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Published on: December 15, 2017
AR-V7 and resistance to enzalutamide and abiraterone in prostate cancer
Emmanuel S Antonarakis1, Changxue Lu, Hao Wang
1From the Departments of Oncology (E.S.A., H.W., B.L., J.T.I., R.N., C.J.P., S.R.D., M.A.C., M.A.E.), Pathology (H.L.F., T.L.L., Q.Z., A.M.D.M.), and Urology (C.L., M.N., J.C.R., Yan Chen, W.B.I., J.L.), Johns Hopkins University School of Medicine, Baltimore; and Greehey Children's Cancer Research Institute (T.A.M., Yidong Chen) and the Department of Epidemiology and Biostatistics (Yidong Chen), University of Texas Health Science Center at San Antonio, San Antonio.
Background:
The androgen-receptor isoform encoded by splice variant 7 lacks the ligand-binding domain, which is the target of enzalutamide and abiraterone, but remains constitutively active as a transcription factor. We hypothesized that detection of androgen-receptor splice variant 7 messenger RNA (AR-V7) in circulating tumor cells from men with advanced prostate cancer would be associated with resistance to enzalutamide and abiraterone.
Methods:
We used a quantitative reverse-transcriptase-polymerase-chain-reaction assay to evaluate AR-V7 in circulating tumor cells from prospectively enrolled patients with metastatic castration-resistant prostate cancer who were initiating treatment with either enzalutamide or abiraterone. We examined associations between AR-V7 status (positive vs. negative) and prostate-specific antigen (PSA) response rates (the primary end point), freedom from PSA progression (PSA progression-free survival), clinical or radiographic progression-free survival, and overall survival.
Results:
A total of 31 enzalutamide-treated patients and 31 abiraterone-treated patients were enrolled, of whom 39% and 19%, respectively, had detectable AR-V7 in circulating tumor cells. Among men receiving enzalutamide, AR-V7-positive patients had lower PSA response rates than AR-V7-negative patients (0% vs. 53%, P=0.004) and shorter PSA progression-free survival (median, 1.4 months vs. 6.0 months; P<0.001), clinical or radiographic progression-free survival (median, 2.1 months vs. 6.1 months; P<0.001), and overall survival (median, 5.5 months vs. not reached; P=0.002). Similarly, among men receiving abiraterone, AR-V7-positive patients had lower PSA response rates than AR-V7-negative patients (0% vs. 68%, P=0.004) and shorter PSA progression-free survival (median, 1.3 months vs. not reached; P<0.001), clinical or radiographic progression-free survival (median, 2.3 months vs. not reached; P<0.001), and overall survival (median, 10.6 months vs. not reached, P=0.006). The association between AR-V7 detection and therapeutic resistance was maintained after adjustment for expression of full-length androgen receptor messenger RNA.
Conclusions:
Detection of AR-V7 in circulating tumor cells from patients with castration-resistant prostate cancer may be associated with resistance to enzalutamide and abiraterone. These findings require large-scale prospective validation. (Funded by the Prostate Cancer Foundation and others.).
Insights
Detection of androgen receptor splice variant 7 (AR-V7) messenger RNA in circulating tumor cells indicates resistance to enzalutamide and abiraterone in advanced prostate cancer patients. This biomarker may predict treatment outcomes for castration-resistant prostate cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The androgen receptor (AR) splice variant 7 (AR-V7) lacks the ligand-binding domain, rendering it resistant to standard therapies like enzalutamide and abiraterone.
- Despite lacking the target domain, AR-V7 remains constitutively active as a transcription factor, driving tumor progression.
Purpose of the Study:
- To investigate the association between the presence of AR-V7 messenger RNA (AR-V7 mRNA) in circulating tumor cells (CTCs) and treatment resistance.
- To evaluate the clinical utility of AR-V7 detection as a predictive biomarker for response to enzalutamide and abiraterone in metastatic castration-resistant prostate cancer (mCRPC).
Main Methods:
- A quantitative reverse-transcriptase-polymerase-chain-reaction (RT-PCR) assay was employed to detect AR-V7 mRNA in CTCs.
- Patients with mCRPC initiating treatment with enzalutamide or abiraterone were prospectively enrolled.
- Associations between AR-V7 status and outcomes including prostate-specific antigen (PSA) response, PSA progression-free survival (PFS), clinical/radiographic PFS, and overall survival (OS) were analyzed.
Main Results:
- AR-V7 mRNA was detected in 39% of enzalutamide-treated and 19% of abiraterone-treated patients.
- AR-V7-positive patients showed significantly lower PSA response rates (0% vs. 53% for enzalutamide, 0% vs. 68% for abiraterone) and shorter PFS and OS compared to AR-V7-negative patients.
- The association between AR-V7 detection and therapeutic resistance persisted even after adjusting for full-length AR mRNA expression.
Conclusions:
- Detection of AR-V7 in CTCs is associated with resistance to enzalutamide and abiraterone in patients with castration-resistant prostate cancer.
- AR-V7 may serve as a valuable predictive biomarker for guiding treatment decisions in mCRPC.
- Large-scale prospective validation studies are warranted to confirm these findings.
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