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小儿骨髓增生异常综合征伴急性骨髓纤维化中炎症和巨核细胞因子的分子谱。

Molecular profile of inflammatory and megakaryocytic factors in pediatric myelodysplastic syndrome with acute myelofibrosis.

机构信息

Institute of Pathology, Hannover Medical School, Hannover, Germany.

Division of Pediatric Hematology and Oncology, University Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany.

出版信息

Pediatr Blood Cancer. 2018 Jul;65(7):e27048. doi: 10.1002/pbc.27048. Epub 2018 Apr 18.

Abstract

Pediatric fibrotic myelodysplastic syndromes (ped-MDS-MF) and pediatric primary myelofibrosis (ped-PMF) are rare, and the molecular changes which mediate fibrosis have never been investigated. Histology and gene expression profile of 119 fibrosis/angiogenesis/inflammation/megakaryopoiesis-related factors in bone marrow biopsies were performed (two ped-MDS-MF and one ped-PMF). In one progressive ped-MDS, comparison of MF grade 0 (no myelofibrosis) and MF grade 2 (dense network of reticulin fibres) after 4 months showed that expression of fibrosis-related transcripts increased and dysplastic megakaryocytes formed a dense net of CD42b proplatelets. These changes were not observed in another ped-MDS-MF, whereas ped-PMF showed a similar proplatelet pattern. These findings indicate that fibrotic changes in ped-MDS may involve proplatelet-related and unrelated pathways.

摘要

儿科纤维性骨髓增生异常综合征(ped-MDS-MF)和儿科原发性骨髓纤维化(ped-PMF)较为罕见,介导纤维化的分子变化从未被研究过。对 119 例骨髓活检中与纤维化、血管生成、炎症和巨核细胞生成相关的因素进行了组织学和基因表达谱分析(2 例 ped-MDS-MF 和 1 例 ped-PMF)。在一例进行性 ped-MDS 中,比较了 MF 0 级(无骨髓纤维化)和 MF 2 级(网状纤维密集)4 个月后的结果,发现纤维化相关转录物的表达增加,并且发育异常的巨核细胞形成了密集的 CD42b 血小板网络。这些变化在另一个 ped-MDS-MF 中没有观察到,而 ped-PMF 则显示出类似的血小板网络形成模式。这些发现表明 ped-MDS 中的纤维化变化可能涉及与血小板相关和不相关的途径。

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