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同源盒基因 NKX2-1 在弥漫性大 B 细胞淋巴瘤中的异位表达是由染色质异常修饰介导的。

Ectopic expression of homeobox gene NKX2-1 in diffuse large B-cell lymphoma is mediated by aberrant chromatin modifications.

机构信息

Department of Human and Animal Cell Lines, Leibniz-Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.

出版信息

PLoS One. 2013 Apr 29;8(4):e61447. doi: 10.1371/journal.pone.0061447. Print 2013.

Abstract

Homeobox genes encode transcription factors ubiquitously involved in basic developmental processes, deregulation of which promotes cell transformation in multiple cancers including hematopoietic malignancies. In particular, NKL-family homeobox genes TLX1, TLX3 and NKX2-5 are ectopically activated by chromosomal rearrangements in T-cell neoplasias. Here, using transcriptional microarray profiling and RQ-PCR we identified ectopic expression of NKL-family member NKX2-1, in a diffuse large B-cell lymphoma (DLBCL) cell line SU-DHL-5. Moreover, in silico analysis demonstrated NKX2-1 overexpression in 5% of examined DLBCL patient samples. NKX2-1 is physiologically expressed in lung and thyroid tissues where it regulates differentiation. Chromosomal and genomic analyses excluded rearrangements at the NKX2-1 locus in SU-DHL-5, implying alternative activation. Comparative expression profiling implicated several candidate genes in NKX2-1 regulation, variously encoding transcription factors, chromatin modifiers and signaling components. Accordingly, siRNA-mediated knockdown and overexpression studies confirmed involvement of transcription factor HEY1, histone methyltransferase MLL and ubiquitinated histone H2B in NKX2-1 deregulation. Chromosomal aberrations targeting MLL at 11q23 and the histone gene cluster HIST1 at 6p22 which we observed in SU-DHL-5 may, therefore, represent fundamental mutations mediating an aberrant chromatin structure at NKX2-1. Taken together, we identified ectopic expression of NKX2-1 in DLBCL cells, representing the central player in an oncogenic regulative network compromising B-cell differentiation. Thus, our data extend the paradigm of NKL homeobox gene deregulation in lymphoid malignancies.

摘要

Homeobox 基因编码转录因子,广泛参与基本的发育过程,其失调会促进包括血液恶性肿瘤在内的多种癌症中的细胞转化。特别是,TLX1、TLX3 和 NKX2-5 等 NKL 家族同源盒基因通过 T 细胞肿瘤中的染色体重排而异常激活。在这里,我们使用转录微阵列分析和 RQ-PCR 鉴定了弥漫性大 B 细胞淋巴瘤 (DLBCL) 细胞系 SU-DHL-5 中 NKL 家族成员 NKX2-1 的异位表达。此外,通过计算分析在 5%的被检查的 DLBCL 患者样本中发现 NKX2-1 过表达。NKX2-1 在肺和甲状腺组织中生理性表达,在这些组织中它调节分化。染色体和基因组分析排除了 SU-DHL-5 中 NKX2-1 基因座的重排,暗示了替代激活。比较表达谱分析表明,在 NKX2-1 调节中涉及几个候选基因,它们分别编码转录因子、染色质修饰剂和信号成分。因此,siRNA 介导的敲低和过表达研究证实了转录因子 HEY1、组蛋白甲基转移酶 MLL 和泛素化组蛋白 H2B 在 NKX2-1 失调中的作用。我们在 SU-DHL-5 中观察到的针对 11q23 上的 MLL 和 6p22 上的组蛋白基因簇 HIST1 的染色体畸变,因此可能代表介导 NKX2-1 异常染色质结构的基本突变。综上所述,我们在 DLBCL 细胞中鉴定出 NKX2-1 的异位表达,它是破坏 B 细胞分化的致癌调节网络中的核心调控因子。因此,我们的数据扩展了 NKL 同源盒基因在淋巴恶性肿瘤中失调的范例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7ef/3639244/634fc9307214/pone.0061447.g001.jpg

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