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©The Author(s) 2022.
World J Clin Cases. Apr 16, 2022; 10(11): 3461-3471
Published online Apr 16, 2022. doi: 10.12998/wjcc.v10.i11.3461
Published online Apr 16, 2022. doi: 10.12998/wjcc.v10.i11.3461
Figure 2 Circulating tumor cells and dynamic change of serum total prostate-specific antigen level.
A: Dynamic change of serum total prostate-specific antigen level during the overall treatment with various therapeutic approaches (androgen-deprivation therapy; docetaxel; abiraterone; clinical trial; the PARP inhibitor, olaparib); B: The epithelial-circulating tumor cell (E-CTC), mesenchymal-CTC (M-CTC) and epithelial mesenchymal transition-CTC (EMT-CTC) counts and change before (2017-06-13) and after (2018-06-19) abiraterone treatment. Expression of AR-V7 mRNA was detected in these CTCs; C: Representative graphs displaying the E-CTC, M-CTC and EMT-CTC. Red signal: Probe mixture for detection of mRNA of EpCAM, CK8, CK18, and CK19; Green signal: Probe mixture for detection of mRNA of vimentin and Twist. CTC: Circulating tumor cell.
- Citation: Yuan F, Liu N, Yang MZ, Zhang XT, Luo H, Zhou H. Circulating tumor DNA genomic profiling reveals the complicated olaparib-resistance mechanism in prostate cancer salvage therapy: A case report. World J Clin Cases 2022; 10(11): 3461-3471
- URL: https://www.wjgnet.com/2307-8960/full/v10/i11/3461.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v10.i11.3461