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抗激素治疗可调节 LNCaP 细胞中 PSA 的分泌、PSMA 的表达和 Ga-PSMA 的摄取。

Antihormone treatment differentially regulates PSA secretion, PSMA expression and Ga-PSMA uptake in LNCaP cells.

机构信息

Department of Nuclear Medicine, University Hospital Bonn, Venusberg Campus 1, 53127, Bonn, Germany.

Department of Pathology, University Hospital Bonn, Venusberg Campus 1, 53127, Bonn, Germany.

出版信息

J Cancer Res Clin Oncol. 2021 Jun;147(6):1733-1743. doi: 10.1007/s00432-021-03583-w. Epub 2021 Mar 24.

Abstract

BACKGROUND

In recent years, a variety of innovative therapeutics for castration-resistant prostate cancer have been developed, including novel anti-androgenic drugs, such as abiraterone or VPC-13566. Therapeutic monitoring of these pharmaceuticals is performed either by measuring PSA levels in serum or by imaging. PET using PSMA ligands labeled with Fluor-18 or Gallium-68 is the most sensitive and specific imaging modality for detection of metastases in advanced prostate cancer. To date, it remains unclear how PSMA expression is modulated by anti-hormonal treatment and how it correlates with PSA secretion.

METHODS

We analyzed modulation of PSMA-mRNA and protein expression, Ga-PSMA uptake and regulation of PSA secretion by abiraterone or VPC-13566 in LNCaP cells in vitro.

RESULTS

We found that abiraterone and VPC-13566 upregulate PSMA protein and mRNA expression but block PSA secretion in LNCaP cells. Both anti-androgens also enhanced Ga-PSMA uptake normalized by the number of cells, whereas abiraterone and VPC-13566 reduced Ga-PSMA uptake in total LNCaP monolayers treated due to cell death.

CONCLUSION

Our data indicate that PSA secretion and PSMA expression are differentially regulated upon anti-androgen treatment. This finding might be important for the interpretation of Ga-PSMA PET images in monitoring therapies with abiraterone and VPC-13566 in prostate cancer patients, but needs to be validated in vivo.

摘要

背景

近年来,已经开发出了多种用于治疗去势抵抗性前列腺癌的创新疗法,包括新型抗雄激素药物,如阿比特龙或 VPC-13566。这些药物的治疗监测通过测量血清中的 PSA 水平或通过成像进行。使用 PSMA 配体标记氟-18 或镓-68 的 PET 是检测晚期前列腺癌转移的最敏感和最特异的成像方式。迄今为止,尚不清楚抗激素治疗如何调节 PSMA 表达,以及它与 PSA 分泌的相关性如何。

方法

我们分析了 PSMA-mRNA 和蛋白表达、Ga-PSMA 摄取以及阿比特龙或 VPC-13566 在体外 LNCaP 细胞中对 PSA 分泌的调节。

结果

我们发现阿比特龙和 VPC-13566 上调了 LNCaP 细胞中 PSMA 蛋白和 mRNA 表达,但阻断了 PSA 的分泌。两种抗雄激素药物也增强了 Ga-PSMA 的摄取,通过细胞数量进行了归一化,而阿比特龙和 VPC-13566 减少了由于细胞死亡而在整个 LNCaP 单层中处理的 Ga-PSMA 摄取。

结论

我们的数据表明,PSA 分泌和 PSMA 表达在抗雄激素治疗时受到不同的调节。这一发现可能对解释使用阿比特龙和 VPC-13566 监测前列腺癌患者治疗的 Ga-PSMA PET 图像具有重要意义,但需要在体内进行验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46cf/11802094/363c17115ac4/432_2021_3583_Fig1_HTML.jpg

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