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首页> 外文期刊>Pediatric Hematology and Oncology >Characterization of bone marrow stromal abnormalities in a patient with constitutional trisomy 8 mosaicism and myelodysplastic syndrome.
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Characterization of bone marrow stromal abnormalities in a patient with constitutional trisomy 8 mosaicism and myelodysplastic syndrome.

机译:体质三体性8号镶嵌症和骨髓增生异常综合症患者的骨髓基质异常特征。

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摘要

The development of myeloid leukemias and myelodysplastic syndrome (MDS) is common in children with trisomy 8 mosaicism. However, the mechanisms by which the presence of an additional chromosome 8 translates to an increased risk of leukemias and MDS is currently unknown. The authors describe the analysis of stromal cells from a pediatric MDS patient with constitutional trisomy 8. Patient and control marrow stromal cells were analyzed for alterations in cytokine production. Clonogenic assays were used to examine stromal support for hematopoiesis. The interplay between leukemia cells and stroma was studied by co-culture experiments. The results indicate that stromal cell function in this patient was seriously altered in favor of progenitor cell proliferation and expansion. This indicates that constitutional trisomy 8 in stromal cells plays a critical role in the pathogenesis of MDS.
机译:骨髓性白血病和骨髓增生异常综合症(MDS)的发生在三体性8号镶嵌症患儿中很常见。然而,目前尚不知道存在额外的染色体8会导致白血病和MDS风险增加的机制。作者描述了患有三体三体综合征的小儿MDS患者的基质细胞的分析,分析了患者和对照骨髓基质细胞的细胞因子产生变化。克隆试验用于检查造血功能的基质支持。通过共培养实验研究了白血病细胞与基质之间的相互作用。结果表明该患者的基质细胞功能发生了严重变化,有利于祖细胞的增殖和扩增。这表明基质细胞中的8三体性在MDS的发病机理中起着至关重要的作用。

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