression of Stat3 and of its phosphorylated forms. Results showed that in PCNSL, putative endothelial cells lining the vessels are heterogeneous, expressing FVIII/ pStat3/CD133 (presumably originally they are vascular progenitor cells), as well as FVIII/CD20/CD133 (presumably originally they are tumor cells). Finally, we detected a fraction of the FVIII+ endothelial cell that co-expressed Stat3 bearing a tetraploid karyotype, while no amplification signal for the Stat3 gene was detected.
机译:为了阐明Stat3表达与PCNLs中肿瘤血管异常之间的关系,在本研究中,我们通过实时PCR和免疫组织化学方法对PCNSL患者的活检切片评估了Stat3和pStat3表达。通过共聚焦激光显微镜分析法分析表达水平与异常血管存在的相关性,使用FVIII作为内皮细胞标记,CD133和nestin作为癌症干细胞(CSC)标记,CD20作为肿瘤细胞标记和Stat3。此外,我们调查了淋巴瘤细胞中的Stat3突变,以阐明Stat3的组成型表达及其磷酸化形式的作用。结果表明,在PCNSL中,位于血管内的假定的内皮细胞是异质的,表达FVIII / pStat3 / CD133(可能最初是血管祖细胞)以及FVIII / CD20 / CD133(可能最初是肿瘤细胞)。最后,我们检测到一部分FVIII + 内皮细胞共表达带有四倍体核型的Stat3,而没有检测到Stat3基因的扩增信号。

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