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前列腺癌去势抵抗的生物标志物:通过多重液滴数字PCR检测雄激素受体扩增和T877A突变

Biomarkers of Castrate Resistance in Prostate Cancer: Androgen Receptor Amplification and T877A Mutation Detection by Multiplex Droplet Digital PCR.

作者信息

Young Francis P, Becker Therese M, Nimir Mohammed, Opperman Thomas, Chua Wei, Balakrishnar Bavanthi, de Souza Paul, Ma Yafeng

机构信息

Centre for Circulating Tumour Cell Diagnostics and Research, Ingham Institute for Applied Medical Research, Liverpool, NSW 2170, Australia.

South Western Clinical School, University of New South Wales, Liverpool, NSW 2170, Australia.

出版信息

J Clin Med. 2022 Jan 4;11(1):257. doi: 10.3390/jcm11010257.

Abstract

Androgen Receptor (AR) alterations (amplification, point mutations, and splice variants) are master players in metastatic castration resistant prostate cancer (CRPC) progression and central therapeutic targets for patient management. Here, we have developed two multiplexed droplet digital PCR (ddPCR) assays to detect AR copy number (CN) and the key point mutation T877A. Overcoming challenges of determining gene amplification from liquid biopsies, these assays cross-validate each other to produce reliable AR amplification and mutation data from plasma cell free DNA (cfDNA) of advanced prostate cancer (PC) patients. Analyzing a mixed PC patient cohort consisting of CRPC and hormone sensitive prostate cancer (HSPC) patients showed that 19% (9/47) patients had AR CN amplification. As expected, only CRPC patients were positive for AR amplification, while interestingly the T877A mutation was identified in two patients still considered HSPC at the time. The ddPCR based analysis of AR alterations in cfDNA is highly economic, feasible, and informative to provide biomarker detection that may help to decide on the best follow-up therapy for CRPC patients.

摘要

雄激素受体(AR)改变(扩增、点突变和剪接变体)是转移性去势抵抗性前列腺癌(CRPC)进展的主要因素,也是患者管理的核心治疗靶点。在此,我们开发了两种多重液滴数字PCR(ddPCR)检测方法,用于检测AR拷贝数(CN)和关键的点突变T877A。这些检测方法克服了从液体活检中确定基因扩增的挑战,相互交叉验证,以从晚期前列腺癌(PC)患者的血浆游离DNA(cfDNA)中产生可靠的AR扩增和突变数据。对由CRPC和激素敏感性前列腺癌(HSPC)患者组成的混合PC患者队列进行分析,结果显示19%(9/47)的患者存在AR CN扩增。正如预期的那样,只有CRPC患者的AR扩增呈阳性,而有趣的是,在当时仍被认为是HSPC的两名患者中发现了T877A突变。基于ddPCR对cfDNA中AR改变的分析具有高度的经济性、可行性和信息性,能够提供生物标志物检测,有助于为CRPC患者确定最佳的后续治疗方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e96/8745706/482b570e60c7/jcm-11-00257-g001.jpg

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