Work

Androgen receptor amplification is concordant between circulating tumor cells and biopsies from men undergoing treatment for metastatic castration resistant prostate cancer

Year: 2017

Type: article

Abstract: // Jennifer Podolak 1 , Kristi Eilers 1 , Timothy Newby 1 , Rachel Slottke 1 , Erin Tucker 1 , Susan B. Olson 2 , Hui-Wen Lue 1 , Jack Youngren 3 , Rahul Aggarwal 3 , Eric J. Small 3 , Julie N. Graff 1 , Joshi J. Alumkal 1 , Tomasz M. Beer 1 and George V. Thomas 1, 2 1 Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA 2 Department of Pathology and Laboratory Medicine, Oregon Health and Science University, Portland, OR, USA 3 School of Medicine, University of California, San Francisco, CA, USA Correspondence to: George V. Thomas, email: [email protected] Keywords: prostate cancer, circulating tumor cells, androgen receptor, metastases, metastatic castration resistant prostate cancer Received: September 30, 2016 Accepted: February 27, 2017 Published: March 13, 2017 ABSTRACT Increased AR activity has been shown to be preserved in spatially distinct metastatic tumors from the same patient suggesting the requirement for lineage-specific dependencies for metastatic castration resistant prostate cancer (mCRPC). Amplification of the AR gene is a common mechanism by which mCRPC increase AR activity. To determine whether AR amplification in circulating tumor cells (CTC) could complement metastatic tissue biopsies in men undergoing treatment for mCRPC, we developed a novel two-step assay to isolate CTCs and subsequently analyzed AR amplification status in CTCs and matched biopsy tissue from the same patient by fluorescence in situ hybridization (FISH). AR gene status in CTCs showed strong concordance with AR gene status in matched tissue samples in 24 of 25 patients (Correlation: 96%; Kappa: 0.83; Sensitivity: 100%, Specificity: 83%). Our work demonstrates that AR amplification is conserved between CTCs and biopsies and that CTCs can serve as non-invasive surrogate to document AR amplification in mCRPC.

Source: Oncotarget

DOI: 10.18632/oncotarget.16169