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免疫组织化学检测前列腺癌中的 ERG 基因重排状态。

ERG gene rearrangement status in prostate cancer detected by immunohistochemistry.

机构信息

Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.

出版信息

Virchows Arch. 2011 Oct;459(4):441-7. doi: 10.1007/s00428-011-1128-4. Epub 2011 Jul 20.

DOI:10.1007/s00428-011-1128-4
PMID:21773753
Abstract

TMPRSS2-ERG, the most common gene fusion in prostate cancer, is associated with expression of a truncated protein product of the oncogene ERG. A novel anti-ERG monoclonal antibody has been recently characterized. We investigated the correlation between ERG rearrangement assessed by fluorescence in situ hybridization (FISH) and ERG expression detected by immunohistochemistry in a large cohort of patients treated with radical prostatectomy for clinically localized prostate cancer. Thirteen tissue microarrays comprising 305 tumors and a subset of 112 samples of nonneoplastic prostatic tissue were assessed for ERG rearrangement status by FISH and for ERG expression by immunohistochemistry. Accuracy of ERG detection by immunohistochemistry in predicting ERG status as assessed by FISH (criterion standard) was calculated in terms of sensitivity, specificity, positive and negative predictive values. Of 305 tumor foci, 103 (34%) showed ERG rearrangement by FISH. ERG was detected by immunohistochemistry in 100 (33%) cases, 99 of which were FISH positive. ERG detection by immunohistochemistry demonstrated a sensitivity and specificity of 96% and 99%, respectively, with positive and negative predictive values of 99% and 98%, respectively. None of the 112 samples of nonneoplastic prostatic tissue was rearranged by FISH or showed any ERG expression. In conclusion, ERG detection by immunohistochemistry in prostate cancer was highly predictive of ERG rearrangement as assessed by FISH in a large cohort of prostatectomy patients. Given the high yield and the easier task of performing immunohistochemistry vs. FISH, ERG assessment by immunohistochemistry may be useful for characterizing ERG status in prostate cancer.

摘要

TMPRSS2-ERG 是前列腺癌中最常见的基因融合,与致癌基因 ERG 截断蛋白产物的表达相关。最近,一种新型的抗 ERG 单克隆抗体已被描述。我们研究了在接受根治性前列腺切除术治疗的局限性前列腺癌患者的大样本中,荧光原位杂交(FISH)评估的 ERG 重排与免疫组织化学检测的 ERG 表达之间的相关性。使用 FISH 评估了 13 个组织微阵列(包含 305 个肿瘤)和非肿瘤前列腺组织的亚组 112 个样本的 ERG 重排状态,并通过免疫组织化学检测 ERG 表达。通过免疫组织化学检测 ERG 表达预测 FISH(金标准)评估的 ERG 状态的准确性,以灵敏度、特异性、阳性和阴性预测值来计算。在 305 个肿瘤灶中,有 103 个(34%)通过 FISH 显示 ERG 重排。100 个(33%)病例通过免疫组织化学检测到 ERG,其中 99 个为 FISH 阳性。免疫组织化学检测 ERG 的灵敏度和特异性分别为 96%和 99%,阳性和阴性预测值分别为 99%和 98%。112 个非肿瘤前列腺组织样本均未通过 FISH 重排或显示任何 ERG 表达。总之,在接受根治性前列腺切除术的前列腺癌患者的大样本中,免疫组织化学检测 ERG 高度预测了 FISH 评估的 ERG 重排。鉴于免疫组织化学检测的高产量和比 FISH 更容易执行的任务,免疫组织化学检测 ERG 可能有助于描述前列腺癌中的 ERG 状态。

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本文引用的文献

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The positive immunostaining of TMPRSS2-ERG is not associated with unfavourable outcomes and biochemical recurrence after radical prostatectomy in Turkish patients.在土耳其患者中,TMPRSS2-ERG的阳性免疫染色与根治性前列腺切除术后的不良结局和生化复发无关。
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miRNAs as drivers of TMPRSS2-ERG negative prostate tumors in African American men.miRNAs 作为非裔美国男性中 TMPRSS2-ERG 阴性前列腺肿瘤的驱动因素。
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J Cancer. 2010 Oct 25;1:197-208. doi: 10.7150/jca.1.197.
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ERG rearrangement is present in a subset of transition zone prostatic tumors.ERG 重排存在于一部分移行区前列腺肿瘤中。
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ERG oncoprotein expression in prostate cancer: clonal progression of ERG-positive tumor cells and potential for ERG-based stratification.前列腺癌中 ERG 癌基因蛋白的表达:ERG 阳性肿瘤细胞的克隆演进及基于 ERG 的分层潜能。
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ERG rearrangement is specific to prostate cancer and does not occur in any other common tumor.ERG 重排是前列腺癌特有的,不会发生在任何其他常见肿瘤中。
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Prevalence of TMPRSS2-ERG and SLC45A3-ERG gene fusions in a large prostatectomy cohort.在一个大型前列腺切除术队列中 TMPRSS2-ERG 和 SLC45A3-ERG 基因融合的流行率。
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