• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

临床输血与检验 ›› 2016, Vol. 18 ›› Issue (2): 127-130.DOI: 10.3969/j.issn.1671-2587.2016.02.012

• 临床检验研究 • 上一篇    下一篇

miR-125a-3p在急性髓细胞白血病患者外周血中的表达及其意义*

潘请, 彭静, 孙晓曦, 戴春阳, 马筱玲   

  1. 233030 安徽省蚌埠医学院(潘请); 安徽医科大学附属省立医院检验科(潘请,彭静,孙晓曦,戴春阳,马筱玲)
  • 收稿日期:2015-11-12 出版日期:2016-04-20 发布日期:2016-09-21
  • 通讯作者: 马筱玲,(E-mail)xiaolingma@126.com。
  • 作者简介:潘请(1985-),女,山东菏泽人,检验技师,在读硕士研究生,主要从事细菌耐药性研究,(Tel)15555109193(E-mail)qingqingpan@126.com。
  • 基金资助:
    *本课题受安徽省自然科学基金(No.1408085MH188)资助

The Expression and Significance of MiR-125a-3p in Peripheral Blood of Patients with Acute Myeloid Leukemia

PAN Qing, PENG Jing, SUN Xiao-xi, DAI Chun-yang, MA Xiao-ling, et al   

  1. Bengbu Medical College,Bengbu,Anhui 233030
  • Received:2015-11-12 Online:2016-04-20 Published:2016-09-21

摘要: 目的探讨miR-125a-3p在急性髓细胞白血病( Acute myeloid leukemia,AML)患者外周血中的表达及其意义。方法采用实时荧光定量PCR检测119例AML患者外周血标本中miR-125a-3p的表达水平,其中,初诊组53例,复发组12例,治疗组54例。另选择12例正常人作为对照。随机选择初诊组中7例患者进行外周血miR-125a-3p动态监测。结果与正常对照组比较,初诊组和复发组患者外周血miR-125a-3p的表达水平明显减低,且差异有统计学意义(P < 0.05),而治疗组患者外周血miR-125a-3p的表达水平增高,但差异无统计学意义(P > 0.05)。对初诊组和治疗组中不同FAB分型的AML患者miR-125a-3p的表达水平进行比较,发现初诊组内各型患者之间miR-125a-3p表达的差异无统计学意义(P > 0.05);治疗组内M4型AML患者miR-125a-3p表达明显高于M0 型,差异有统计学意义(P <0.05),其他各型之间miR-125a-3p表达差异无统计学意义(P > 0.05)。7 例患者miR-125a-3p动态监测结果显示,在治疗过程中,miR-125a-3p表达一直维持在较高的水平;1例患者缓解4~5个疗程后复发,其miR-125a-3p表达再次降低。结论miR-125a-3p在AML 初发及复发患者外周血中低表达,诱导治疗后表达量升高,这可能与AML的发生发展有关,miR-125a-3p有望成为AML疗效评价和复发监测的生物学指标。

关键词: miR-125a-3p, 急性髓细胞白血病, 实时荧光定量PCR, 动态监测, 生物学指标

Abstract: ObjectiveThis study was to investigate the expression and significance of miR-125a-3p in peripheral blood of Acute myeloid leukemia patients. MethodsReal-time fluorescent quantitative PCR was performed to detect the expression levels of miR-125a-3p in peripheral blood specimens of 119 AML patients, including 53 newly diagnosed, 12 relapsed and 54 treated patients. In addition, 12 healthy persons were selected as normal controls. Moreover, 7 persons were selected randomly from newly diagnosed patients for dynamic monitoring of miR-125a-3p levels in peripheral blood. ResultsCompared with normal controls, the expression levels of miR-125a-3p were decreased significantly in newly diagnosed and relapsed patients (P<0.05). However, miR-125a-3p expression in treated patients were increased (P> 0.05). The researchers compared respectively the expression levels of miR-125a-3p in different FAB subtypes of newly diagnosed and treated patients and found that there were no significant differences among various subtypes in newly diagnosed patients (P>0.05). In treated patients, the expression of miR-125a-3p in M4 patients was significantly higher than it in M0 (P<0.05), however, the differences between other subtype patients were not significant (P>0.05). Dynamic monitoring of miR-125a-3p levels of 7 patients showed that miR-25a-3p expression maintained a higher level in the process of the treatment; when one patient with remission relapsed after 4~5 courses of treatment, miR-125a-3p expression reduced again. ConclusionThe expression of miR-125a-3p is obviously decreased in patients with newly diagnosed and relapsed AML, and chemotherapy arises the expression level, which may be related with the occurrence and development of AML. Thus miR-125a-3p is expected to become a biological marker of AMLin evaluating for therapy efficacy and monitoring.

Key words: miR-125a-3p, Acute, myeloid, leukemia, Real-time, fluorescence, quantitative, PCR, Dynamic, monitoring, Biological, marker

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