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弥漫性大B细胞淋巴瘤中2p15 - 16扩增子处靶基因的特征分析。

Characterization of target genes at the 2p15-16 amplicon in diffuse large B-cell lymphoma.

作者信息

Fukuhara Noriko, Tagawa Hiroyuki, Kameoka Yoshihiro, Kasugai Yumiko, Karnan Sivasundaram, Kameoka Junichi, Sasaki Takeshi, Morishima Yasuo, Nakamura Shigeo, Seto Masao

机构信息

Division of Molecular Medicine, Aichi Cancer Center Research Institute, Nagoya 464-8681, Japan.

出版信息

Cancer Sci. 2006 Jun;97(6):499-504. doi: 10.1111/j.1349-7006.2006.00209.x.

Abstract

Amplification of 2p has been observed as a recurrent alteration in diffuse large B-cell lymphoma (DLBCL). Whereas two candidate oncogenes, REL and BCL11A, have been investigated as targets for 2p amplification, the question remains as to whether the true target gene in the amplicon is REL, BCL11A or both. We previously identified frequent genomic gains of chromosomal 2p in 25 out of 99 DLBCL cases by means of genome-wide array comparative genomic hybridization (CGH). All of these 25 cases included recurrent copy number gain at 2p15-16. In the study presented here, cases were analyzed in greater detail by means of contig bacterial artificial chromosome (BAC) array CGH for the 4.5-Mb region at 2p15-16, which contained 33 BAC clones. We confined the minimal common region to 500-kb in length, where only the candidate oncogene REL, and not BCL11A, is located. Real-time quantitative PCR was carried out to investigate the correlation between genomic gain and expression. It showed a significant correlation for both genes, indicating that these two genes are common targets for the 2p15-16 amplicon. However, given the fact that REL is more frequently amplified than BCL11A, the REL gene may play a more important role than BCL11A in the pathogenesis of DLBCL.

摘要

2p扩增已被视作弥漫性大B细胞淋巴瘤(DLBCL)中反复出现的改变。尽管已对两个候选癌基因REL和BCL11A作为2p扩增的靶点进行了研究,但扩增子中的真正靶基因是REL、BCL11A还是两者,这一问题仍然存在。我们之前通过全基因组阵列比较基因组杂交(CGH)在99例DLBCL病例中的25例中鉴定出了染色体2p频繁的基因组增益。所有这25例病例均包括2p15 - 16处反复出现的拷贝数增加。在本研究中,通过重叠群细菌人工染色体(BAC)阵列CGH对2p15 - 16处4.5 Mb区域(包含33个BAC克隆)进行了更详细的病例分析。我们将最小共同区域限定为长度500 kb,其中仅定位了候选癌基因REL,而未定位BCL11A。进行了实时定量PCR以研究基因组增益与表达之间的相关性。结果显示这两个基因均存在显著相关性,表明这两个基因是2p15 - 16扩增子的共同靶点。然而,鉴于REL比BCL11A更频繁地被扩增,REL基因在DLBCL发病机制中可能比BCL11A发挥更重要的作用。

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