2565:利用一种新型高特异性兔单克隆抗体检测人前列腺组织标本中ETV1的表达

Shyh-Han Tan, D. Young, S. Elsamanoudi, J. Kagan, S. Srivastava, A. Dobi, G. Petrovics, I. Sesterhenn, Gregory T. Chesnut
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Our understanding of the role that ETV1 plays in the activation of prostate cancer has been limited by the lack of ETV1 specific antibodies. Methods: A novel ETV1 monoclonal antibody (MAb) was raised by immunization of ETV1 peptides in rabbit followed by screening of hybridomas by ELISA and immunoblot assays. Further screening using exogenously expressed ETV1, ETV4, ETV5, ERG, SPDEF, and FLI1 proteins identified the clone with the most reactive MAb. Purified MAb was used to evaluate ETV1 expression on a tissue micro-array (TMA) constructed from radical prostatectomies of 50 African American (AA) and 50 Caucasian American (CA) patients by immunohistochemistry (IHC). Key residues required for Mab binding were mapped by ELISA using overlapping peptides and alanine scanning. Results: IHC evaluation using the ETV1 specific rabbit Mab on a prostate cancer TMA derived from 100 patients identified five ETV1 positive cases, of whom four were CA. The index tumors for these five ETV1 cases were ERG negative. One patient harbored both ERG positive and ERG negative tumor foci, and as expected, the ETV1 positive tumor focus was ERG negative, and vice versa. Conclusions: We developed a novel rabbit monoclonal ETV1 antibody that is suitable for IHC assay in human prostate tissue. An evaluation of prostate cancer specimens confirmed the reported frequency of ETV1 alteration. Further evaluation using tissue specimens from larger cohorts to establish the sensitivity and specificity of this antibody and validate the utility of ETV1 detection in improving the diagnosis and stratification of prostate and other cancers are in progress. Citation Format: Shyh-Han Tan, Denise Young, Sally Elsamanoudi, Jacob Kagan, Sudhir Srivastava, Albert Dobi, Gyorgy Petrovics, Isabell A. Sesterhenn, Gregory T. Chesnut. Detection of ETV1 expression in human prostate tissue specimens using a novel and highly specific rabbit monoclonal antibody [abstract]. 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引用次数: 0

摘要

引言:ETV1经常参与基因组融合和易位事件,导致其在多种癌症中过表达。这些事件发生在大约5%的前列腺癌中,它们与含有TMPRSS2-ERG融合或PTEN缺失的肿瘤相互排斥。研究表明,高ETV1蛋白表达与前列腺癌预后不良之间存在相关性。据报道,ETV1与KIT协同合作,作为胃肠道间质瘤的一种谱系生存因子。在含有cic重排或CIC-DUX4基因融合的肉瘤亚群中,ETV1的表达为这种癌症的诊断提供了可靠的分子特征。由于缺乏ETV1特异性抗体,我们对ETV1在前列腺癌激活中所起作用的理解受到限制。方法:通过免疫兔ETV1多肽制备一种新的ETV1单克隆抗体(MAb),并采用ELISA和免疫印迹法筛选杂交瘤。进一步筛选外源表达的ETV1、ETV4、ETV5、ERG、SPDEF和FLI1蛋白,鉴定出反应性最强的克隆单克隆抗体。通过免疫组化(IHC)检测50例非裔美国人(AA)和50例高加索美国人(CA)根治性前列腺切除术后构建的组织微阵列(TMA)上ETV1的表达。利用重叠肽和丙氨酸扫描,ELISA绘制了单抗结合所需的关键残基。结果:使用ETV1特异性兔单抗对来自100例患者的前列腺癌TMA进行免疫组化评估,发现5例ETV1阳性病例,其中4例为CA。这5例ETV1病例的指标肿瘤为ERG阴性。1例患者同时存在ERG阳性和ERG阴性的肿瘤病灶,正如预期的那样,ETV1阳性的肿瘤病灶是ERG阴性的,反之亦然。结论:制备了一种适用于人前列腺组织免疫组化检测的兔ETV1单克隆抗体。对前列腺癌标本的评估证实了报道的ETV1改变的频率。目前正在使用更大队列的组织标本进行进一步评估,以确定该抗体的敏感性和特异性,并验证ETV1检测在改善前列腺癌和其他癌症的诊断和分层方面的效用。引文格式:Shyh-Han Tan, Denise Young, Sally Elsamanoudi, Jacob Kagan, Sudhir Srivastava, Albert Dobi, Gyorgy Petrovics, Isabell A. Sesterhenn, Gregory T. Chesnut。一种新型高特异性兔单克隆抗体检测人前列腺组织标本中ETV1的表达[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):2565。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract 2565: Detection of ETV1 expression in human prostate tissue specimens using a novel and highly specific rabbit monoclonal antibody
Introduction: ETV1 is frequently involved in genomic fusions and translocation events that lead to its overexpression in multiple cancers. These events occur in approximately 5% of prostate cancers, which are mutually exclusive from tumors harboring TMPRSS2-ERG fusion or PTEN deletion. Studies suggest a correlation between strong ETV1 protein expression and poor outcome in prostate cancer. ETV1 has been reported to synergistically cooperate with KIT as a lineage survival factor in gastrointestinal stromal tumors. The expression of ETV1 in a subset of sarcomas that harbor CICrearrangements or CIC-DUX4 gene fusions presents a reliable molecular signature for the diagnosis of this cancer. Our understanding of the role that ETV1 plays in the activation of prostate cancer has been limited by the lack of ETV1 specific antibodies. Methods: A novel ETV1 monoclonal antibody (MAb) was raised by immunization of ETV1 peptides in rabbit followed by screening of hybridomas by ELISA and immunoblot assays. Further screening using exogenously expressed ETV1, ETV4, ETV5, ERG, SPDEF, and FLI1 proteins identified the clone with the most reactive MAb. Purified MAb was used to evaluate ETV1 expression on a tissue micro-array (TMA) constructed from radical prostatectomies of 50 African American (AA) and 50 Caucasian American (CA) patients by immunohistochemistry (IHC). Key residues required for Mab binding were mapped by ELISA using overlapping peptides and alanine scanning. Results: IHC evaluation using the ETV1 specific rabbit Mab on a prostate cancer TMA derived from 100 patients identified five ETV1 positive cases, of whom four were CA. The index tumors for these five ETV1 cases were ERG negative. One patient harbored both ERG positive and ERG negative tumor foci, and as expected, the ETV1 positive tumor focus was ERG negative, and vice versa. Conclusions: We developed a novel rabbit monoclonal ETV1 antibody that is suitable for IHC assay in human prostate tissue. An evaluation of prostate cancer specimens confirmed the reported frequency of ETV1 alteration. Further evaluation using tissue specimens from larger cohorts to establish the sensitivity and specificity of this antibody and validate the utility of ETV1 detection in improving the diagnosis and stratification of prostate and other cancers are in progress. Citation Format: Shyh-Han Tan, Denise Young, Sally Elsamanoudi, Jacob Kagan, Sudhir Srivastava, Albert Dobi, Gyorgy Petrovics, Isabell A. Sesterhenn, Gregory T. Chesnut. Detection of ETV1 expression in human prostate tissue specimens using a novel and highly specific rabbit monoclonal antibody [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 2565.
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