首页> 外文期刊>APMIS: Acta Pathologica, Microbiologica et Immunologica Scandinavica >Clinical and pathological correlations of marrow PUMA and P53 expressions in myelodysplastic syndromes
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Clinical and pathological correlations of marrow PUMA and P53 expressions in myelodysplastic syndromes

机译:骨髓增生异常综合征中骨髓PUMA和P53表达的临床和病理相关性

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摘要

p53 is a key regulator of apoptosis. p53 upregulated modulator of apoptosis (PUMA) is a critical mediator of p53-dependent and independent apoptosis. The objective of this study was to evaluate the relationship of p53 and PUMA to the prognosis of MDS. Bone marrow biopsies of MDS patients at the time of diagnosis (n=76) and at the time of transformation (n=19) were included in the study group. The expression of p53 and PUMA was evaluated using immunohistochemistry. When compared to the control group, both p53 (p<0.001) and PUMA (p=0.012) expression levels were significantly higher in MDS group. In MDS group, there was a moderate positive correlation between p53 and PUMA expressions. PUMA expression was not correlated with event free and overall survival. However, overall survival was significantly lower in cases with p53 expression in more than 50% of the cells. There was an increase in PUMA expression in cases that showed transformation as compared to the initial diagnostic bone marrows but was not statistically significant. The correlation that existed between p53 and PUMA was lost in transformed cases. Our results showed that PUMA and p53 expressions are increased in MDS marrows compared to normal marrows. PUMA expression increases further during transformation while the expression of p53 is not significantly altered which suggests that PUMA alterations might be a late event during the evolution of MDS.
机译:p53是细胞凋亡的关键调节因子。 p53上调的凋亡调节剂(PUMA)是p53依赖和独立凋亡的关键介体。这项研究的目的是评估p53和PUMA与MDS预后的关系。研究组包括诊断时(n = 76)和转化时(n = 19)的MDS患者的骨髓活检。使用免疫组织化学评估p53和PUMA的表达。与对照组相比,MDS组的p53(p <0.001)和PUMA(p = 0.012)表达水平均显着较高。在MDS组中,p53和PUMA表达之间存在中等正相关。 PUMA的表达与无事件和总生存无关。但是,在超过50%的细胞中p53表达的情况下,总生存率明显降低。与最初的诊断性骨髓相比,在显示转化的病例中,PUMA表达有所增加,但无统计学意义。在转化病例中,p53和PUMA之间存在的相关性丢失了。我们的结果表明,与正常骨髓相比,MDS骨髓中PUMA和p53表达增加。 PUMA表达在转化过程中进一步增加,而p53的表达没有明显改变,这表明PUMA改变可能是MDS进化过程中的晚期事件。

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