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一例伴有c-myc和TcR-α链基因座重排的T细胞白血病(L1-ALL)中的t(8;14)(q24;q11)易位。

A t(8;14)(q24;q11) translocation in a T-cell leukemia (L1-ALL) with c-myc and TcR-alpha chain locus rearrangements.

作者信息

Mathieu-Mahul D, Sigaux F, Zhu C, Bernheim A, Mauchauffe M, Daniel M T, Berger R, Larsen C J

出版信息

Int J Cancer. 1986 Dec 15;38(6):835-40. doi: 10.1002/ijc.2910380609.

Abstract

Cell lines established from T-cell leukemias have recently been reported to exhibit a chromosome translocation t(8;14) involving proto-oncogene c-myc and the gene of the T-cell receptor alpha-chain(TcR-alpha). In this work, we have studied a case of T-cell leukemia presenting a t(8;14)(q24;q11) translocation that was found in fresh leukemic cells taken during relapse, but was absent in cells collected at diagnosis. Hybridization analysis showed that the breakpoint on chromosome 8 was located 3' to the c-myc exon 3. A TcR-alpha-specific original probe (D14S7, Mathieu-Mahul et al., 1985) revealed two differently rearranged patterns in DNA from leukemic cells obtained at diagnosis and during relapse. In contrast, the rearranged TcR-beta-gene DNA pattern did not change during the course of the disease, indicating that leukemic cells were clonally related. These data indicate that the chromosome breakpoint in 14q11 is situated in the TcR-alpha locus. These results suggest that translocations t(8;14) involving TcR-alpha and c-myc genes in T-cell malignancies are analogous to variant t(2;8) and t(8;22) translocations observed in Burkitt lymphoma. They also establish that the same types of molecular rearrangements due to a t(8;14)(q24;q11) translocation, at first described in T-cell lines established in culture, also exist in vivo and may play a role in the evolution of the leukemic process.

摘要

最近有报道称,从T细胞白血病建立的细胞系表现出涉及原癌基因c-myc和T细胞受体α链(TcR-α)基因的染色体易位t(8;14)。在这项研究中,我们研究了一例T细胞白血病病例,该病例呈现t(8;14)(q24;q11)易位,此易位在复发时采集的新鲜白血病细胞中被发现,但在诊断时采集的细胞中不存在。杂交分析表明,8号染色体上的断点位于c-myc外显子3的3'端。一个TcR-α特异性原始探针(D14S7,Mathieu-Mahul等人,1985年)在诊断时和复发时获得的白血病细胞DNA中显示出两种不同的重排模式。相比之下,重排的TcR-β基因DNA模式在疾病过程中没有改变,表明白血病细胞是克隆相关的。这些数据表明14q11中的染色体断点位于TcR-α基因座。这些结果表明,T细胞恶性肿瘤中涉及TcR-α和c-myc基因的易位t(8;14)类似于在伯基特淋巴瘤中观察到的变异易位t(2;8)和t(8;22)。它们还证实,最初在培养中建立的T细胞系中描述的由于t(8;14)(q24;q11)易位导致的相同类型的分子重排也存在于体内,并且可能在白血病过程的演变中起作用。

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