LRP16基因的SAGE谱及其在正常血细胞、白血病细胞中的表达状况

SAGE pattern of LRP16 gene and its expression in normal blood and leukemic cells

  • 摘要: 目的: 通过信息学和实验学的方法检测LRP1 6基因在肿瘤细胞以及在造血发育不同阶段的表达状况,探讨其在肿瘤发生、发展以及在血细胞成熟过程中可能的作用。方法: 以NCBI提供的高通量CGAP SAGEmap数据库为实验对象,“VirtualNorthern”程序为实验工具,分析比较了LRP1 6基因在多种肿瘤组织、细胞系和相应正常组织中的表达谱;采用半定量RT PCR方法检测了该基因在多种正常血细胞及白血病细胞中的表达量。结果: SAGE结果显示LRP1 6在人类多种肿瘤细胞中的表达量明显高于其正常对应组织。脐血中未检测到LRP1 6表达,正常骨髓及经G CSF动员的PBSC (peripheralbloodstemcells)中的表达量明显低于正常人外周血、原代白血病细胞及白血病细胞系(P<0.001)。结论: LRP1 6在不同的血细胞中表达量不同。同时表明LRP1 6与急性白血病等多种肿瘤的发生、发展存在相关性;在初诊与复发白血病中,LRP1 6的表达差异值得进一步研究。

     

    Abstract: Objective: To investigate the possible significance of LRP16during tumor development and progression and during hematopoietic maturation,bioinformatic and experimental method were employed to detect the expression state of LRP16in tumor development and different hematopoietic stages. Methods: Using CGAP/SAGEmap database provided by NCBI as experimental material,"Virtual Northern"program as tool,LRP16expression pattern was compared among multitumor tissues,cell lines and corresponding normal tissues.Sem-i quantified RT-PCR was adopted to compare the expression amount among normal blood cells and leukemic cells. Results: Analysis of SAGE pattern showed that LRP16gene was highly expressed in several human tumor cells than in their normal counterparts.LRP16was not detected in cord blood cells.The expression amount of LRP16gene in normal bone marrow and PBSC(peripheral blood stem cells)mobilized by G-CSF were significantly lower than in normal peripheral blood,primary leukemic cells and leukemic cell lines(P<0.0001)such as HL60,K562 and U937. Conclusion: These results suggested that LRP16have different expression level in different blood cells,and demonstrated that LRP16is related to AL and many kinds of human tumors. The expression difference between diagnostic and relapsed AML is valuable to be further investigated.

     

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