您的位置: 专家智库 > >

国家自然科学基金(30400529)

作品数:3 被引量:6H指数:2
相关作者:汤立军王建军洪丽萍更多>>
相关机构:中南大学更多>>
发文基金:国家自然科学基金湖南省自然科学杰出青年基金更多>>
相关领域:医药卫生更多>>

文献类型

  • 2篇中文期刊文章

领域

  • 2篇医药卫生

主题

  • 1篇白血
  • 1篇白血病
  • 1篇MULTIP...
  • 1篇EXPRES...
  • 1篇GENE_E...
  • 1篇HUMAN
  • 1篇MIRNA

机构

  • 1篇中南大学

作者

  • 1篇王建军
  • 1篇汤立军

传媒

  • 1篇生命科学研究
  • 1篇Chines...

年份

  • 1篇2011
  • 1篇2007
3 条 记 录,以下是 1-2
排序方式:
miRNA在白血病中的研究进展被引量:3
2011年
microRNA(miRNA)是一种小分子非编码RNA,在细胞增殖、分化和凋亡等多种生理过程中发挥着重要作用.白血病相关miRNA研究进展迅速,并呈现了miRNA介导白血病瘤细胞增殖、分化和凋亡的调控网络.深入了解相关miRNA与白血病的发生、发展关系将为白血病的治疗开辟新途径.
王建军汤立军
关键词:MIRNA白血病
Molecular features and expression of DAZAP2 in human multiple myeloma被引量:2
2007年
Background In our previous study, we found that DAZAP2 was the most significantly down regulated gene when differential screening of complementary DNA (cDNA) chips were used to analyze mRNA isolated from bone marrow mononuclear cells from newly diagnosed multiple myeloma (MM) patients without anticancer treatment. In this study, we observed DAZAP2 mRNA and protein expression in the mononuclear cells from MM bone marrow and investigated its role in the pathogenesis of MM. Methods The full-length cDNA of DAZAP2 was cloned and sequenced from mononuclear cells from human bone marrow. The nucleotide and amino acid sequences of DAZAP2 were analyzed using the ClustalW program. A dendrogram was constructed by multiple sequence alignment using ClustalW and amino acid sequence identity/similarity was derived based on comparisons attained using the MegAlign software. The recombinant pEGFP expression vector was constructed and the confocal microscopy was used for the localization of the DAZAP2 protein in transfected COS7 cells. The expression of DAZAP2 mRNA was detected by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) and the expression level of DAZAP2 protein was detected by Western blotting analysis in MM samples. Results DAZAP2 proteins of vertebrates is highly conserved in evolution. It contains a proline-rich region, several potential SH2 and SH3 domain-binding motifs and a possible protein kinase C (PKC) phosphorylation site. We showed by confocal microscopy that the DAZAP2 protein predominantly resides in the cytoplasm with a discrete pattern of punctuated distribution. The expression of DAZAP2 was not detected in 24 of 36 MM samples by semi-quantitative RT-PCR. In contrast, DAZAP2 expression was detected in all 30 normal controls. The expression level of DAZAP2 protein was assayed by Western blotting analysis, showing a robust down-regulation in MM patients (P〈0.001) that matched with the results of the RT-PCR. Conclusions DAZAP2 is downregulated in MM samples and it
SHI Yi-wuSHEN RongREN WeiTANG Li-junTAN Da-renHU Wei-xin
共1页<1>
聚类工具0