PO.CL01.06 · 临床研究

用于癌症研究的可靠抗体:TROP2作为Abcam增强验证框架的案例研究

Reliable antibodies for cancer research: TROP2 as a case study of Abcam's enhanced validation framework

海报缩略图:用于癌症研究的可靠抗体:TROP2作为Abcam增强验证框架的案例研究
编号 7733 展板 24 时间 4/22 09:00–12:00 区域 Section 41 主讲 Caroline Anderson (Hirst)
分会场 Biomarkers Predictive of Therapeutic Benefit 6
查看 PDF 下载 PDF 🔒 查看 / 下载完整 PDF 需登录并开通下载套餐 · 查看套餐 / 开通 AACR 官方页面

作者与单位 Authors & Affiliations

Caroline S. Hirst, JK Tanjore Ramanathan, Nadine Nelson, Antonella Galli, Will Howat, Silvia Sbacchi

Abcam Limited, Cambridge, United Kingdom

摘要 Abstract

中文摘要
可靠的抗体性能对癌症研究至关重要,尤其是在研究TROP2等疾病相关靶点时。传统的抗体验证方法在应对人体组织表达的复杂性和疾病异质性方面往往不足。为克服这些局限,开发了一种整合疾病相关组织分析的增强验证框架。该方法结合了多个验证步骤,包括敲除验证测试,以及使用自动化免疫组化(IHC)平台在选定的福尔马林固定石蜡包埋(FFPE)人体组织微阵列(TMA)中生成详细的IHC表达谱。作为案例研究,一种靶向TROP2的重组兔单克隆抗体(RabMab®)克隆EPR20043(ab214488)在多个IHC自动化平台上进行了验证。该抗体表现出高特异性,在由TACSTD2敲除MCF7细胞(ab286330)制备的FFPE细胞团中通过IHC未检测到TROP2。此外,对多癌种TMA(乳腺癌、肺癌、卵巢癌和子宫内膜癌)的AI驱动表达谱分析揭示了检测多样蛋白表达水平的高灵敏度,支持其在不同疾病环境中用于生物标志物评估、患者分层和诊断应用的潜力。本研究凸显了增强抗体验证在降低试剂选择风险及确保癌症研究中稳健、可重复结果方面的价值。TROP2案例例证了Abcam严格的抗体验证如何加速肿瘤学研究中的发现和转化应用。
查看英文原文 English abstract
Reliable antibody performance is essential for cancer research, particularly when investigating disease-associated targets such as TROP2. Conventional antibody validation methods often fall short in addressing the complexity of human tissue expression and disease heterogeneity. To overcome these limitations, an enhanced validation framework was developed that integrates disease-relevant tissue profiling. This approach combines multiple validation steps, including knock out validation testing and generating detailed IHC expression profiles in selected formalin-fixed paraffin-embedded (FFPE) human tissue microarrays (TMA) using automated immunohistochemistry (IHC) platforms. As a case study, a recombinant rabbit monoclonal antibody (RabMab®) targeting TROP2, clone EPR20043 (ab214488) was validated across multiple IHC automated platforms. The antibody demonstrated high specificity, with no TROP2 detected by IHC in FFPE cell pellets prepared from TACSTD2 knockout MCF7 cells (ab286330). Furthermore, AI-driven expression profiling of multi-cancer TMAs (breast, lung, ovarian and endometrial cancer) revealed high sensitivity for detecting diverse protein expression levels, supporting its potential for biomarker assessment, patient stratification and diagnostic applications across varied disease settings. This study highlights the value of enhanced antibody validation in de-risking reagent selection and ensuring robust, reproducible results in cancer research. The TROP2 case exemplifies how rigorous Abcam's antibody validation can accelerate discovery and translational applications in the oncology research.
利益披露 Disclosure
C. S. Hirst, Abcam Limited Employment. J. Ramanathan, Abcam Limited Employment. N. Nelson, Abcam Limited Employment. A. Galli, Abcam Limited Employment. W. Howat, Abcam Limited Employment. S. Sbacchi, Abcam Limited Employment.

← 返回 AACR 2026 检索