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首页> 外文期刊>BMC Urology >Impact of hormonal therapy on the detection of promoter hypermethylation of the detoxifying glutathione-S-transferase P1 gene (GSTP1) in prostate cancer
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Impact of hormonal therapy on the detection of promoter hypermethylation of the detoxifying glutathione-S-transferase P1 gene (GSTP1) in prostate cancer

机译:激素治疗对前列腺癌排毒谷胱甘肽-S-转移酶P1基因(GSTP1)启动子高甲基化检测的影响

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Background In spite of excellent cure rates for prostate cancer patients with favorable tumor characteristics, patients with unfavorable characteristics after radical prostatectomy are still at a significantly increased risk of tumor progression. Early adjuvant hormonal therapy (AHT) has been shown to be of prognostic benefit in these patients. Unfortunately initiation and duration of early AHT in the individual patient is based on statistic data. PSA, as the standard prostate marker is neither able to reliably indicate minimal residual tumor disease in the early postoperative phase, nor can it be used for therapy monitoring due to the suppressive effect of hormonal therapy on PSA production. Promoter hypermethylation of the detoxifying glutathione-S-transferase P1 gene (GSTP1-HM) has been shown to be the most common DNA alteration of primary prostatic carcinoma which, when used as a marker, is supposed to be able to overcome some of the disadvantages of PSA. However until now information on the impact of hormonal therapy on the detection of GSTP1-HM is lacking. The purpose of our study was to assess the impact of endocrine therapy on the detection of GSTP1-HM by methylation-specific PCR (MSP) in prostate cancer. Methods Paraffin embedded tumor samples from the radical prostatectomy (RP) specimens from 15 patients after hormonal therapy (HT) (mean 8 months) were assessed by MSP. In 8 of the patients the GSTP-1 status of the tumors before HT was assessed on the corresponding initial diagnostic biopsies. Results Following HT MSP showed GSTP1-HM in 13/15 of the RP specimens. In two patients analysis of the RP specimens failed to show GSTP1-HM. All initial tumor samples (8/8 biopsy specimens) showed GSTP1-HM, including both patients negative for GSTP1 HM in the corresponding RP specimen. Conclusion In most cases hormonal therapy appears to not alter GSTP1 HM detection. However the change from a positive to a negative GSTP1 HM status in a subset of the patients may point to an, at least partial androgen dependency. Further studies on a larger cohort of patients are necessary to assess its frequency and the exact hormonal interactions.
机译:背景技术尽管对于具有良好肿瘤特征的前列腺癌患者,治愈率极高,但是在前列腺癌根治术后具有不良特征的患者仍然明显增加了肿瘤进展的风险。早期辅助激素治疗(AHT)已显示出对这些患者的预后益处。不幸的是,单个患者早期AHT的发生和持续时间是基于统计数据的。 PSA作为标准的前列腺标记物,既不能可靠地指示术后早期的残留肿瘤最小,又由于激素治疗对PSA产生的抑制作用而不能用于治疗监测。排毒的谷胱甘肽-S-转移酶P1基因(GSTP1-HM)的启动子高甲基化已被证明是原发性前列腺癌最常见的DNA改变,当用作标志物时,它有望克服某些缺点PSA。然而,到目前为止,还缺乏关于激素治疗对GSTP1-HM检测的影响的信息。我们研究的目的是评估内分泌治疗对前列腺癌中甲基化特异性PCR(MSP)检测GSTP1-HM的影响。方法采用MSP评估15例激素治疗(HT)患者(平均8个月)根治性前列腺切除术(RP)标本中石蜡包埋的肿瘤标本。在8位患者中,通过相应的初始诊断活检评估了HT前肿瘤的GSTP-1状态。 HT MSP后的结果在RP标本的13/15中显示GSTP1-HM。在两名患者中,RP标本的分析未能显示GSTP1-HM。所有初始肿瘤样本(8/8活检标本)均显示GSTP1-HM,包括在相应的RP标本中均对GSTP1 HM阴性的两名患者。结论在大多数情况下,激素治疗似乎不会改变GSTP1 HM的检测。但是,在一部分患者中,GSTP1 HM状态从阳性变为阴性可能表示至少部分雄激素依赖性。为了评估其频率和确切的激素相互作用,有必要对更大范围的患者进行进一步研究。

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