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. 2022 Aug 10;20:119. doi: 10.1186/s12964-022-00925-0

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — TNC and AR-V7 expression decrease in 3D heterotypical organoids treated with testosterone. A and B Effect of testosterone (1 nM), estradiol (10 nM), and enzalutamide (10 µM) on TNC, AR-V7, AR-FL, and Kallikrein related peptidase 3 (KLK3)/ Prostate Specific antigen (PSA) in 3D prostate cancer (VCaP or 22Rv1) and heterotypical (VCaP-22Rv1/MC3T3-E1) organoids using RT-qPCR. Human-specific primers were used for RT-qPCR to exclude transcripts from mouse derived preosteoblasts (MC3T3-E1). All data represent mean ± SD analyzed by unpaired students t-test (n = 3) *p < 0.05; ** p < 0.01; ***p < 0.001; ****p < 0.0001