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通过基因组和功能分析鉴定 NK 细胞肿瘤中的 FOXO3 和 PRDM1 作为肿瘤抑制基因候选物。

Identification of FOXO3 and PRDM1 as tumor-suppressor gene candidates in NK-cell neoplasms by genomic and functional analyses.

机构信息

Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya, Japan.

出版信息

Blood. 2011 Sep 22;118(12):3195-204. doi: 10.1182/blood-2011-04-346890. Epub 2011 Jun 20.

Abstract

Oligo-array comparative genomic hybridization (CGH) and gene-expression profiling of natural killer (NK)-cell neoplasms were used in an effort to delineate the molecular pathogenesis involved. Oligo-array CGH identified two 6q21 regions that were most frequently deleted (14 of 39 or 36%). One of these regions included POPDC3, PREP, PRDM1, ATG5, and AIM1, whereas the other included LACE1 and FOXO3. All genes located in these regions, except for POPDC3 and AIM1, were down-regulated in neoplastic samples, as determined by gene-expression analysis, and were therefore considered to be candidate tumor-suppressor genes. A20 and HACE1, the well-known tumor-suppressor genes located on 6q21-23, were included as candidate genes because they also demonstrated frequent genomic deletions and down-regulated expression. The Tet-Off NK cell line NKL was subsequently established for functional analyses. Seven candidate genes were transduced into Tet-Off NKL and forced re-expression was induced. Re-expression of FOXO3 and PRDM1 suppressed NKL proliferation, but this was not the case after re-expression of the other genes. This effect was confirmed using another NK cell line, SNK10. Furthermore, genomic analyses detected nonsense mutations of PRDM1 that led to functional inactivation in one cell line and one clinical sample. PRDM1 and FOXO3 are considered to play an important role in the pathogenesis of NK-cell neoplasms.

摘要

寡核苷酸阵列比较基因组杂交 (CGH) 和自然杀伤 (NK) 细胞肿瘤的基因表达谱分析用于阐明涉及的分子发病机制。寡核苷酸阵列 CGH 确定了两个最常缺失的 6q21 区域(39 个或 36%中的 14 个)。这些区域之一包括 POPDC3、PREP、PRDM1、ATG5 和 AIM1,而另一个区域包括 LACE1 和 FOXO3。通过基因表达分析确定,这些区域中除了 POPDC3 和 AIM1 之外的所有基因在肿瘤样本中均下调,因此被认为是候选肿瘤抑制基因。A20 和 HACE1 是位于 6q21-23 上的众所周知的肿瘤抑制基因,被选为候选基因,因为它们也表现出频繁的基因组缺失和下调表达。随后建立了 Tet-Off NK 细胞系 NKL 进行功能分析。将七个候选基因转导到 Tet-Off NKL 中,并诱导强制重新表达。FOXO3 和 PRDM1 的重新表达抑制了 NKL 的增殖,但其他基因的重新表达则不然。这一效应在另一个 NK 细胞系 SNK10 中得到了证实。此外,基因组分析在一个细胞系和一个临床样本中检测到 PRDM1 的无意义突变,导致其功能失活。PRDM1 和 FOXO3 被认为在 NK 细胞肿瘤的发病机制中发挥重要作用。

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