切换至 "中华医学电子期刊资源库"

中华妇幼临床医学杂志(电子版) ›› 2012, Vol. 08 ›› Issue (03) : 308 -311. doi: 10.3877/cma.j.issn.1673-5250.2012.03.016

所属专题: 文献

论著

microRNA-16在儿童急性B淋巴细胞白血病中的表达及预后意义的研究
刘秀琴1, 孙立荣2,*,*(), 张腾龙2   
  1. 1. 266021 山东青岛,青岛大学医学院附属医院儿科;青岛市立医院儿科
    2. 266021 山东青岛,青岛大学医学院附属医院儿科
  • 收稿日期:2012-03-01 修回日期:2012-05-04 出版日期:2012-06-01
  • 通信作者: 孙立荣

Expression and Significance of MicroRNA -16 in Childhood B-Cell Acute Lymphoblastic Leukemia

Xiu-qin LIU1, Li-rong SUN2(), Teng-long ZHANG2   

  1. 1. Department of Pediatrics, Affiliated Hospital of Medical College, Qingdao University, Qingdao 266071, Shandong Province, China
  • Received:2012-03-01 Revised:2012-05-04 Published:2012-06-01
  • Corresponding author: Li-rong SUN
  • About author:
    (Corresponding author: SUN Li-rong, Email: )
引用本文:

刘秀琴, 孙立荣, 张腾龙. microRNA-16在儿童急性B淋巴细胞白血病中的表达及预后意义的研究[J]. 中华妇幼临床医学杂志(电子版), 2012, 08(03): 308-311.

Xiu-qin LIU, Li-rong SUN, Teng-long ZHANG. Expression and Significance of MicroRNA -16 in Childhood B-Cell Acute Lymphoblastic Leukemia[J]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2012, 08(03): 308-311.

目的

通过检测microRNA (miR)-16在急性B淋巴细胞白血病(B-ALL)患儿骨髓单个核细胞(BMMNCs)中的表达水平,分析miR-16在不同组B-ALL患儿中的表达差异,探讨miR-16在B-ALL的发生发展及预后中的意义。

方法

收集2006年10月至2010年10月在青岛大学医学院附属医院儿科和青岛市立医院儿科初诊为B-ALL的36例患儿及12例健康儿童的骨髓标本为研究对象,分别纳入研究组和对照组。对研究组36例B-ALL患儿进行髂后上嵴穿刺获取BMMNCs,最终确诊为B-ALL高危标本为13例,标危标本为23例,分别纳入高危组和标危组。对研究组分别于化疗前、后采集标本进行实时(real-time)荧光定量PCR法检测BMMNCs中miR-16表达。对化疗后miR-16表达明显升高的30例患儿标本,纳入化疗敏感组,其余6例,纳入化疗耐药组(本研究遵循的程序符合本院人体试验委员会所制定的伦理学标准,得到该委员会批准)。

结果

①miR-16在研究组的表达水平明显低于对照组,高危组明显低于标危组,差异均有统计学意义(P<0.05);② B-ALL患儿化疗后,miR-16表达水平较化疗前明显升高,差异有统计学意义(P<0.05),其中以化疗敏感组升高最为明显(P<0.05),化疗耐药组化疗前、后miR-16表达水平比较,差异统计学意义(P>0.05)。

结论

miR-16低表达在B-ALL发病中发挥着重要作用,与白血病细胞增殖、转移能力和预后密切相关,可作为判断B-ALL患儿预后指标之一。

Objective

To explore the expression of microRNA (miR)-16 in bone marrow mono-nuclear cells (BMMNCs) of childhood B-cell acute lymphoblastic leukemia (B-ALL).

Methods

From October 2006 to October 2010, a total of 36 cases of childhood B-ALL bone marrow prepares (study group) and normal samples from 12 healthy children (control group) were admitted in the Department of Pediatrics, Affiliated Hospital of Medical College, Qingdao University and Qingdao Municipal Hospital. According to results of posterior superior iliac crest puncture to obtain BMMNCs, high risk bone marrow prepares were included into high risk group(n=13), standard risk bone marrow prepares were included into high risk group(n=23). Expression levels of miR-16 in BMMNCs of childhood B-ALL children before and after chemical therapy were examined by real-time polymerase chain reaction(real-time PCR) and the correlations between the expression levels of miR-16 and related subgroup were further analyzed. Expression levels of miR-16 had statistically significant increase after chemical therapy were included into sensitive group(n=30), the others were included into chemotherapy resistant group(n=6).

