Department of Genetics, Portuguese Oncology Institute-Porto, Porto, Portugal.
PLoS One. 2012;7(11):e49819. doi: 10.1371/journal.pone.0049819. Epub 2012 Nov 19.
FLI1 and ERG, the major ETS transcription factors involved in rearrangements in the Ewing's sarcoma family of tumors (ESFT) and in prostate carcinomas (PCa), respectively, belong to the same subfamily, having 98% sequence identity in the DNA binding domain. We therefore decided to investigate whether the aberrant transcription factors in both malignancies have some common downstream targets. We crossed a publicly available list of all putative EWSR1-FLI1 target genes in ESFT with our microarray expression data on 24 PCa and 6 non-malignant prostate tissues (NPT) and choose four genes among the top-most differentially expressed between PCa with (PCa ERG+) and without (PCa ETS-) ETS fusion genes (HIST1H4L, KCNN2, ECRG4 and LDOC1), as well as four well-validated direct targets of the EWSR1-FLI1 chimeric protein in ESFT (NR0B1, CAV1, IGFBP3 and TGFBR2). Using quantitative expression analysis in 16 ESFT and seven alveolar rhabdomyosarcomas (ARMS), we were able to validate the four genes previously described as direct targets of the EWSR1-FLI1 oncoprotein, showing overexpression of CAV1 and NR0B1 and underexpression of IGFBP3 and TGFBR2 in ESFT as compared to ARMS. Although none of these four genes showed significant expression differences between PCa ERG+ and PCa ETS-, CAV1, IGFBP3 and TGFBR2 were less expressed in PCa in an independent series of 56 PCa and 15 NPT, as also observed for ECRG4 and LDOC1, suggesting a role in prostate carcinogenesis in general. On the other hand, we demonstrate for the first time that both HIST1H4L and KCNN2 are significantly overexpressed in PCa ERG+ and that ERG binds to the promoter of these genes. Conversely, KCNN2 was found underexpressed in ESFT relative to ARMS, suggesting that the EWSR1-ETS oncoprotein may have the opposite effect of ERG rearrangements in PCa. We conclude that aberrant ETS transcription factors modulate target genes differently in ESFT and PCa.
FLI1 和 ERG 分别是 Ewing 肉瘤家族肿瘤(ESFT)和前列腺癌(PCa)中涉及重排的主要 ETS 转录因子,它们属于同一亚家族,在 DNA 结合域具有 98%的序列同一性。因此,我们决定研究这两种恶性肿瘤中的异常转录因子是否具有一些共同的下游靶标。我们将 ESFT 中所有推定的 EWSR1-FLI1 靶基因的公开列表与我们在 24 例 PCa 和 6 例非恶性前列腺组织(NPT)上的微阵列表达数据进行了交叉,然后选择了在 PCa 中差异表达最显著的四个基因(PCa ERG+)和没有 ETS 融合基因的 PCa(PCa ETS-)(HIST1H4L、KCNN2、ECRG4 和 LDOC1),以及 ESFT 中 EWSR1-FLI1 嵌合蛋白的四个经过充分验证的直接靶标(NR0B1、CAV1、IGFBP3 和 TGFBR2)。在 16 例 ESFT 和 7 例肺泡横纹肌肉瘤(ARMS)中进行定量表达分析后,我们能够验证之前被描述为 EWSR1-FLI1 癌蛋白直接靶标的四个基因,结果显示 CA V1 和 NR0B1 在 ESFT 中过表达,而 IGFBP3 和 TGFBR2 在 ESFT 中表达下调与 ARMS 相比。尽管这四个基因在 PCa ERG+和 PCa ETS-之间没有显示出显著的表达差异,但在另一项 56 例 PCa 和 15 例 NPT 的独立系列中,CA V1、IGFBP3 和 TGFBR2 的表达水平较低,这也与 ECRG4 和 LDOC1 的表达水平较低相似,表明它们在前列腺癌的发生中具有一般作用。另一方面,我们首次证明 HIST1H4L 和 KCNN2 在 PCa ERG+中显著过表达,并且 ERG 结合到这些基因的启动子上。相反,在 ESFT 中,KCNN2 的表达水平低于 ARMS,这表明 EWSR1-ETS 癌蛋白可能在 PCa 中具有与 ERG 重排相反的作用。我们的结论是,异常的 ETS 转录因子在 ESFT 和 PCa 中对靶基因的调节作用不同。