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艾滋病相关淋巴瘤细胞系的体外建立:表型特征、癌基因和抑癌基因损伤以及爱泼斯坦-巴尔病毒感染的异质性

In vitro establishment of AIDS-related lymphoma cell lines: phenotypic characterization, oncogene and tumor suppressor gene lesions, and heterogeneity in Epstein-Barr virus infection.

作者信息

Gaidano G, Parsa N Z, Tassi V, Della-Latta P, Chaganti R S, Knowles D M, Dalla-Favera R

机构信息

Division of Oncology, Presbyterian Hospital, New York, New York.

出版信息

Leukemia. 1993 Oct;7(10):1621-9.

PMID:8412324
Abstract

Lymphoma represents a major source of morbidity and mortality among AIDS patients. AIDS-associated non-Hodgkin lymphomas (AIDS-NHL) are almost invariably B-cell derived, are classified as high or intermediate grade lymphomas, and display three main histologic types: namely, small non-cleaved cell lymphoma (SNCCL), large cell immunoblastic plasmacytoid lymphoma (LC-IBPL), and large cell lymphoma (LCL). Here we report the in vitro establishment of three new AIDS-NHL cell lines (termed HBL-1, HBL-2, and HBL-3) derived from three AIDS-SNCCL patients differing in primary tumor sites and risk factors for HIV infection. The derivation of the cell lines from the original tumor clones was established by immunophenotypic and molecular genetic analysis. These cell lines display clonal immunoglobulin gene rearrangement, express surface immunoglobulin and B-cell restricted markers, and exhibit a phenotype consistent with SNCCL. Monoclonal Epstein-Barr virus infection was found in only one of the cell lines (HBL-1). Cytogenetic analysis demonstrated the presence of a chromosomal translocation involving the c-myc proto-oncogene and an immunoglobulin locus in all three cell lines. The pattern of genetic lesions detected in HBL-1, HBL-2, and HBL-3 reflects that found in primary AIDS-SNCCL and includes activation of the c-myc oncogene as well as inactivation of the p53 tumor suppressor gene. These cell lines should prove useful in studies of the biological, immunological, and viral factors involved in AIDS-associated lymphomagenesis.

摘要

淋巴瘤是艾滋病患者发病和死亡的主要原因之一。艾滋病相关非霍奇金淋巴瘤(AIDS-NHL)几乎均源自B细胞,被归类为高级别或中级别淋巴瘤,主要有三种组织学类型:即小无裂细胞淋巴瘤(SNCCL)、大细胞免疫母细胞浆细胞样淋巴瘤(LC-IBPL)和大细胞淋巴瘤(LCL)。在此,我们报告从三名原发性肿瘤部位和HIV感染危险因素不同的艾滋病-SNCCL患者中体外建立了三种新的AIDS-NHL细胞系(分别称为HBL-1、HBL-2和HBL-3)。通过免疫表型和分子遗传学分析确定了这些细胞系源自原始肿瘤克隆。这些细胞系显示克隆性免疫球蛋白基因重排,表达表面免疫球蛋白和B细胞限制性标志物,并表现出与SNCCL一致的表型。仅在其中一个细胞系(HBL-1)中发现了单克隆EB病毒感染。细胞遗传学分析表明,所有三个细胞系中均存在涉及c-myc原癌基因和一个免疫球蛋白基因座的染色体易位。在HBL-1、HBL-2和HBL-3中检测到的基因损伤模式反映了原发性艾滋病-SNCCL中的情况,包括c-myc癌基因的激活以及p53肿瘤抑制基因的失活。这些细胞系在研究艾滋病相关淋巴瘤发生过程中涉及的生物学、免疫学和病毒学因素方面应会证明是有用的。

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