• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Ets 相关基因表达水平高对前列腺癌具有高度特异性:对 11483 例癌症的组织微阵列研究。

High level of Ets-related gene expression has high specificity for prostate cancer: a tissue microarray study of 11 483 cancers.

机构信息

Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Histopathology. 2012 Sep;61(3):445-53. doi: 10.1111/j.1365-2559.2012.04240.x. Epub 2012 Mar 28.

DOI:10.1111/j.1365-2559.2012.04240.x
PMID:22463702
Abstract

AIMS

TMPRSS2-ERG fusion resulting in strong Ets-related gene (ERG) overexpression occurs in about 50% of prostate cancers. This study was undertaken to determine the prevalence of ERG overexpression in other tumour types as well as in normal tissues.

METHODS AND RESULTS

A total of 11 483 tumours and 72 different normal tissue types were analysed in a tissue microarray format. Strong nuclear ERG overexpression was found in 36.7% of prostate carcinomas as well as in various vascular tumours, including Kaposi sarcomas (91.7%), angiosarcomas (100%) and haemangiomas (90.9%). Moderate to strong nuclear ERG immunostaining was also observed in thymoma (6.1%). Weak to moderate ERG staining was found in a small number of squamous cell carcinomas of the skin, squamous carcinomas of the lung, malignant mesotheliomas, carcinosarcomas of the uterus, gastrointestinal stromal tumours, hepatocellular carcinomas, teratomas of the testis, anaplastic carcinomas of the thyroid, giant cell tumours of the tendon sheath and benign fibrous histiocytomas of the skin. ERG overexpression was not seen in 8886 samples from 132 other tumour types and subtypes. Within normal tissues, immunohistochemically detectable ERG overexpression was restricted to endothelial cells and subsets of lymphocytes.

CONCLUSIONS

The high specificity of ERG expression in both normal and neoplastic tissues suggests a very narrow biological role for ERG in highly selected tissues.

摘要

目的

TMPRSS2-ERG 融合导致强 Ets 相关基因(ERG)过表达发生在约 50%的前列腺癌中。本研究旨在确定 ERG 过表达在其他肿瘤类型以及正常组织中的发生率。

方法和结果

在组织微阵列格式中分析了总共 11483 个肿瘤和 72 种不同的正常组织类型。在前列腺癌以及各种血管肿瘤中,包括卡波西肉瘤(91.7%)、血管肉瘤(100%)和血管瘤(90.9%)中发现强核 ERG 过表达。在胸腺瘤(6.1%)中也观察到中度至强核 ERG 免疫染色。在少数皮肤鳞状细胞癌、肺鳞状细胞癌、恶性间皮瘤、子宫癌肉瘤、胃肠道间质瘤、肝细胞癌、睾丸生殖细胞瘤、甲状腺间变性癌、腱鞘巨细胞瘤和皮肤良性纤维组织细胞瘤中发现弱至中度 ERG 染色。在来自 132 种其他肿瘤类型和亚型的 8886 个样本中未观察到 ERG 过表达。在正常组织中,免疫组织化学可检测到的 ERG 过表达仅限于内皮细胞和淋巴细胞亚群。

