Expression and prognostic significance of microRNAs in Korean patients with myelodysplastic syndrome

被引:15
|
作者
Choi, Yunsuk [1 ]
Hur, Eun-Hye [2 ]
Moon, Ju Hyun [2 ]
Goo, Bon-Kwan [2 ]
Choi, Dae Ro [3 ]
Lee, Je-Hwan [2 ]
机构
[1] Univ Ulsan, Ulsan Univ Hosp, Coll Med, Dept Hematol & Oncol, Ulsan, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Hematol, 88 Olymp Ro 43 Gil, Seoul 05505, South Korea
[3] Hallym Univ, Chuncheon Sacred Heart Hosp, Dept Internal Med, Chunchon, South Korea
来源
KOREAN JOURNAL OF INTERNAL MEDICINE | 2019年 / 34卷 / 02期
关键词
Myelodysplastic syndromes; MIRN126; microRNA; human; hsa-146b-5p; MIRN155; MIRN200; HEMATOPOIETIC STEM-CELLS; SCORING SYSTEM; CANCER;
D O I
10.3904/kjim.2016.239
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Various alterations of microRNA (miRNA) expression have been reported in myelodysplastic syndrome (MDS). We aimed to investigate the unique patterns and prognostic significance of miRNA expression in Korean patients with MDS. Methods: Bone marrow mononuclear cells were collected from eight healthy controls and 26 patients with MDS, and miRNAs were isolated and assessed via quantitative real-time polymerase chain reaction for selected miRNAs, including miR-21, miR-124a, miR-126, miR-146b-5p, miR-155, miR-182, miR-200c, miR 342-5p, miR 708, and Let 7a. Results: MiR-124a, miR-155, miR-182, rniR-200c, miR-342-5p, and Let-7a were significantly underexpressed in patients with MDS, compared to healthy controls. MiR-21, miR-126, 146b-5p, and miR-155 transcript levels were significantly lower in international prognostic scoring system lower (low and intermediate-1) risk MDS than in higher (intermediate-2 and high) risk MDS. Higher expression levels of miR-126 and miR-155 correlated with significantly shorter overall survival and leukemia-free survival. Higher miR-124a expression also tended to be related to shorter survivals. Conclusions: Although our study was limited by the relatively small number of patients included, we identified several miRNAs associated with pathogenesis, leukemic transformation, and prognosis in MDS.
引用
收藏
页码:390 / 400
页数:11
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