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糖皮质激素受体在前列腺癌中的作用的叙述性综述:过去5年的进展

A narrative review of the role of glucocorticoid receptors in prostate cancer: developments in last 5 years.

作者信息

Zhou Feng, Shi Yue, Zhao Guan'an, Aufderklamm Stefan, Murray Katie S, Jin Baiye

机构信息

Department of Urology, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

Department of Urology, Eberhard-Karls University Tübingen, Tübingen, Germany.

出版信息

Transl Androl Urol. 2022 Aug;11(8):1189-1199. doi: 10.21037/tau-22-501.

Abstract

BACKGROUND AND OBJECTIVE

Glucocorticoids, secreted from the adrenal gland, are commonly used in the treatment of castration-resistant prostate cancer (CRPC) because of their anti-inflammatory and anti-toxic effects. However, glucocorticoids have been reported to have the opposite effects within the course of treatment. Many studies have shown that glucocorticoid receptors (GRs) are involved in the establishment of a dominant population of androgen-independent malignant cells, which may result in CRPC. In this review, we summarized the mechanisms of GRs in CRPC and the clinical application of glucocorticoids based on the present evidence.

METHODS

We summarized the isoforms of GRs and the mechanisms involved in CRPC. An updated literature search was performed from the ClinicalTrials database, the National Center for Biotechnology Information database and European Union Drug Regulating Authorities Clinical Trials database. The focus was on the timeframe from 2017 to 2022. At least one primary or secondary outcome [prostate-specific antigen (PSA) response rate, progression-free survival (PFS) or overall survival (OS) and median time to PSA progression] according to studies should be included.

KEY CONTENT AND FINDINGS

The molecular structures and applications of the isoforms of GR have been intensively researched in the past 60 years. In recent years, researchers have pointed out that GRs may be involved in the development of CRPC via genomic and non-genomic effects. Clinical trials in the past 5 years have focused on the efficacy of drugs regarding CRPC. The use of glucocorticoids during treatments of CRPC follows the guidelines (e.g., NCCN Guidelines, guidelines of CSCO, etc.). Based on the collected data, prednisone appears to be the most widely used steroid hormone, followed by dexamethasone. Comparisons of the PSA response rate and the median time to PSA progression revealed that the efficacy of the 2 hormones is similar; however, further research on the effect of steroid hormone in CRPC is still required.

CONCLUSIONS

Various GR isoforms may play an important part in the development of CRPC, whose mechanism remains unclear. Most clinical trials have focused on the use of prednisone in the last 5 years. The efficacy of prednisone and dexamethasone is similar.

摘要

背景与目的

肾上腺分泌的糖皮质激素因其抗炎和抗毒作用,常用于去势抵抗性前列腺癌(CRPC)的治疗。然而,有报道称糖皮质激素在治疗过程中会产生相反的作用。许多研究表明,糖皮质激素受体(GRs)参与雄激素非依赖性恶性细胞优势群体的形成,这可能导致CRPC。在本综述中,我们基于现有证据总结了GRs在CRPC中的作用机制以及糖皮质激素的临床应用。

方法

我们总结了GRs的亚型以及CRPC涉及的机制。从临床试验数据库、美国国立生物技术信息中心数据库和欧盟药品监管机构临床试验数据库进行了最新的文献检索。重点是2017年至2022年的时间段。根据研究应至少纳入一项主要或次要结局[前列腺特异性抗原(PSA)反应率、无进展生存期(PFS)或总生存期(OS)以及PSA进展的中位时间]。

关键内容与发现

在过去60年中,对GR亚型的分子结构和应用进行了深入研究。近年来,研究人员指出GRs可能通过基因组和非基因组效应参与CRPC的发展。过去5年的临床试验集中在药物对CRPC的疗效上。CRPC治疗期间糖皮质激素的使用遵循指南(如美国国立综合癌症网络指南、中国临床肿瘤学会指南等)。根据收集的数据,泼尼松似乎是使用最广泛的类固醇激素,其次是地塞米松。PSA反应率和PSA进展中位时间的比较显示,这两种激素的疗效相似;然而,仍需要对类固醇激素在CRPC中的作用进行进一步研究。

结论

各种GR亚型可能在CRPC的发展中起重要作用,其机制尚不清楚。在过去5年中,大多数临床试验集中在泼尼松的使用上。泼尼松和地塞米松的疗效相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc9d/9459548/6b21ac328538/tau-11-08-1189-f1.jpg

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