Maeda Takahiro, Hobbs Robin M, Merghoub Taha, Guernah Ilhem, Zelent Arthur, Cordon-Cardo Carlos, Teruya-Feldstein Julie, Pandolfi Pier Paolo
Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, Sloan-Kettering Institute, 1275 York Avenue, New York, New York 10021, USA.
Nature. 2005 Jan 20;433(7023):278-85. doi: 10.1038/nature03203.
Aberrant transcriptional repression through chromatin remodelling and histone deacetylation has been postulated to represent a driving force underlying tumorigenesis because histone deacetylase inhibitors have been found to be effective in cancer treatment. However, the molecular mechanisms by which transcriptional derepression would be linked to tumour suppression are poorly understood. Here we identify the transcriptional repressor Pokemon (encoded by the Zbtb7 gene) as a critical factor in oncogenesis. Mouse embryonic fibroblasts lacking Zbtb7 are completely refractory to oncogene-mediated cellular transformation. Conversely, Pokemon overexpression leads to overt oncogenic transformation both in vitro and in vivo in transgenic mice. Pokemon can specifically repress the transcription of the tumour suppressor gene ARF through direct binding. We find that Pokemon is aberrantly overexpressed in human cancers and that its expression levels predict biological behaviour and clinical outcome. Pokemon's critical role in cellular transformation makes it an attractive target for therapeutic intervention.
通过染色质重塑和组蛋白去乙酰化导致的异常转录抑制被认为是肿瘤发生的驱动力,因为已发现组蛋白去乙酰化酶抑制剂在癌症治疗中有效。然而,转录去抑制与肿瘤抑制相关的分子机制仍知之甚少。在这里,我们确定转录抑制因子Pokemon(由Zbtb7基因编码)是肿瘤发生的关键因素。缺乏Zbtb7的小鼠胚胎成纤维细胞对癌基因介导的细胞转化完全具有抗性。相反,Pokemon的过表达在转基因小鼠的体内外均导致明显的致癌转化。Pokemon可通过直接结合特异性抑制肿瘤抑制基因ARF的转录。我们发现Pokemon在人类癌症中异常过表达,其表达水平可预测生物学行为和临床结果。Pokemon在细胞转化中的关键作用使其成为治疗干预的有吸引力的靶点。