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Detection of microvesicle miRNA expression in ALL subtypes and analysis of their functional roles
  • 期刊名称:Journal of Huazhong University of Science and Tech
  • 时间:2014.10.16
  • 页码:640-645
  • 分类:Q522[生物学—生物化学] TD456[矿业工程—矿山机电]
  • 作者机构:[1]Center.for Stem Cell Research and Application, Institute ofHematology, Union Hospital, Tongji Medical College, HuazhongUniversity of Science and Technology, Wuhan 430022, China, [2]Neonatal Screening Center, Zhuzhou Women and Children Medical Care Center, Zhuzhou 412000, China
  • 相关基金:This work was supported by the National Natural Science Foundation of China (No. 81170462).
  • 相关项目:CML来源的微泡表达HERGK+通道蛋白调节CML细胞功能及格列卫干预作用
中文摘要:

Microvesicles(MVs) are the heterogeneous mixtures of vesicles. MVs released by leukemia cells constitute an important part of the leukemia microenvironment. MVs might act as important reservoirs of microRNAs(miRNAs). It is worth evaluating whether MVs possess some unique miRNA contents that are valuable in understanding the pathogenesis. In this study, we investigated the miRNA expression patterns of Nalm-6-derived MVs, Jurkat-derived MVs and normal cell-derived MVs using miRNA microarrays. The potential target genes regulated by differentially expressed miRNAs were also predicted and analyzed. Results demonstrated that 182 miRNAs and 166 miRNAs were differentially expressed in Nalm-6-MVs and Jurkat-MVs, respectively. Many oncogenes, tumor suppressors and signal pathway genes were targeted by these aberrantly expressed miRNAs, which might contribute to the development of B-ALL or T-ALL. Our findings expanded the potential diagnostic markers of ALL and provided useful information for ALL pathogenesis.

英文摘要:

Microvesicles (MVs) are the heterogeneous mixtures of vesicles. MVs released by leukemia cells constitute an important part of the leukemia microenvironment. MVs might act as important reser- voirs of microRNAs (miRNAs). It is worth evaluating whether MVs possess some unique miRNA con- tents that are valuable in understanding the pathogenesis. In this study, we investigated the miRNA ex- pression patterns of Nalm-6-derived MVs, Jurkat-derived MVs and normal cell-derived MVs using miRNA microarrays. The potential target genes regulated by differentially expressed miRNAs were also predicted and analyzed. Results demonstrated that 182 miRNAs and 166 miRNAs were differentially expressed in Nalm-6-MVs and Jurkat-MVs, respectively. Many oncogenes, tumor suppressors and sig- nal pathway genes were targeted by these aberrantly expressed miRNAs, which might contribute to the development of B-ALL or T-ALL. Our findings expanded the potential diagnostic markers of ALL and provided useful information for ALL pathogenesis.

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