首页> 外文OA文献 >Mucosa-Associated Lymphoid Tissue Lymphomas with t(11;18)(q21;q21) and Mucosa-Associated Lymphoid Tissue Lymphomas with Aneuploidy Develop Along Different Pathogenetic Pathways
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Mucosa-Associated Lymphoid Tissue Lymphomas with t(11;18)(q21;q21) and Mucosa-Associated Lymphoid Tissue Lymphomas with Aneuploidy Develop Along Different Pathogenetic Pathways

机译:t(11; 18)(q21; q21)的黏膜相关淋巴组织淋巴瘤和非整倍体的黏膜相关淋巴组织淋巴瘤沿着不同的发病途径发展。

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摘要

t(11;18)(q21;q21) and aneuploidy are recurrent chromosomal aberrations in mucosa-associated lymphoid tissue (MALT) lymphomas. To investigate their relationship and clinical significance, we developed a two-color fluorescence in situ hybridization (FISH) technique to detect t(11;18) and aneuploidy in nuclei isolated from paraffin-embedded tissue. Thirty-seven MALT lymphomas (all previously evaluated for t(11;18) by reverse transcriptase-polymerase chain reaction), 1 large cell lymphoma (LCL) arising subsequent to MALT lymphoma, and 16 controls were tested by FISH using the t(11;18) probe set and multiple centromeric probes. t(11;18)(q21;q21) was present by FISH in 11 of 12 polymerase chain reaction-positive MALT lymphomas (92%). The LCL and its clonally identical antecedent MALT lymphoma both showed t(11;18). The LCL had trisomy 12, and a small subset of MALT lymphoma cells had trisomy 3 and/or 12. Only one other MALT lymphoma with t(11;18) showed aneuploidy (trisomy 3) in a small clone, whereas 15 of 25 t(11;18)-negative MALT lymphomas (60%) showed trisomy of chromosomes 18 (n = 12), 3 (n = 8), 7 (n = 2), and/or 11 (n = 1). t(11;18) and aneuploidy are primarily mutually exclusive events, suggesting different pathogenetic pathways in the development of MALT lymphomas. Both t(11;18) and aneuploidy were seen disproportionately in lung, and both were associated with recurrent disease.
机译:t(11; 18)(q21; q21)和非整倍性是与粘膜相关的淋巴样组织(MALT)淋巴瘤的复发性染色体畸变。为了研究它们之间的关系和临床意义,我们开发了一种双色荧光原位杂交(FISH)技术来检测从石蜡包埋的组织中分离出的细胞核中的t(11; 18)和非整倍性。 37例MALT淋巴瘤(以前均通过逆转录酶-聚合酶链反应评估了t(11; 18)),1例MALT淋巴瘤后继发的大细胞淋巴瘤(LCL),以及16例对照通过FISH使用t(11 ; 18)探针组和多个着丝粒探针。 FISH在12个聚合酶链反应阳性MALT淋巴瘤中有11个存在t(11; 18)(q21; q21)(92%)。 LCL及其克隆相同的先前MALT淋巴瘤均显示t(11; 18)。 LCL具有12三体性,一小部分MALT淋巴瘤细胞具有3三体性和/或12三体性。只有一个t(11; 18)的MALT淋巴瘤在一个小克隆中显示非整倍性(3三体性),而25 t中的15 (11; 18)阴性的MALT淋巴瘤(60%)显示三号染色体18(n = 12),3(n = 8),7(n = 2)和/或11(n = 1)。 t(11; 18)和非整倍性主要是相互排斥的事件,表明在MALT淋巴瘤的发生过程中存在不同的致病途径。在肺中t(11; 18)和非整倍性均不成比例,并且都与复发性疾病相关。

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