Results

Expression levels of miR-16 in study group were higher than those in control group, especially in high risk group (P<0.05). Expression levels of miR-16 in childhood B-ALL patients increased after chemical therapy than those before treatment, especially in sensitive group (P<0.05). There was no statistically significant change in chemotherapy resistant group after chemical therapy(P>0.05).

Conclusions

MiR-16 plays an important role in the development of childhood B-ALL. Low-regulated expression of miR-16 was associated with poor prognosis.

图1 实时荧光定量PCR检测miR -16在各组BMMNC中的相对表达水平比较(A:研究组化疗前、后研究组BMMNC中miR -16表达水平。B:对照组、敏感组化疗后与耐药前化疗后BMMNC中miR -16表达水平)
Figure 1 Expression levels of miR-16 in bone marrow mono-nuclear cells of childhood B-ALL were examined by real-time polymerase chain reaction
图2 实时荧光定量PCR检测miR-16在各组BMMNC中化疗前、后表达比较(A:研究组化疗前、后研究组BMMNC中miR -16表达水平。B:对照组与敏感组化疗前、后,耐药组化疗前、后BMMNC中miR -16表达水平)
Figure 2 Correlations between the expression levels of miR-16 and related subgroup
[1]
Turner ML, Schnorfeil FM, Brocker T. MicroRNAs regulate dendritic cell differentiation and function[J].J Immunol, 2011, 187(8):3911-3917.
[2]
Sayed D, Abdellatif M. MicroRNAs in development and disease[J]. Physiol Rev, 2011, 91(3):827-887.
[3]
Lu J, Getz G, Miska EA, et al. MicroRNA expression profiles classify human cancers[J]. Nature, 2005, 435:834-838.
[4]
Esquela-Kerscher A, Slack FJ. Oncomirs-microRNAs with a role in cancer[J]. Nat Rev Cancer, 2006, 6:259-269.
[5]
Zhang W, Dahlberg JE, Tam W. MicroRNAs in tumorigenesis:A primer[J]. Am J Pathol, 2007, 171:728-738.
[6]
Cimmino A, Calin GA, Fabbri M, et al.miR-15 and miR-16 induce apoptosis by targeting BCL2[J].Proc Natl Acad Sci USA, 2005, 102(39):13944-13949.
[7]
Kaddar T, Chien WW, Bertrand Y, et al. Prognostic value of miR-16 expression in childhood acute lymphoblastic leukemia relationships to normal and malignant lymphocyte proliferation[J].Leuk Res, 2009, 33(9):1217-1223.
[8]
Schmittgen TD, Livak KJ. Analyzing real-time PCR data by the comparative C (T) method[J].Nat Protoc, 2008, 3(6):1101-1108.
[9]
Schuler D, Szende B. Apoptosis in acute leukemia[J]. Leuk Res, 2004, 28(7):661-666.
[10]
Bonci D, Coppola V, Musumeci M, et al. The miR-15 miR-16-1 cluster controls prostate cancer by targeting multiple oncogenic activities[J]. Nat Med, 2008, 14:1271-1277.
