Evidence map›Paper›PMID 42426451›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Androgen Receptor Variant 7 (AR-V7) Protein Detection in Circulating Tumor Cells by Immunocytostaining.

Tanzila Khan, Yafeng Ma, John Lock, Paul de Souza, David Harman, Wei Chua, Bavanthi Balakrishnar, Kieran Scott, Therese M Becker

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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Tanzila KhanIngham Institute Applied and Medical Research, Liverpool, NSW, Australia. tanzila.khan@inghaminstitute.org.au.
Yafeng MaIngham Institute Applied and Medical Research, Liverpool, NSW, Australia.
John LockSchool of Clinical Medicine, University of New South Wales, Sydney, NSW, Australia.
Paul de SouzaSchool of Clinical Medicine, University of New South Wales, Sydney, NSW, Australia.
David HarmanSchool of Medicine, Western Sydney University, Sydney, NSW, Australia.
Wei ChuaLiverpool Hospital, Liverpool, NSW, Australia.
Bavanthi BalakrishnarLiverpool Hospital, Liverpool, NSW, Australia.
Kieran ScottSchool of Medicine, Western Sydney University, Sydney, NSW, Australia.
Therese M BeckerIngham Institute Applied and Medical Research, Liverpool, NSW, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precision medicine prostate cancer drug development, which targets patient-specific molecular alterations in prostate cancer cells, is rapidly progressing. Traditionally, tissue samples are used to screen for and study molecular alterations, but liquid biopsies are emerging as practical and potentially superior methodologies to longitudinally characterize cancer cell biology and evolution. The expression of androgen receptor variants correlates with the development of castrate resistance prostate cancer (CRPC), and the most studied variant 7 (AR-V7) is associated with CRPC, disease progression, and resistance to certain AR-pathway targeted treatments and is readily detectable in circulating tumor cells (CTCs). While mainly detected at the transcript level, subcellular localization of the protein defines its activity as a transcription factor, and emerging evidence suggests that detection of nuclear AR-V7 in CTCs is central to its utility as a poor-prognosis biomarker. Thus, transcript and protein detection of the AR-V7 biomarker in CTCs may complement each other to achieve the highest sensitivity and specificity. Here, we describe a method of AR-V7 protein detection in CTCs using immunocytostaining.

Indexed as

Biomarkers, TumorImmunohistochemistryNeoplastic Cells, CirculatingProstatic NeoplasmsProstatic Neoplasms, Castration-ResistantReceptors, AndrogenCell Line, TumorHumansMaleAR protein, humanBiomarkers, TumorReceptors, AndrogenAndrogen receptor (AR)Androgen receptor variant 7 (AR-V7)Circulating tumor cell (CTC)ImmunocytostainingProstate cancer

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.