Down-Regulation of miR-92 in Human Plasma Is a Novel Marker for Acute Leukemia Patients

被引:219
作者
Tanaka, Masami
Oikawa, Kosuke
Takanashi, Masakatsu
Kudo, Motoshige
Ohyashiki, Junko
Ohyashiki, Kazuma
Kuroda, Masahiko
机构
[1] Department of Pathology, Tokyo Medical University, Tokyo
[2] Department of Cell Therapy, Tokyo Medical University, Tokyo
[3] Intractable Disease Therapeutic Research Center, Tokyo Medical University, Tokyo
[4] First Department of Internal Medicine, Tokyo Medical University, Tokyo
[5] First Department of Pathology, Wakayama Medical University, Wakayama
来源
PLOS ONE | 2009年 / 4卷 / 05期
关键词
ACUTE MYELOID-LEUKEMIA; LUNG CANCERS; MICRORNAS; EXPRESSION; EXOSOMES; MIR-17-92; ACCUMULATION; POLYCISTRON; MECHANISM; BEARING;
D O I
10.1371/journal.pone.0005532
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: MicroRNAs are a family of 19- to 25-nucleotides noncoding small RNAs that primarily function as gene regulators. Aberrant microRNA expression has been described for several human malignancies, and this new class of small regulatory RNAs has both oncogenic and tumor suppressor functions. Despite this knowledge, there is little information regarding microRNAs in plasma especially because microRNAs in plasma, if exist, were thought to be digested by RNase. Recent studies, however, have revealed that microRNAs exist and escape digestion in plasma. Methodology/Principal Findings: We performed microRNA microaray to obtain insight into microRNA deregulation in the plasma of a leukemia patient. We have revealed that microRNA-638 (miR-638) is stably present in human plasmas, and microRNA-92a (miR-92a) dramatically decreased in the plasmas of acute leukemia patients. Especially, the ratio of miR-92a/miR-638 in plasma was very useful for distinguishing leukemia patients from healthy body. Conclusions/Significance: The ratio of miR-92a/miR-638 in plasma has strong potential for clinical application as a novel biomarker for detection of leukemia.
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页数:5
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