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Gene fusions find an ERG-way to tumor inflammation.

机译:基因融合发现了肿瘤炎症的ERG途径。

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摘要

Gene fusions between the prostate-specific and androgen responsive TMPRSS2 gene and ETS transcription factors occur with distinct frequencies in the early stages of human prostate cancer. These transcription factors are members of the eryth-roblast transformation specific (ETS) family of genes, which are essential to the regulation of cell growth and differentiation. Expression of transcription factors encoded by ETS related gene 1 (ERG1) is elevated in prostate cancer cells and a functional contribution of ERG to the malignant transformation of prostate epithelial cells has been established.3 Under the power of its own promoter ERG1 presents a minimal threat, but a molecular subtype identified in prostate cancer cells is characterized by a fusion of the 5' untranslated region of TMPRSS2 to ERG, previously identified as an androgen regulated promoter. ERG1 and TRMPSS2 are about 3 Mb apart on human chromosome 21q22.2 and such gene fusions have been identified in approximately 50% of prostate cancers.
机译:前列腺特异性雄激素响应性TMPRSS2基因与ETS转录因子之间的基因融合在人类前列腺癌的早期以不同的频率发生。这些转录因子是红细胞转化特异性(ETS)基因家族的成员,对调节细胞的生长和分化至关重要。由ETS相关基因1(ERG1)编码的转录因子的表达在前列腺癌细胞中升高,并且已确定ERG对前列腺上皮细胞恶性转化的功能性贡献。3在其自身启动子的作用下,ERG1的威胁很小,但在前列腺癌细胞中鉴定出的分子亚型的特征是TMPRSS2的5'非翻译区与ERG(先前已确定为雄激素调节的启动子)融合。 ERG1和TRMPSS2在人染色体21q22.2上相距约3 Mb,并且这种基因融合已在大约50%的前列腺癌中得到鉴定。

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