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API2-MALT1 Fusion Transcripts Involved in Mucosa-Associated Lymphoid Tissue Lymphoma : Multiplex RT-PCR Detection Using Formalin-Fixed Paraffin-Embedded Specimens

机译:参与粘膜相关淋巴组织淋巴瘤的API2-MALT1融合转录本:使用福尔马林固定石蜡包埋标本的多重RT-PCR检测

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摘要

Malignant lymphoma of mucosa-associated lymphoid tissue (MALT) type is a distinct clinicopathological disease entity in the category of extranodal marginal zone B-cell lymphoma. Recently, we and others have shown that the API2 gene on chromosome 11 and the MALT1 gene on chromosome 18 are fused as a result of t(11;18)(q21;q21) in MALT lymphomas. Here we report a detection assay that can be used for formalin-fixed, paraffin-embedded specimens. It consists of a multiplex one-tube reverse transcriptase-polymerase chain reaction (RT-PCR) followed by three parallel multiplex nested polymerase chain reactions. Eight variants of the fusion transcripts have been reported to date. When these variants were used as positive controls, all were successfully detected. The subsequent direct sequencing confirmed the results. Using this rapid and simple method, we could detect API2-MALT1 fusion transcripts in 5 of 15 (33%) archival cases of MALT lymphoma for a frequency comparable with those of RT-PCR assays using frozen materials. The lung was the preferential anatomical site of origin of MALT lymphomas harboring API2-MALT1 fusion. No fusion transcript was detected in any of 20 high-grade B-cell lymphomas. Our multiplex RT-PCR assay, which can be used for routinely-processed paraffin samples, should serve as a useful molecular tool for clarifying the clinicopathological significance of API2-MALT1 fusion in MALT lymphoma.
机译:粘膜相关淋巴样组织(sALT)型的恶性淋巴瘤是结外边缘区B细胞淋巴瘤的一种 类型。最近,我们和 的研究表明,t(11; 18)(q21;)使11号染色体上的API2基因与18号染色体上的 MALT1基因融合。 q21) 在MALT淋巴瘤中。在这里,我们报告了一种可用于福尔马林固定石蜡包埋标本的检测分析方法,该方法可 。它由多重单管逆转录聚合酶 链反应(RT-PCR),然后是三个平行的多重 嵌套聚合酶链反应组成。迄今为止,已经报道了融合 转录本的八个变体。将这些变体 用作阳性对照时,都可以成功检测到所有变种。 随后的直接测序证实了结果。使用 这种快速,简单的方法,我们可以在15个(33%)的MALT淋巴瘤 档案病例中的5个(33%)中检测API2-MALT1融合 转录本与使用 冷冻材料进行RT-PCR分析的频率相当。肺是携带API2-MALT1融合蛋白的MALT淋巴瘤的优先解剖部位 。在20个高级B细胞 淋巴瘤中,未检测到 融合转录本。我们的多重RT-PCR分析可用于 常规处理的石蜡样品,应作为有用的 分子工具来阐明临床病理学意义 API2-MALT1在MALT淋巴瘤中的融合。

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  • 来源
    《American Journal of Pathology》 |2001年第2期|699-706|共8页
  • 作者单位

    From the Departments of Pathology,Nagoya City University Medical School, Nagoya;

    From the Departments of Pathology,Nagoya City University Medical School, Nagoya;

    the Laboratory of Chemotherapy,Aichi Cancer Center Research Institute, Nagoya;

    and the Department of Pathology and Clinical Laboratories,Aichi Cancer Center Hospital, Nagoya, Japan;

    and Medicine,Nagoya City University Medical School, Nagoya;

    From the Departments of Pathology,Nagoya City University Medical School, Nagoya;

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