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从一名弥漫性大B细胞淋巴瘤患者的腹水中建立携带t(1;14)(q21;q32)易位的人细胞系(SKI-DLCL-1)。

Establishment of a human cell line (SKI-DLCL-1) with a t(1;14)(q21;q32) translocation from the ascites of a patient with diffuse large cell lymphoma.

作者信息

Goy A, Gilles F, Remache Y, Filippa D, Portlock C S, Jhanwar S C, Zelenetz A D

机构信息

Department of Medicine, Memorial Hospital, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

Leuk Lymphoma. 2001 Jan;40(3-4):419-23. doi: 10.3109/10428190109057942.

Abstract

Cytogenetic abnormalities at chromosome 1q21 are among the most common second genetic events observed in Non-Hodgkin's Lymphomas and have prognostic significance. Recently, BCL9 has been cloned from a pre-B-cell lymphoblastic leukemia cell line, which carried a t(1:14)(q21;q32). However, among a panel of 39 B-cell malignancies with 1q21 translocation, only two cases showed rearrangement for the BCL9 gene. We report the establishment of a new lymphoma cell line from a patient with relapsed diffuse large cell lymphoma. This cell line SKI-DLCL-1 showed cell surface antigens identical to the original tumor and demonstrated the profile of a mature B-cell phenotype: CD19 and CD20 positive, CD5 and C10 negative. It carried a t(1;14)(q21;q32) translocation identical to the original tumor. Although the clinical presentation was an isolated effusion lymphoma, studies for HIV-1, HHV8 and EBV were all negative. Southern blot analysis demonstrated that BCL9 was not rearranged in the SKI-DLCL-1 cell line. In addition, the BCL9 gene was not over-expressed in SKI-DLCL-1 cell line. The identification of a new locus at 1q21 will help clarify the pathogenesis of B-cell malignancies with a translocation involving this locus.

摘要

1q21染色体的细胞遗传学异常是在非霍奇金淋巴瘤中观察到的最常见的第二种遗传事件,具有预后意义。最近,BCL9已从一个携带t(1;14)(q21;q32)的前B淋巴细胞白血病细胞系中克隆出来。然而,在一组39例伴有1q21易位的B细胞恶性肿瘤中,只有2例显示BCL9基因重排。我们报告了从一名复发性弥漫性大细胞淋巴瘤患者建立了一种新的淋巴瘤细胞系。该细胞系SKI-DLCL-1显示出与原始肿瘤相同的细胞表面抗原,并表现出成熟B细胞表型的特征:CD19和CD20阳性,CD5和C10阴性。它携带与原始肿瘤相同的t(1;14)(q21;q32)易位。尽管临床表现为孤立性浆膜腔淋巴瘤,但对HIV-1、HHV8和EBV的检测均为阴性。Southern印迹分析表明,SKI-DLCL-1细胞系中BCL9没有重排。此外,BCL9基因在SKI-DLCL-1细胞系中没有过度表达。鉴定1q21处的一个新位点将有助于阐明涉及该位点易位的B细胞恶性肿瘤的发病机制。

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