结论

ERG 在正常和肿瘤组织中的高特异性表明 ERG 在高度选择的组织中具有非常狭窄的生物学作用。

相似文献

1
High level of Ets-related gene expression has high specificity for prostate cancer: a tissue microarray study of 11 483 cancers.Ets 相关基因表达水平高对前列腺癌具有高度特异性:对 11483 例癌症的组织微阵列研究。
Histopathology. 2012 Sep;61(3):445-53. doi: 10.1111/j.1365-2559.2012.04240.x. Epub 2012 Mar 28.
2
ERG transcription factor as an immunohistochemical marker for vascular endothelial tumors and prostatic carcinoma.ERG 转录因子作为血管内皮肿瘤和前列腺癌的免疫组化标志物。
Am J Surg Pathol. 2011 Mar;35(3):432-41. doi: 10.1097/PAS.0b013e318206b67b.
3
Frequent TMPRSS2-ERG rearrangement in prostatic small cell carcinoma detected by fluorescence in situ hybridization: the superiority of fluorescence in situ hybridization over ERG immunohistochemistry.荧光原位杂交检测前列腺小细胞癌中 TMPRSS2-ERG 重排的高频发生:荧光原位杂交优于 ERG 免疫组化。
Hum Pathol. 2013 Oct;44(10):2227-33. doi: 10.1016/j.humpath.2013.05.005. Epub 2013 Jul 12.
4
High RNA-binding motif protein 3 expression is an independent prognostic marker in operated prostate cancer and tightly linked to ERG activation and PTEN deletions.高 RNA 结合基序蛋白 3 的表达是手术治疗的前列腺癌的一个独立预后标志物,与 ERG 激活和 PTEN 缺失密切相关。
Eur J Cancer. 2014 Mar;50(4):852-61. doi: 10.1016/j.ejca.2013.12.003. Epub 2013 Dec 28.
5
βIII-tubulin overexpression is an independent predictor of prostate cancer progression tightly linked to ERG fusion status and PTEN deletion.βIII-微管蛋白过表达是前列腺癌进展的一个独立预测因子,与 ERG 融合状态和 PTEN 缺失密切相关。
Am J Pathol. 2014 Mar;184(3):609-17. doi: 10.1016/j.ajpath.2013.11.007. Epub 2013 Dec 28.
6
Marked heterogeneity of ERG expression in large primary prostate cancers.在大型原发性前列腺癌中 ERG 表达存在明显异质性。
Mod Pathol. 2013 Jan;26(1):106-16. doi: 10.1038/modpathol.2012.130. Epub 2012 Aug 17.
7
Saccharomyces cerevisiae-like 1 overexpression is frequent in prostate cancer and has markedly different effects in Ets-related gene fusion-positive and fusion-negative cancers.酿酒酵母样1过表达在前列腺癌中很常见,并且在Ets相关基因融合阳性和融合阴性癌症中具有明显不同的作用。
Hum Pathol. 2015 Apr;46(4):514-23. doi: 10.1016/j.humpath.2014.06.006. Epub 2014 Jun 26.
8
ERG protein expression in human tumors detected with a rabbit monoclonal antibody.用兔单克隆抗体检测人肿瘤中的 ERG 蛋白表达。
Am J Clin Pathol. 2012 Dec;138(6):803-10. doi: 10.1309/AJCP3K5VUFALZTKC.
9
Immunohistochemical evaluation of ERG expression in various benign and malignant tissues.ERG在各种良性和恶性组织中表达的免疫组织化学评估。
Ann Clin Lab Sci. 2013 Winter;43(1):3-9.
10
Morphological features of TMPRSS2-ERG gene fusion prostate cancer.TMPRSS2-ERG基因融合前列腺癌的形态学特征。
J Pathol. 2007 May;212(1):91-101. doi: 10.1002/path.2154.

引用本文的文献

1
Exploring the efficacy of AMACR, ERG, and AR immunostains in prostatic adenocarcinoma and their association with novel grade groups.探索α-甲基酰基辅酶A消旋酶(AMACR)、视网膜电图(ERG)和雄激素受体(AR)免疫染色在前列腺腺癌中的疗效及其与新分级组的关联。
Eur J Histochem. 2025 Feb 11;69(1):4172. doi: 10.4081/ejh.2025.4172.
2
Cadmium, von Willebrand factor and vascular aging.镉、血管性血友病因子与血管衰老
NPJ Aging. 2023 Jun 1;9(1):11. doi: 10.1038/s41514-023-00107-3.
3
Trends in Gene Expression Profiling for Prostate Cancer Risk Assessment: A Systematic Review.
用于前列腺癌风险评估的基因表达谱分析趋势:一项系统综述。
Biomed Hub. 2017 May 17;2(2):1-15. doi: 10.1159/000472146. eCollection 2017 May-Aug.
4
IMP3 overexpression occurs in various important cancer types and is linked to aggressive tumor features: A tissue microarray study on 8,877 human cancers and normal tissues.IMP3 过表达发生在各种重要的癌症类型中,并与侵袭性肿瘤特征相关:在 8877 个人类癌症和正常组织的组织微阵列研究中。
Oncol Rep. 2018 Jan;39(1):3-12. doi: 10.3892/or.2017.6072. Epub 2017 Nov 2.
5
Diagnostic Immunohistochemistry in Cutaneous Neoplasia: An Update.皮肤肿瘤的诊断性免疫组织化学:最新进展
Dermatopathology (Basel). 2015 Apr 8;2(1):15-42. doi: 10.1159/000377698. eCollection 2015 Jan-Mar.
6
TMPRSS2-ERG rearrangement in dominant anterior prostatic tumours: incidence and correlation with ERG immunohistochemistry.TMPRSS2-ERG 重排在前位优势前列腺肿瘤中的发生率及与 ERG 免疫组化的相关性。
Histopathology. 2013 Aug;63(2):279-86. doi: 10.1111/his.12153. Epub 2013 May 23.
7
Usefulness of a monoclonal ERG/FLI1 antibody for immunohistochemical discrimination of Ewing family tumors.用于免疫组织化学鉴别尤文家族肿瘤的单克隆 ERG/FLI1 抗体的实用性。
Am J Clin Pathol. 2013 Jun;139(6):771-9. doi: 10.1309/AJCPN4L1BMRQPEIT.
8
ERG induces epigenetic activation of Tudor domain-containing protein 1 (TDRD1) in ERG rearrangement-positive prostate cancer.ERG 通过诱导包含 Tudor 结构域蛋白 1(TDRD1)的表观遗传激活作用促进 ERG 重排阳性前列腺癌的发生。
PLoS One. 2013;8(3):e59976. doi: 10.1371/journal.pone.0059976. Epub 2013 Mar 29.