›› 2014, Vol. 32 ›› Issue (12): 1145-.doi: 10.3969 j.issn.1000-3606.2014.12.012

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The expressions of miR-196b and its prognostic significances in pediatric acute myeloid leukemia

XU Lihua 1,3,CEN Jiannong2, HE Hailong1, SHEN Hongjie2, YANG Naichao1, YAN Qing1, HU Shaoyan1   

  1. 1. Department of Hematology and Oncology, Affiliated Children’ s Hospital of Soochow University, Suzhou 215003, Jiangsu, China; 2. Department of Hematology,Jiangsu Institute of Hematology, The First Hospital Affiliated to Soochow University, Suzhou 215006, Jiangsu, China; 3.Department of Pediatrics, The First People’s Hospital of Lianyungang, Lianyungang 222002, Jiangsu, China
  • Received:2014-12-15 Online:2014-12-15 Published:2014-12-15

Abstract: Objective To evaluate the expression of miR-196b in newly diagnosed pediatric acute myeloid leukemia (AML) and its clinical significance. Methods Fifty-two AML children were enrolled in this study and 30 non-leukemia compared children were selected as controls. The expressions of miR-196b were detected in bone marrow samples by real-time quantitative PCR (q-RT-PCR) and the results were expressed in 2-ΔΔCt. Results miR-196b expressions were significantly higher in M4-5 and lower in non- M4-5 of AML children than those in control (P<0.01), with a lowest level in t (15;17) and a highest level in MLL subtypes (P<0.01). The miR-196b expressions were significantly different among different prognosis groups (P<0.01) and the level in the favorable prognostic group was lower than in poor prognosis group. It was also found that miR-196b expression was lower in remission group than that in no-remission group after the first induction remission therapy (P<0.05). Meanwhile, the expression of miR-196b in the children with WBC≥100×109/L were statistically higher than that in the children with WBC<100×109/L (P<0.01), and miR-196b level was positively correlated with the platelet counts (r=0.302, P=0.030). Conclusions miR-196b expression is increased in poor prognosis group of AML children, and high expression of miR-196b is related with low response rate and poor prognosis. miR-1966 is expected to become a new target for the treatment of AML.