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NB4,一种从人类急性早幼粒细胞白血病(M3)中分离出的带有t(15;17)标记的成熟诱导细胞系。

NB4, a maturation inducible cell line with t(15;17) marker isolated from a human acute promyelocytic leukemia (M3).

作者信息

Lanotte M, Martin-Thouvenin V, Najman S, Balerini P, Valensi F, Berger R

机构信息

INSERM U-301, SDI No 15954.1 CNRS, Centre Hayem, Paris, France.

出版信息

Blood. 1991 Mar 1;77(5):1080-6.

PMID:1995093
Abstract

Acute promyelocytic leukemia (APL) is a well-defined entity among acute leukemia, cytogenetically characterized by a t(15;17) (q22;q11-12) translocation. In vitro and in vivo studies suggest that all-trans retinoic acid (RA) treatment restores cell maturation. We have isolated the first permanent cell line with t(15;17), derived from the marrow of a patient with APL in relapse. The establishment of the cell line, its morphologic, karyotypic, and immunohistochemical features are reported. RA induced cell line maturation. Cells strongly expressed myeloid markers, but also some T-cell markers. Additional karyotypic abnormalities, a 12p rearrangement and the possible presence of a homogeneous staining region (HSR) on 19q+ are discussed both in relation to T-cell (CD2, CD4) and monocyte (CD9) markers, and to the acquired cell growth autonomy. The cell line represents a remarkable tool for biomolecular studies.

摘要

急性早幼粒细胞白血病(APL)是急性白血病中一个明确的实体,细胞遗传学特征为t(15;17)(q22;q11 - 12)易位。体外和体内研究表明,全反式维甲酸(RA)治疗可恢复细胞成熟。我们从一名复发的APL患者的骨髓中分离出了第一株具有t(15;17)的永久性细胞系。本文报道了该细胞系的建立及其形态学、核型和免疫组化特征。RA诱导细胞系成熟。细胞强烈表达髓系标志物,但也表达一些T细胞标志物。本文还讨论了额外的核型异常,即12p重排以及19q+上可能存在的均匀染色区(HSR),这与T细胞(CD2、CD4)和单核细胞(CD9)标志物以及获得性细胞生长自主性有关。该细胞系是生物分子研究的一个重要工具。

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