The molecular analyses of hematological malignancies--lineage specific classification and its clinical implications.

K Kawa-Ha, A Tawa, K Yumura-Yagi, J Hara
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Abstract

Cells from 203 children with leukemia/lymphoma were analyzed by the FAB (French-American-British) system using a broad panel of markers such as immunological marker studies, Southern blot and Northern blot analyses to establish a lineage specific classification of childhood leukemia. Phenotypically, they were divided into B-lineage (62.6%), T-lineage (9.8%), non-lymphoid (14.3%) and uncertain lineage (13.3%). Two B-lineage ALL cells and two T-lineage ALL cells studied did not show immunoglobulin (Ig) or T-cell receptor (TCR) gene rearrangements, respectively. Therefore, those four cases were excluded from the final classification. The uncertain lineage leukemia, which includes undifferentiated leukemia and mixed lineage leukemia, were further subclassified at the DNA and RNA levels. The definitions of B-lineage and T-lineage cells, incidence of dual genotypes or spillover, heterogeneity of undifferentiated leukemia, and a new classification for mixed lineage leukemia were discussed.

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血液系统恶性肿瘤的分子分析——谱系特异性分类及其临床意义。
来自203名白血病/淋巴瘤儿童的细胞通过FAB(法国-美国-英国)系统进行分析,使用广泛的标记,如免疫标记研究、Southern blot和Northern blot分析,以建立儿童白血病的谱系特异性分类。表型上分为b系(62.6%)、t系(9.8%)、非淋巴系(14.3%)和不确定系(13.3%)。研究的两个b系ALL细胞和两个t系ALL细胞分别未显示免疫球蛋白(Ig)或t细胞受体(TCR)基因重排。因此,这4例被排除在最终分类之外。不确定谱系白血病包括未分化白血病和混合谱系白血病,在DNA和RNA水平上进一步细分。本文讨论了b系和t系细胞的定义、双基因型或外溢的发生率、未分化白血病的异质性以及混合系白血病的新分类。
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