Linn Douglas E, Bronson Roderick T, Li Zhe
Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts 02115, United States of America; Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115, United States of America.
Rodent Histopathology, Harvard Medical School, Boston, Massachusetts 02115, United States of America.
PLoS One. 2015 Mar 17;10(3):e0120628. doi: 10.1371/journal.pone.0120628. eCollection 2015.
Gene fusions involving ETS family transcription factors (mainly TMPRSS2-ERG and TMPRSS2-ETV1 fusions) have been found in ~50% of human prostate cancer cases. Although expression of TMPRSS2-ERG or TMPRSS2-ETV1 fusion alone is insufficient to initiate prostate tumorigenesis, they appear to sensitize prostate epithelial cells for cooperation with additional oncogenic mutations to drive frank prostate adenocarcinoma. To search for such ETS-cooperating oncogenic events, we focused on a well-studied prostate tumor suppressor NKX3.1, as loss of NKX3.1 is another common genetic alteration in human prostate cancer. Previous studies have shown that deletions at 8p21 (harboring NKX3.1) and 21q22 (resulting in TMPRSS2-ERG fusion) were both present in a subtype of prostate cancer cases, and that ERG can lead to epigenetic silencing of NKX3.1 in prostate cancer cells, whereas NKX3.1 can in turn negatively regulate TMPRSS2-ERG fusion expression via suppression of the TMPRSS2 promoter activity. We recently generated knockin mouse models for TMPRSS2-ERG and TMPRSS2-ETV1 fusions, utilizing the endogenous Tmprss2 promoter. We crossed these knockin models to an Nkx3.1 knockout mouse model. In Tmprss2-ERG;Nkx3.1+/- (or -/-) male mice, although we observed a slight but significant upregulation of Tmprss2-ERG fusion expression upon Nkx3.1 loss, we did not detect any significant cooperation between these two genetic events to enhance prostate tumorigenesis in vivo. Furthermore, retrospective analysis of a previously published human prostate cancer dataset revealed that within ERG-overexpressing prostate cancer cases, NKX3.1 loss or deletion did not predict biochemical relapse after radical prostatectomy. Collectively, these data suggest that although TMPRSS2-ERG fusion and loss of NKX3.1 are among the most common mutational events found in prostate cancer, and although each of them can sensitize prostate epithelial cells for cooperating with other oncogenic events, these two events themselves do not appear to cooperate at a significant level in vivo to enhance prostate tumorigenesis.
在约50%的人类前列腺癌病例中发现了涉及ETS家族转录因子的基因融合(主要是TMPRSS2-ERG和TMPRSS2-ETV1融合)。虽然单独的TMPRSS2-ERG或TMPRSS2-ETV1融合表达不足以启动前列腺肿瘤发生,但它们似乎使前列腺上皮细胞对与其他致癌突变的合作敏感,从而驱动明显的前列腺腺癌。为了寻找这种与ETS协同作用的致癌事件,我们聚焦于一个经过充分研究的前列腺肿瘤抑制因子NKX3.1,因为NKX3.1的缺失是人类前列腺癌中另一种常见的基因改变。先前的研究表明,8p21(包含NKX3.1)和21q22(导致TMPRSS2-ERG融合)的缺失在一部分前列腺癌病例中均存在,并且ERG可导致前列腺癌细胞中NKX3.1的表观遗传沉默,而NKX3.1反过来可通过抑制TMPRSS2启动子活性来负向调节TMPRSS2-ERG融合表达。我们最近利用内源性Tmprss2启动子构建了TMPRSS2-ERG和TMPRSS2-ETV1融合的基因敲入小鼠模型。我们将这些基因敲入模型与Nkx3.1基因敲除小鼠模型进行杂交。在Tmprss2-ERG;Nkx3.1+/-(或-/-)雄性小鼠中,虽然我们观察到Nkx3.1缺失后Tmprss2-ERG融合表达有轻微但显著的上调,但我们未检测到这两个基因事件在体内增强前列腺肿瘤发生方面有任何显著的协同作用。此外,对先前发表的人类前列腺癌数据集的回顾性分析显示,在ERG过表达的前列腺癌病例中,NKX3.1的缺失或缺失并不能预测根治性前列腺切除术后的生化复发。总体而言,这些数据表明,虽然TMPRSS2-ERG融合和NKX3.1的缺失是前列腺癌中最常见的突变事件之一,并且虽然它们各自都能使前列腺上皮细胞对与其他致癌事件的合作敏感,但这两个事件本身在体内似乎并没有显著的协同作用来增强前列腺肿瘤发生。