前列腺癌
雄激素受体
抗体
循环肿瘤细胞
克隆(Java方法)
癌症研究
癌症
生物标志物
免疫组织化学
计算生物学
生物
医学
内科学
免疫学
基因
转移
生物化学
作者
Tanzila Khan,John G. Lock,Yafeng Ma,David G. Harman,Paul de Souza,Wei Chua,Bavanthi Balakrishnar,Kieran F. Scott,Therese M. Becker
标识
DOI:10.1038/s41598-022-20079-w
摘要
Abstract Androgen receptor variant 7 (AR-V7) is an important biomarker to guide treatment options for castration-resistant prostate cancer (CRPC) patients. Its detectability in circulating tumour cells (CTCs) opens non-invasive diagnostic avenues. While detectable at the transcript level, AR-V7 protein detection in CTCs may add additional information and clinical relevance. The aim of this study was to compare commercially available anti-AR-V7 antibodies and establish reliable AR-V7 immunocytostaining applicable to CTCs from prostate cancer (PCa) patients. We compared seven AR-V7 antibodies by western blotting and immmunocytostaining using a set of PCa cell lines with known AR/AR-V7 status. The emerging best antibody was validated for detection of CRPC patient CTCs enriched by negative depletion of leucocytes. The anti-AR-V7 antibody, clone E308L emerged as the best antibody in regard to signal to noise ratio with a specific nuclear signal. Moreover, this antibody detects CRPC CTCs more efficiently compared to an antibody previously shown to detect AR-V7 CTCs. We have determined the best antibody for AR-V7 detection of CTCs, which will open future studies to correlate AR-V7 subcellular localization and potential co-localization with other proteins and cellular structures to patient outcomes.
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