首页> 外文期刊>Human Pathology >V-ets erythroblastosis virus E26 oncogene homolog (avian)/Trefoil factor 3/high-molecular-weight cytokeratin triple immunostain: A novel tissue-based biomarker in prostate cancer with potential clinical application
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V-ets erythroblastosis virus E26 oncogene homolog (avian)/Trefoil factor 3/high-molecular-weight cytokeratin triple immunostain: A novel tissue-based biomarker in prostate cancer with potential clinical application

机译:V型红细胞滋养细胞病毒E26癌基因同源物(禽)/三叶因子3 /高分子量细胞角蛋白三重免疫染色:一种新型的基于组织的前列腺癌生物标志物,具有潜在的临床应用

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摘要

Summary Trefoil factor 3 (TFF3) is associated with various cancers and overexpressed in a subset of prostate cancers. Functional studies suggest that v-ets erythroblastosis virus E26 oncogene homolog (avian) (ERG) down-regulates TFF3 expression in hormone-na?ve prostate cancer. To characterize this inverse relationship, we developed a triple immunostain encompassing ERG, TFF3, and high-molecular-weight cytokeratin. Triple stain was performed on 96 tumors and 52 benign cases represented in tissue microarrays. Distinct ERG and TFF3 protein was expressed in 45% (43/96) and 36% (35/96) of prostate cancers, respectively. Coexpression was observed in 5% (5/96) of tumor cases, and 24% (23/96) did not express ERG or TFF3. The inverse expression of ERG and TFF3 was significant (P <.0001), with 57% (30/53) of ERG-negative tumors demonstrating TFF3 expression. Sensitivity and specificity of combined ERG and TFF3 expression in detecting prostate cancer were 76% and 96%, respectively. The feasibility of triple immunostain protocol was validated in a set of 76 needle biopsies. The application of this multiplex in situ biomarker for molecular characterization of prostate cancer and as a supplemental diagnostic and prognostic tool in prostate needle biopsies should be further explored.
机译:摘要三叶因子3(TFF3)与多种癌症相关,并在一部分前列腺癌中过表达。功能研究表明,v-ets系红细胞增生病毒E26癌基因同源物(禽)(ERG)下调了初治激素的前列腺癌中TFF3的表达。为了表征这种反比关系,我们开发了包含ERG,TFF3和高分子量细胞角蛋白的三重免疫染色。对组织微阵列中代表的96例肿瘤和52例良性病例进行了三重染色。分别在45%(43/96)和36%(35/96)的前列腺癌中表达了不同的ERG和TFF3蛋白。在5%(5/96)的肿瘤病例中观察到共表达,而24%(23/96)不表达ERG或TFF3。 ERG和TFF3的反向表达很明显(P <.0001),其中ERG阴性的肿瘤中有57%(30/53)证明了TFF3的表达。 ERG和TFF3联合表达在检测前列腺癌中的敏感性和特异性分别为76%和96%。在一组76针活检中验证了三重免疫染色方案的可行性。应当进一步探索这种多重原位生物标志物在前列腺癌分子表征中的应用以及作为前列腺穿刺活检的辅助诊断和预后工具。

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