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伴有7号染色体q34带重排的T细胞肿瘤的临床与生物学特征

Clinical and biologic characterization of T-cell neoplasias with rearrangements of chromosome 7 band q34.

作者信息

Smith S D, Morgan R, Gemmell R, Amylon M D, Link M P, Linker C, Hecht B K, Warnke R, Glader B E, Hecht F

机构信息

Department of Pediatrics and Pathology, Stanford University School of Medicine, CA.

出版信息

Blood. 1988 Feb;71(2):395-402.

PMID:2962650
Abstract

In T cell malignancy, rearrangements of chromosome 14 have been observed with a break in the band that contains the alpha chain gene for the T cell receptor (TCR). Because the beta chain TCR gene is in chromosome band 7q34, we searched for and report finding specific rearrangements of 7q34 exclusively in T cell malignancies. The rearrangements were reciprocal translocations between 7q34 and other points: 1p34, 9q32, 9q34, 15q22, and 19p13. The malignancies containing a 7q34 translocation were either T cell acute lymphoblastic leukemias or T cell lymphoblastic lymphomas that had similarities in clinical, enzyme, immunologic, and cellular characteristics. Hybridization using a probe to the beta-TCR gene disclosed unique rearrangements consistent with clonality in every case. A common pattern with chromosome breakpoints involving TCR genes may be emerging in T cell neoplasia.

摘要

在T细胞恶性肿瘤中,已观察到14号染色体重排,其断裂发生在包含T细胞受体(TCR)α链基因的条带中。由于β链TCR基因位于7号染色体带7q34,我们进行了搜索并报告发现仅在T细胞恶性肿瘤中存在7q34的特定重排。这些重排是7q34与其他位点之间的相互易位:1p34、9q32、9q34、15q22和19p13。含有7q34易位的恶性肿瘤要么是T细胞急性淋巴细胞白血病,要么是T细胞淋巴母细胞淋巴瘤,它们在临床、酶学、免疫学和细胞特征方面具有相似性。使用β-TCR基因探针进行杂交显示,在每种情况下均存在与克隆性一致的独特重排。涉及TCR基因的染色体断点的常见模式可能正在T细胞肿瘤形成中出现。

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