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PTEN genomic deletion is an early event associated with ERG gene rearrangements in prostate cancer.

机译:PTEN基因组缺失是前列腺癌中与ERG基因重排有关的早期事件。

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OBJECTIVE: To investigate the interaction between, and significance of, ERG gene rearrangements and PTEN genomic deletions in relation to the development and progression of prostate cancer (PCA). PATIENTS AND METHODS: We interrogated an initial cohort of 220 men with localized PCA using fluorescence in situ hybridization for ERG rearrangements and PTEN genomic deletions. RESULTS: The incidences of ERG rearrangements and PTEN deletions in PCA were significantly higher than in high-grade prostatic intra-epithelial neoplasia (HGPIN) and benign prostate tissue (P < 0.001). ERG rearrangements and PTEN deletions were detected in 41.9 and 42.6% of patients' tumours, respectively. ERG rearrangements were never detected in benign prostate tissue, while PTEN aberrations were present at a basal level of 4.6%. PTEN hemizygous deletions showed higher frequency than homozygous deletions within each diagnostic category from benign prostate tissue to HGPIN and PCA (P
机译:目的:探讨ERG基因重排和PTEN基因组缺失与前列腺癌(PCA)的发展之间的相互作用及其意义。病人和方法:我们使用荧光原位杂交技术对ERG重排和PTEN基因组缺失进行了研究,初步调查了220名局部PCA患者。结果:PCA中ERG重排和PTEN缺失的发生率显着高于高级别前列腺上皮内瘤变(HGPIN)和前列腺良性组织(P <0.001)。分别在41.9%和42.6%的患者肿瘤中检测到ERG重排和PTEN缺失。在良性前列腺组织中从未检测到ERG重排,而PTEN畸变的基础水平为4.6%。在从良性前列腺组织到HGPIN和PCA的每个诊断类别中,PTEN半合子缺失显示出比纯合子缺失更高的频率(P

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