[11]
Calin GA, Cimmino A, Fabbri M, et al. MiR-15a and miR-16-1 cluster functions in human leukemia[J]. Proc Natl Acad Sci USA, 2008, 105:5166-5171.
[12]
Jing Q, Huang S, Guth S, et al. Involvement of microRNA in AU-rich element-mediated mRNA instability[J]. Cell, 2005, 20:623-634.
[13]
Aqeilan RI, Calin GA, Croce CM.miR-15a and miR-16-1 in cancer: Discovery, function and future perspectives[J].Cell Death Different, 2010, 17:215-220.
[14]
Dejean E, Renalier MH, Foisseau M, et al.Hypoxia-microRNA-16 downregulation induces VEGF expression in anaplastic lymphoma kinase (ALK)-positive anaplastic large-cell lymphomas[J].Leukemia, 2011, 25(12):1882-1890.
[1] 张璇, 马宇童, 苗玉倩, 张云, 吴士文, 党晓楚, 陈颖颖, 钟兆明, 王雪娟, 胡淼, 孙岩峰, 马秀珠, 吕发勤, 寇海燕. 超声对Duchenne肌营养不良儿童膈肌功能的评价[J]. 中华医学超声杂志(电子版), 2023, 20(10): 1068-1073.
[2] 张宝富, 俞劲, 叶菁菁, 俞建根, 马晓辉, 刘喜旺. 先天性原发隔异位型肺静脉异位引流的超声心动图诊断[J]. 中华医学超声杂志(电子版), 2023, 20(10): 1074-1080.
[3] 韩丹, 王婷, 肖欢, 朱丽容, 陈镜宇, 唐毅. 超声造影与增强CT对儿童肝脏良恶性病变诊断价值的对比分析[J]. 中华医学超声杂志(电子版), 2023, 20(09): 939-944.
[4] 刘婷婷, 林妍冰, 汪珊, 陈幕荣, 唐子鉴, 代东伶, 夏焙. 超声衰减参数成像评价儿童代谢相关脂肪性肝病的价值[J]. 中华医学超声杂志(电子版), 2023, 20(08): 787-794.
[5] 周钰菡, 肖欢, 唐毅, 杨春江, 周娟, 朱丽容, 徐娟, 牟芳婷. 超声对儿童髋关节暂时性滑膜炎的诊断价值[J]. 中华医学超声杂志(电子版), 2023, 20(08): 795-800.
[6] 米洁, 陈晨, 李佳玲, 裴海娜, 张恒博, 李飞, 李东杰. 儿童头面部外伤特点分析[J]. 中华损伤与修复杂志(电子版), 2023, 18(06): 511-515.
[7] 中华医学会烧伤外科学分会小儿烧伤学组. 儿童烧伤早期休克液体复苏专家共识(2023版)[J]. 中华损伤与修复杂志(电子版), 2023, 18(05): 371-376.
[8] 王蕾, 王少华, 牛海珍, 尹腾飞. 儿童腹股沟疝围手术期风险预警干预[J]. 中华疝和腹壁外科杂志(电子版), 2023, 17(06): 768-772.
[9] 李芳, 许瑞, 李洋洋, 石秀全. 循证医学理念在儿童腹股沟疝患者中的应用[J]. 中华疝和腹壁外科杂志(电子版), 2023, 17(06): 782-786.
[10] 闵筱兰, 周洁超, 陈振添. 健康管理联合心理干预用于腹腔镜腹股沟疝手术患儿术后效果观察[J]. 中华疝和腹壁外科杂志(电子版), 2023, 17(05): 657-661.
[11] 吕垒, 冯啸, 何凯明, 曾凯宁, 杨卿, 吕海金, 易慧敏, 易述红, 杨扬, 傅斌生. 改良金氏评分在儿童肝豆状核变性急性肝衰竭肝移植手术时机评估中价值并文献复习[J]. 中华肝脏外科手术学电子杂志, 2023, 12(06): 661-668.
[12] 卓少宏, 林秀玲, 周翠梅, 熊卫莲, 马兴灶. CD64指数、SAA/CRP、PCT联合检测在小儿消化道感染性疾病鉴别诊断中的应用[J]. 中华消化病与影像杂志(电子版), 2023, 13(06): 505-509.
[13] 刘笑笑, 张小杉, 刘群, 马岚, 段莎莎, 施依璐, 张敏洁, 王雅晳. 中国学龄前儿童先天性心脏病流行病学研究进展[J]. 中华临床医师杂志(电子版), 2023, 17(9): 1021-1024.
[14] 李静, 张玲玲, 邢伟. 兴趣诱导理念用于小儿手术麻醉诱导前的价值及其对家属满意度的影响[J]. 中华临床医师杂志(电子版), 2023, 17(07): 812-817.
[15] 余林阳, 王美英, 李建斌, 楼骁斌, 谢思远, 马志忠, 齐海英, 李稼. 高原地区肺炎合并右心功能衰竭体征患儿的肺动脉压力和心脏形态与功能的特征[J]. 中华临床医师杂志(电子版), 2023, 17(05): 535-544.
阅读次数
全文


摘要