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作 者:李化梅[1] 李龙萍 苏俊[3] 喻安孝[4] 邓飞[5]
机构地区:[1]遵义医药高等专科学校病理教研室,贵州省563002 [2]贵阳市第五人民医院病理科 [3]遵义医学院附属医院病理科 [4]遵义医学院法医教研室 [5]遵义医学院
出 处:《中华临床医师杂志(电子版)》2013年第10期50-52,共3页Chinese Journal of Clinicians(Electronic Edition)
基 金:国家自然科学基金(30160030)
摘 要:目的研究bcl-2/IgH基因重排与微卫星DNA改变在B细胞淋巴瘤发生发展中的作用以及bcl-2/IgH基因重排与微卫星不稳定和杂合性缺失之间的关系。方法应用巢式PCR方法检测bcl-2/IgH基因重排;选取14号染色体上2个微卫星多态性标记,采用聚合酶链反应-单链构象多态性分析法(PCR-SSCP)检测37例B细胞淋巴瘤中微卫星不稳定和杂合性缺失。结果 37例B细胞淋巴瘤中,bcl-2/IgH基因重排频率为24.3%(9/37);微卫星不稳定发生率为48.6%(18/37),杂合性缺失发生率为40.5%(15/37),其中D14S65位点微卫星不稳定和杂合性缺失频率较高,分别为29.7%(11/37)和27%(10/37)。经统计学分析结果显示:D14S65位点bcl-2/IgH基因重排与微卫星不稳定有关(P<0.05),与杂合性缺失无关(P>0.05);但D14S45位点bcl-2/IgH基因重排与微卫星不稳定和杂合性缺失无关(P>0.05)。结论 D14S65是B细胞淋巴瘤中敏感的检测位点,bcl-2/IgH基因重排和微卫星不稳定性可能共同导致B细胞淋巴瘤的发生。Objective To evaluate the role of bcl-2 gene rearrangement and microsatellite DNA alteration in pathogenesis of B-cell lymphoma, and to discuss the relationship of bcl-2/IgH gene rearrangement with microsatellite instability and loss of heterozygosity. Methods Thirty-seven cases of B-cell lymphoma were studied for bd-2 gene rearrangement with nested-PCR method;two microsatellite makers located at chromosome 14 were selected to detected microsatellite alterations (MSI and LOH )by single-strand conformation polymorphism (PCR-SSCP). Results Rearrangement rate of bcl-2 gene was 24. 3 % (9/37) in 37 B-cell lymphoma cases ; Positive rate of MSI was 48.6% (18/37) ,while positive rate of LOH was 40. 5% (15/37). The high frequency of MSIZLOH was at locus of D14S65 (29.7% ,27% ). Bcl-2/IgH gene rearrangement was correlated with MSI at D14S65 (P 〈 0. 05 ), while no correlation was found between MSI or LOH and bcl-2/IgH gene rearrangement at D14S45 (P 〉 0. 05 ). Conclusion D14S65 is sensitive microsatellite loci in B-cell lymphoma, bcl-2/IgH gene rearrangement and MSI might play a role in pathogenesis of B-cell lymphoma.
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