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凋亡抑制基因API2和一个新的18q基因MLT,在与黏膜相关淋巴组织淋巴瘤相关的t(11;18)(q21;q21)中经常发生重排。

The apoptosis inhibitor gene API2 and a novel 18q gene, MLT, are recurrently rearranged in the t(11;18)(q21;q21) associated with mucosa-associated lymphoid tissue lymphomas.

作者信息

Dierlamm J, Baens M, Wlodarska I, Stefanova-Ouzounova M, Hernandez J M, Hossfeld D K, De Wolf-Peeters C, Hagemeijer A, Van den Berghe H, Marynen P

机构信息

Department of Oncology and Hematology, University Hospital Eppendorf, Hamburg, Germany.

出版信息

Blood. 1999 Jun 1;93(11):3601-9.

Abstract

Marginal zone cell lymphomas of the mucosa-associated lymphoid tissue (MALT) are the most common subtype of lymphoma arising at extranodal sites. The t(11;18)(q21;q21) appears to be the key genetic lesion and is found in approximately 50% of cytogenetically abnormal low-grade MALT lymphomas. We show that the API2 gene, encoding an inhibitor of apoptosis also known as c-IAP2, HIAP1, and MIHC, and a novel gene on 18q21 characterized by several Ig-like C2-type domains, named MLT, are recurrently rearranged in the t(11;18). In both MALT lymphomas analyzed, the breakpoint in API2 occurred in the intron separating the exons coding respectively for the baculovirus IAP repeat domains and the caspase recruitment domain. The breakpoints within MLT differed but the open reading frame was conserved in both cases. In one case, the translocation was accompanied by a cryptic deletion involving the 3' part of API2. As a result, the reciprocal transcript was not present, strongly suggesting that the API2-MLT fusion is involved in the oncogenesis of MALT lymphoma.

摘要

黏膜相关淋巴组织(MALT)边缘区细胞淋巴瘤是最常见的结外淋巴瘤亚型。t(11;18)(q21;q21)似乎是关键的基因病变,约50%细胞遗传学异常的低级别MALT淋巴瘤中可发现该病变。我们发现,编码凋亡抑制因子(也称为c-IAP2、HIAP1和MIHC)的API2基因以及18q21上一个以几个Ig样C2型结构域为特征的新基因(命名为MLT)在t(11;18)中经常发生重排。在分析的两例MALT淋巴瘤中,API2的断点发生在分别编码杆状病毒IAP重复结构域和半胱天冬酶募集结构域的外显子之间的内含子中。MLT内的断点不同,但两种情况下开放阅读框均保守。在一例中,易位伴有涉及API2 3'部分的隐匿性缺失。结果,反向转录本不存在,强烈提示API2-MLT融合参与了MALT淋巴瘤的肿瘤发生。

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