...
首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Breast implant-associated, ALK-negative, T-cell, anaplastic, large-cell lymphoma: establishment and characterization of a model cell line (TLBR-1) for this newly emerging clinical entity.
【24h】

Breast implant-associated, ALK-negative, T-cell, anaplastic, large-cell lymphoma: establishment and characterization of a model cell line (TLBR-1) for this newly emerging clinical entity.

机译:乳房植入物相关,ALK阴性,T细胞,间变性,大细胞淋巴瘤:建立和表征这种新兴临床实体的模型细胞系(TLBR-1)。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: Primary lymphomas of the breast are very rare (0.2-1.5% of breast malignancies) and the vast majority (95%) are of B-cell origin. Recently, 40 cases of clinically indolent anaplastic large-cell kinase (ALK)-negative, T-cell, anaplastic, non-Hodgkin lymphomas (T-ALCL) have been reported worldwide. METHODS: A tumor biopsy specimen from a patient in this series was obtained for characterization. By using a human stromal feeder layer and IL-2, a novel cell line, TLBR-1, was established from this biopsy and investigated by using cytogenetics and various biomolecular methods. RESULTS: Immunoperoxidase staining of the tumor biopsy showed a CD30/CD8/CD4 coexpressing T-cell population that was epithelial membrane antigen (EMA)(+) and perforin(+) . Multiplex polymerase chain reaction (PCR) of TCRgamma genes showed monoclonality that suggested a T-cell origin, yet pan-T markers CD2/5/7, anaplastic large-cell kinase (ALK)-1, pancytokeratins, CD20, CD56, and Epstein-Barr virus (EBV) by in situ hybridization (ISH) were negative. TLBR-1 is IL-2 dependent, has a relatively long doubling time (55 hours), and displays different cellular shapes in culture. Cytogenetic analysis of tumor and TLBR-1 cells confirmed a highly anaplastic cell population with a modal number of 47 chromosomes lacking t(2;5). PCR screens for EBV and human T-lymphotropic virus types 1 and 2 (HTLV-1/2) were negative. Fluorescence-activated cell-sorting (FACS) analysis showed strong positivity for CD4/8, CD30, CD71, and CD26 expression, and antigen presentation (HLA-DR(+) CD80(+) CD86(+) ), IL-2 signaling (CD25(+) CD122(+) ), and NK (CD56(+) ) markers, and Western blots demonstrated strong Notch1 expression. Severe combined immunodeficiency (SCID) mouse TLBR-1 heterotransplants recapitulated the histology and marker characteristics of the original tumor. CONCLUSIONS: TLBR-1, a novel ALK-negative, T-cell, anaplastic, large-cell lymphoma, closely resembles the original biopsy and represents an important tool for studying this newly recognized disease entity.
机译:背景:乳腺原发性淋巴瘤非常罕见(占乳腺恶性肿瘤的0.2-1.5%),绝大多数(95%)是B细胞起源的。最近,全世界已报道40例临床惰性的间变性大细胞激酶(ALK)阴性,T细胞,间变性,非霍奇金淋巴瘤(T-ALCL)。方法:从该系列患者的肿瘤活检标本中获取特征。通过使用人类基质饲养层和IL-2,从该活检中建立了新型细胞系TLBR-1,并通过细胞遗传学和各种生物分子方法进行了研究。结果:肿瘤活检的免疫过氧化物酶染色显示CD30 / CD8 / CD4共表达的T细胞群是上皮膜抗原(EMA)(+)和穿孔素(+)。 TCRgamma基因的多重聚合酶链反应(PCR)显示单克隆性,表明存在T细胞起源,但泛T标记CD2 / 5/7,间变性大细胞激酶(ALK)-1,泛细胞角蛋白,CD20,CD56和爱泼斯坦-Barr病毒(EBV)通过原位杂交(ISH)阴性。 TLBR-1是IL-2依赖性的,具有相对较长的加倍时间(55小时),并且在培养中显示出不同的细胞形状。肿瘤和TLBR-1细胞的细胞遗传学分析确认了高度变性细胞群,其中模态数为47个缺少t(2; 5)的染色体。 EBV和1型和2型人类T淋巴病毒(HTLV-1 / 2)的PCR筛选均为阴性。荧光激活细胞分选(FACS)分析显示对CD4 / 8,CD30,CD71和CD26表达以及抗原呈递(HLA-DR(+)CD80(+)CD86(+)),IL-2信号转导具有强阳性(CD25(+)CD122(+))和NK(CD56(+))标记,Western印迹显示强大的Notch1表达。严重的联合免疫缺陷(SCID)小鼠TLBR-1异种移植概括了原始肿瘤的组织学和标志物特征。结论:TLBR-1是一种新型的ALK阴性,T细胞,间变性,大细胞淋巴瘤,与原始的活检组织非常相似,是研究这一新发现的疾病实体的重要工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号