Department of Pathology and Laboratory Medicine, University of Wisconsin, Madison, WI 53792, USA.
Department of Urology, James Buchanan Brady Urological Institute, Johns Hopkins University, Baltimore, MD 21287, USA.
Hum Pathol. 2019 Feb;84:173-182. doi: 10.1016/j.humpath.2018.09.009. Epub 2018 Sep 26.
Androgen-deprivation therapy has been used to treat salivary duct carcinoma (SDC). The androgen receptor splice variant-7 (AR-V7) has been detected in castration-resistant prostate cancer and implicated in resistance to androgen receptor (AR)-targeted therapies. Given the potential role of AR/AR-V7 in SDC treatment, this study focuses on AR/AR-V7 expression in SDC specimens collected before androgen-deprivation therapy. RNA in situ hybridization (ISH) and immunohistochemistry (IHC) to detect total AR and AR-V7 were performed on formalin-fixed, paraffin-embedded SDC specimens from 23 patients. Full-length AR and AR-V7 transcripts were quantified in a subset of tumors by reverse-transcription polymerase chain reaction. Twenty SDCs were positive for total AR by ISH and IHC. Among AR-positive SDCs, 70% (14/20) were positive for AR-V7 messenger RNA by ISH, whereas 15% (3/20) were positive for AR-V7 protein by IHC. The 3 SDCs that expressed the highest levels of AR-V7 were all from female patients; one of them expressed a significant amount of AR-V7 and barely detectable full-length AR transcripts by reverse-transcription polymerase chain reaction. IHC expression of Forkhead box protein A1, prostate-specific antigen, prostatic acid phosphatase, and NKX3.1 was observed in some SDCs regardless of patient sex. Five SDCs demonstrated strong human epidermal growth factor receptor 2 expression. We conclude that treatment-naïve SDCs may express AR-V7 at levels comparable to or even exceeding the levels detected in castration-resistant prostate cancer. Our data support the feasibility to incorporate AR-V7 assessment via ISH and/or IHC in the ongoing clinical trials evaluating the therapeutic benefit of AR-targeted therapies in SDC patients.
雄激素剥夺疗法已被用于治疗唾液腺癌(SDC)。雄激素受体剪接变异体-7(AR-V7)已在去势抵抗性前列腺癌中被检测到,并与雄激素受体(AR)靶向治疗的耐药性有关。鉴于 AR/AR-V7 在 SDC 治疗中的潜在作用,本研究重点关注在接受雄激素剥夺治疗前收集的 SDC 标本中 AR/AR-V7 的表达。对 23 名患者的福尔马林固定、石蜡包埋的 SDC 标本进行了 RNA 原位杂交(ISH)和免疫组织化学(IHC)检测总 AR 和 AR-V7。在一部分肿瘤中通过逆转录聚合酶链反应定量全长 AR 和 AR-V7 转录本。20 例 SDC 通过 ISH 和 IHC 检测到总 AR 阳性。在 AR 阳性的 SDC 中,70%(14/20)通过 ISH 检测到 AR-V7 信使 RNA 阳性,而 15%(3/20)通过 IHC 检测到 AR-V7 蛋白阳性。3 例表达 AR-V7 水平最高的 SDC 均来自女性患者;其中 1 例通过逆转录聚合酶链反应检测到大量 AR-V7 和几乎检测不到全长 AR 转录本。一些 SDC 中观察到叉头框蛋白 A1、前列腺特异性抗原、前列腺酸性磷酸酶和 NKX3.1 的 IHC 表达,无论患者性别如何。5 例 SDC 表现出强烈的人表皮生长因子受体 2 表达。我们得出结论,未经治疗的 SDC 可能表达 AR-V7 的水平与甚至超过去势抵抗性前列腺癌中检测到的水平相当。我们的数据支持通过 ISH 和/或 IHC 纳入 AR-V7 评估的可行性,以评估 AR 靶向治疗在 SDC 患者中的治疗获益的正在进行的临床试验。