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CD34、RAB20、PU.1和GFI1 mRNA在骨髓增生异常综合征中的表达

CD34, RAB20, PU.1 and GFI1 mRNA expression in myelodysplastic syndrome.

作者信息

Huh H J, Chae S L, Lee M, Hong K S, Mun Y C, Seong C M, Chung W S, Huh J W

机构信息

Department of Laboratory Medicine, Dongguk University, College of Medicine, Goyang, Korea.

出版信息

Int J Lab Hematol. 2009 Jun;31(3):344-51. doi: 10.1111/j.1751-553X.2008.01056.x. Epub 2008 Mar 25.

Abstract

Myelodysplastic syndrome (MDS) with hypocellular bone marrow (BM) is often difficult to distinguish from aplastic anemia (AA). Furthermore, the diagnosis of MDS with low blast counts and normal karyotype may be problematic. These issues highlight the need for a reliable marker for the diagnosis of MDS. This study was conducted to determine if changes of mRNA expression in any of the four selected genes would be useful markers for differentiation of hypoplastic MDS from AA, and MDS from benign disease, as well as to investigate whether mRNA expressions differ between MDS risk subgroups. Thirty-five patients diagnosed with MDS, 27 patients with AA and 17 patients with benign diseases were included. The CD34, RAB20, PU.1 and GFI1 mRNA levels were measured by real-time RT-PCR. The CD34 mRNA expressions in hypoplastic MDS were higher than those found in AA. PU.1 and GFI1 mRNA expressions were significantly lower in MDS with low blast counts and normal karyotype than those of benign disease. High-risk MDS showed higher CD34 expressions than those of low-risk MDS. This study suggests that measurement of CD34 and GFI1 mRNA expressions could be useful as a diagnostic and prognostic marker for MDS.

摘要

骨髓细胞减少的骨髓增生异常综合征(MDS)常难以与再生障碍性贫血(AA)相鉴别。此外,原始细胞计数低且核型正常的MDS的诊断可能存在问题。这些问题凸显了需要一种可靠的标志物来诊断MDS。本研究旨在确定所选四个基因中任何一个基因的mRNA表达变化是否可作为区分低增生性MDS与AA、MDS与良性疾病的有用标志物,并研究MDS风险亚组之间的mRNA表达是否存在差异。研究纳入了35例诊断为MDS的患者、27例AA患者和17例良性疾病患者。通过实时逆转录聚合酶链反应(RT-PCR)检测CD34、RAB20、PU.1和GFI1的mRNA水平。低增生性MDS中的CD34 mRNA表达高于AA中的表达。原始细胞计数低且核型正常的MDS中PU.1和GFI1 mRNA表达显著低于良性疾病中的表达。高危MDS的CD34表达高于低危MDS。本研究表明,检测CD34和GFI1 mRNA表达可作为MDS的诊断和预后标志物。

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