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14株伴有11q23易位的白血病和淋巴瘤细胞系的表型与基因型特征分析

Phenotypic and genotypic characterization of 14 leukemia and lymphoma cell lines with 11q23 translocations.

作者信息

Iida S, Saito M, Okazaki T, Seto M, Yamamoto K, Akao Y, Ogura M, Suzuki H, Ariyoshi Y, Koike K

机构信息

Department of Hematology and Chemotherapy, Aichi Cancer Center, Japan.

出版信息

Leuk Res. 1992 Dec;16(12):1155-63. doi: 10.1016/0145-2126(92)90113-l.

DOI:10.1016/0145-2126(92)90113-l
PMID:1465024
Abstract

11q23 translocation is the most popular chromosomal abnormality in infant leukemia. In adults, it is often encountered in non-Hodgkin's lymphoma (NHL). In this study, we analyzed the phenotypic and genotypic characteristics of 9 acute leukemic cell lines with 11q23 translocations and one with deletion of the 11q23 locus, nine of which were established by researchers in this group, together with 4 NHL cell lines with 11q23 translocations. All lines were considered to belong to the B-cell lineage at different stages. All 10 leukemic lines showed clonal rearrangement of the immunoglobulin heavy chain (IgH) gene: two corresponded to the B-precursor stage (CD19+, cytoplasmic mu-), while the other 8 corresponded to the pre-B stage (cytoplasmic mu+). All 4 NHL lines showed rearrangements of both the IgH and Ig kappa genes with three expressing surface Ig; specifically, mature B-cell phenotype. As for myelocytic-monocytic markers, at least one out of 4 antigens examined were positive in 8 of the 10 leukemic cell lines, while only one of the 4 NHL lines was reactive. There were essentially no clear phenotypic or genotypic differences between t(4;11) and t(11;19) cell lines, supporting the view that both diseases have similar clinicopathological characteristics. These cell lines are also valuable for cloning genes at the chromosomal breakpoints.

摘要

11q23易位是婴儿白血病中最常见的染色体异常。在成人中,它常出现在非霍奇金淋巴瘤(NHL)中。在本研究中,我们分析了9个具有11q23易位的急性白血病细胞系和1个具有11q23位点缺失的细胞系的表型和基因型特征,其中9个是由本研究团队的研究人员建立的,同时分析了4个具有11q23易位的NHL细胞系。所有细胞系均被认为属于不同阶段的B细胞谱系。所有10个白血病细胞系均显示免疫球蛋白重链(IgH)基因的克隆性重排:2个对应B前体细胞阶段(CD19 +,胞质μ-),而另外8个对应前B细胞阶段(胞质μ+)。所有4个NHL细胞系均显示IgH和Igκ基因的重排,其中3个表达表面Ig;具体而言,为成熟B细胞表型。至于髓细胞-单核细胞标志物,在10个白血病细胞系中的8个中,所检测的4种抗原中至少有一种呈阳性,而4个NHL细胞系中只有一个有反应。t(4;11)和t(11;19)细胞系之间基本上没有明显的表型或基因型差异,这支持了两种疾病具有相似临床病理特征的观点。这些细胞系对于在染色体断点处克隆基因也很有价值。

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Molecular cloning of 19p13 breakpoint region in infantile leukemia with t(11;19)(q23;p13) translocation.
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Jpn J Cancer Res. 1993 May;84(5):532-7. doi: 10.1111/j.1349-7006.1993.tb00172.x.