Department of Urology, Xuzhou Cancer Hospital, Affiliated Xuzhou Hospital of Jiangsu University, Xuzhou, Jiangsu, China (mainland).
Department of Urology, Chinese PLA General Hospital, Beijing, China (mainland).
Med Sci Monit. 2017 Oct 13;23:4895-4900. doi: 10.12659/msm.904366.
BACKGROUND PCDH8 is a newly-discovered suppressor gene that is frequently inactivated by aberrant methylation in several human cancers, including prostate cancer. The identification of PCDH8 methylation can be used as a potential predictive biomarker. Prostate cancer patients with high Gleason score are considered as being at high risk for tumor recurrence and progression, and adjuvant therapy is often routinely performed in clinical practice. In the present study, we did not measure the methylation of PCDH8 in these patients. The main purpose of the present study was to evaluate the clinical significance of PCDH8 methylation in serum of prostate cancer patients with low Gleason score. MATERIAL AND METHODS PCDH8 methylation in serum samples of 117 patients and 47 controls was checked by methylation-specific PCR (MSP). Then, we correlated PCDH8 methylation status with the clinicopathological parameters of prostate cancer patients with low Gleason score and patient outcomes. RESULTS We found that PCDH8 was more frequently methylated in serum samples of patients with prostate cancer than in controls. PCDH8 methylation was correlated with advanced clinical stage (P=0.021), higher level of preoperative PSA (P=0.008), and positive lymph node metastasis (P=0.010). Moreover, patients with PCDH8 methylation had worse biochemical recurrence (BCR)-free survival (P<0.001) than patients without. Independent prognostic factors for worse BCR-free survival of prostate cancer patients with low Gleason score were: PCDH8 methylation in serum (Exp (B)=3.147, 95% CI: 1.152-7.961, P=0.007), clinical stage (Exp (B)=2.53, 95% CI: 1.032-4.763, P=0.025) and lymph node status (Exp (B)=1.476, 95% CI: 1.107-4.572, P=0.042). CONCLUSIONS Our study indicated that PCDH8 methylation in serum occurred frequently in prostate cancer patients and was correlated with risk factors for poor outcome. The methylation of PCDH8 in serum is a potential predictive marker for prostate cancer patients with low Gleason score after surgery.
PCDH8 是一种新发现的抑癌基因,在包括前列腺癌在内的多种人类癌症中常因异常甲基化而失活。PCDH8 甲基化的鉴定可作为潜在的预测生物标志物。高格里森评分的前列腺癌患者被认为有肿瘤复发和进展的高风险,因此在临床实践中常常规进行辅助治疗。在本研究中,我们没有测量这些患者的 PCDH8 甲基化。本研究的主要目的是评估低格里森评分前列腺癌患者血清中 PCDH8 甲基化的临床意义。
采用甲基化特异性 PCR(MSP)检测 117 例患者和 47 例对照者血清中 PCDH8 的甲基化情况。然后,我们将 PCDH8 甲基化状态与低格里森评分前列腺癌患者的临床病理参数和患者预后相关联。
我们发现,与对照组相比,前列腺癌患者血清中 PCDH8 的甲基化更为频繁。PCDH8 甲基化与晚期临床分期(P=0.021)、术前 PSA 水平较高(P=0.008)和淋巴结阳性转移(P=0.010)相关。此外,PCDH8 甲基化的患者生化无复发生存率(BCR)更差(P<0.001)。低格里森评分前列腺癌患者 BCR 无复发生存不良的独立预后因素为:血清中 PCDH8 甲基化(Exp(B)=3.147,95%CI:1.152-7.961,P=0.007)、临床分期(Exp(B)=2.53,95%CI:1.032-4.763,P=0.025)和淋巴结状态(Exp(B)=1.476,95%CI:1.107-4.572,P=0.042)。
本研究表明,前列腺癌患者血清中 PCDH8 甲基化发生率较高,与不良预后的危险因素相关。血清中 PCDH8 的甲基化是低格里森评分前列腺癌患者术后的潜在预测标志物。