Department of Internal Medicine, Division of Metabolism, Endocrinology & Diabetes, University of Michigan, Ann Arbor, MI, USA.
Center for Public Health Genomics, University of Virginia, Charlottesville, VA, USA.
J Bone Miner Res. 2021 Aug;36(8):1566-1579. doi: 10.1002/jbmr.4313. Epub 2021 May 18.
Bone metastasis is a complication of prostate cancer in up to 90% of men afflicted with advanced disease. Therapies that reduce androgen exposure remain at the forefront of treatment. However, most prostate cancers transition to a state whereby reducing testicular androgen action becomes ineffective. A common mechanism of this transition is intratumoral production of testosterone (T) using the adrenal androgen precursor dehydroepiandrosterone (DHEA) through enzymatic conversion by 3β- and 17β-hydroxysteroid dehydrogenases (3βHSD and 17βHSD). Given the ability of prostate cancer to form blastic metastases in bone, we hypothesized that osteoblasts might be a source of androgen synthesis. RNA expression analyses of murine osteoblasts and human bone confirmed that at least one 3βHSD and 17βHSD enzyme isoform was expressed, suggesting that osteoblasts are capable of generating androgens from adrenal DHEA. Murine osteoblasts were treated with 100 nM and 1 μM DHEA or vehicle control. Conditioned media from these osteoblasts were assayed for intermediate and active androgens by liquid chromatography-tandem mass spectrometry. As DHEA was consumed, the androgen intermediates androstenediol and androstenedione were generated and subsequently converted to T. Conditioned media of DHEA-treated osteoblasts increased androgen receptor (AR) signaling, prostate-specific antigen (PSA) production, and cell numbers of the androgen-sensitive prostate cancer cell lines C4-2B and LNCaP. DHEA did not induce AR signaling in osteoblasts despite AR expression in this cell type. We describe an unreported function of osteoblasts as a source of T that is especially relevant during androgen-responsive metastatic prostate cancer invasion into bone. © 2021 American Society for Bone and Mineral Research (ASBMR). This article has been contributed to by US Government employees and their work is in the public domain in the USA.
骨转移是高达 90%患有晚期疾病的男性前列腺癌的并发症。减少雄激素暴露的治疗方法仍然是治疗的前沿。然而,大多数前列腺癌会转变为一种状态,即降低睾丸雄激素作用变得无效。这种转变的一个常见机制是通过 3β-和 17β-羟甾脱氢酶(3βHSD 和 17βHSD)的酶促转化,在肿瘤内使用肾上腺雄激素前体脱氢表雄酮(DHEA)产生睾酮(T)。鉴于前列腺癌在骨骼中形成成骨转移的能力,我们假设成骨细胞可能是雄激素合成的来源。对鼠成骨细胞和人骨的 RNA 表达分析证实,至少有一种 3βHSD 和 17βHSD 酶同工型表达,表明成骨细胞能够从肾上腺 DHEA 产生雄激素。用 100 nM 和 1 μM DHEA 或载体对照处理鼠成骨细胞。通过液相色谱-串联质谱法检测这些成骨细胞的条件培养基中的中间和活性雄激素。随着 DHEA 的消耗,雄激素中间体雄烯二酮和雄烯二酮被产生,随后转化为 T。用 DHEA 处理的成骨细胞的条件培养基增加了雄激素受体(AR)信号、前列腺特异性抗原(PSA)的产生和雄激素敏感的前列腺癌细胞系 C4-2B 和 LNCaP 的细胞数量。尽管在这种细胞类型中表达 AR,但 DHEA 并未诱导成骨细胞中的 AR 信号。我们描述了成骨细胞作为 T 源的一个未被报道的功能,这在雄激素反应性转移性前列腺癌侵入骨骼时尤其相关。© 2021 美国骨骼与矿物质研究协会(ASBMR)。本文已由美国政府雇员贡献,其工作在美国属于公有领域。