Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.
Department of Pathology, Institute of Urology, West People's Republic of China Hospital, Sichuan University, Chengdu, Sichuan, People's Republic of China.
Oncologist. 2022 Nov 3;27(11):e870-e877. doi: 10.1093/oncolo/oyac177.
Aldo-keto reductase family 1 member C3 (AKR1C3) is important in prostate cancer progression, being a potential biomarker in metastatic castration-resistant prostate cancer (mCRPC). Previous explorations of AKR1C3 are mainly based on tissue samples. This study investigates using plasma-based liquid biopsy to validate the prognostic and predictive value of AKR1C3 in patients with mCRPC .
We prospectively recruited 62 patients with mCRPC. All patients received repeated prostate biopsies at the time of mCRPC diagnosis, and immunohistochemistry (IHC) staining was used to detect protein expression of AKR1C3 in the tissues. We took their blood simultaneously and performed digital droplet polymerase chain reaction (ddPCR) to measure expression levels of AKR1C3 in the exosomes. The detected plasma and tissue AKR1C3 expression levels were analyzed for patients' overall survival (OS) and progression-free survival under first-line abiraterone use (ABI-PFS).
All other baseline characteristics were balanced between the 2 groups. 15/62 (24.2%) and 25/62 (40.3%) patients showed AKR1C3-EXO positive (≥20 copies/20 μL) and AKR1C3-IHC positive, respectively. Positive AKR1C3-EXO expression was associated with decreased patients' survival [ABI-PFS: 3.9 vs 10.1 months, P < .001; OS: 16.2 vs 32.5 months, P < .001]. AKR1C3-IHC positivity was also correlated with ABI-PFS and OS (P = .010, P = .016). In patients with worse baseline blood tests (including higher alkaline phosphatase (ALP) and lactate dehydrogenase (LDH) level and lower hemoglobin (HB) level), and lower ISUP/WHO group (<4), their OS was significantly worse when showing AKR1C3-EXO positive.
AKR1C3-EXO is associated with patient prognosis regarding OS and ABI-PFS and can be used as a biomarker in mCRPC.
醛酮还原酶家族 1 成员 C3(AKR1C3)在前列腺癌进展中很重要,是转移性去势抵抗性前列腺癌(mCRPC)的潜在生物标志物。以前对 AKR1C3 的探索主要基于组织样本。本研究通过使用基于血浆的液体活检来验证 AKR1C3 在 mCRPC 患者中的预后和预测价值。
我们前瞻性招募了 62 例 mCRPC 患者。所有患者在诊断为 mCRPC 时均接受了重复的前列腺活检,并使用免疫组织化学(IHC)染色检测组织中 AKR1C3 的蛋白表达。同时采集他们的血液并进行数字液滴聚合酶链反应(ddPCR)以测量外泌体中 AKR1C3 的表达水平。分析检测到的血浆和组织 AKR1C3 表达水平,以评估一线阿比特龙使用(ABI-PFS)下患者的总生存期(OS)和无进展生存期。
两组之间的所有其他基线特征均平衡。62 例患者中,15 例(24.2%)和 25 例(40.3%)患者的 AKR1C3-EXO 表达阳性(≥20 拷贝/20 μL)和 AKR1C3-IHC 阳性。阳性 AKR1C3-EXO 表达与患者生存时间缩短相关[ABI-PFS:3.9 与 10.1 个月,P<0.001;OS:16.2 与 32.5 个月,P<0.001]。AKR1C3-IHC 阳性也与 ABI-PFS 和 OS 相关(P=0.010,P=0.016)。在基线血液检查较差的患者(包括较高的碱性磷酸酶(ALP)和乳酸脱氢酶(LDH)水平以及较低的血红蛋白(HB)水平)和较低的 ISUP/WHO 组(<4)中,当 AKR1C3-EXO 阳性时,其 OS 明显更差。
AKR1C3-EXO 与 OS 和 ABI-PFS 患者的预后相关,可作为 mCRPC 的生物标志物。