• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

使用Gleason评分,研究前列腺癌侵袭性与雄激素剥夺治疗前后前列腺中二氢睾酮水平的变化。

The change in the dihydrotestosterone level in the prostate before and after androgen deprivation therapy in connection with prostate cancer aggressiveness using the Gleason score.

作者信息

Nishiyama Tsutomu, Ikarashi Toshihiko, Hashimoto Yutaka, Wako Koichi, Takahashi Kota

机构信息

Division of Urology, Department of Regenerative and Transplant Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

出版信息

J Urol. 2007 Oct;178(4 Pt 1):1282-8; discussion 1288-9. doi: 10.1016/j.juro.2007.05.138. Epub 2007 Aug 14.

DOI:10.1016/j.juro.2007.05.138
PMID:17698092
Abstract

PURPOSE

We investigated the change in dihydrotestosterone in the prostate during androgen deprivation therapy in connection with prostate cancer aggressiveness using the Gleason score.

MATERIALS AND METHODS

A total of 28 patients with clinically localized prostate cancer who were treated with androgen deprivation therapy for 6 months were enrolled in this study. Dihydrotestosterone in the prostate and serum were analyzed using liquid chromatography/electrospray ionization-mass spectrometry after polar derivatization before and after androgen deprivation therapy.

RESULTS

The change in dihydrotestosterone during androgen deprivation therapy in the prostate with Gleason score 7 to 10 prostate cancer was significantly smaller than that in the prostate with Gleason score 6 or less (p = 0.016). There were no significant differences between patients with Gleason score 7 to 10 prostate cancer and patients with Gleason score 6 or less in dihydrotestosterone in the prostate, in serum androgens and in serum androgen ratios before and after androgen deprivation therapy.

CONCLUSIONS

Low dihydrotestosterone in the prostate is probably sufficient to propagate the growth of aggressive prostate cancer. Furthermore, the prostate with aggressive prostate cancer can produce androgens from adrenal precursors more autonomously than the prostate with nonaggressive prostate cancer under a low testosterone environment with testicular suppression.

摘要

目的

我们使用Gleason评分研究了去势治疗期间前列腺中双氢睾酮的变化与前列腺癌侵袭性之间的关系。

材料与方法

本研究共纳入28例接受6个月去势治疗的临床局限性前列腺癌患者。在去势治疗前后,采用液相色谱/电喷雾电离-质谱法对前列腺和血清中的双氢睾酮进行极性衍生化分析。

结果

Gleason评分为7至10分的前列腺癌患者在去势治疗期间前列腺中双氢睾酮的变化明显小于Gleason评分为6分或更低的患者(p = 0.016)。Gleason评分为7至10分的前列腺癌患者与Gleason评分为6分或更低的患者在去势治疗前后前列腺中的双氢睾酮、血清雄激素及血清雄激素比值方面均无显著差异。

结论

前列腺中低水平的双氢睾酮可能足以促进侵袭性前列腺癌的生长。此外,在睾丸抑制导致睾酮水平较低的环境下,侵袭性前列腺癌的前列腺比非侵袭性前列腺癌的前列腺能更自主地从肾上腺前体产生雄激素。

相似文献

1
The change in the dihydrotestosterone level in the prostate before and after androgen deprivation therapy in connection with prostate cancer aggressiveness using the Gleason score.使用Gleason评分,研究前列腺癌侵袭性与雄激素剥夺治疗前后前列腺中二氢睾酮水平的变化。
J Urol. 2007 Oct;178(4 Pt 1):1282-8; discussion 1288-9. doi: 10.1016/j.juro.2007.05.138. Epub 2007 Aug 14.
2
Association between the dihydrotestosterone level in the prostate and prostate cancer aggressiveness using the Gleason score.利用Gleason评分评估前列腺中双氢睾酮水平与前列腺癌侵袭性之间的关联。
J Urol. 2006 Oct;176(4 Pt 1):1387-91. doi: 10.1016/j.juro.2006.06.066.
3
Serum prostate-specific antigen levels reflect the androgen milieu in patients with localized prostate cancer receiving androgen deprivation therapy: Tumor malignant potential and androgen milieu.血清前列腺特异性抗原水平反映接受雄激素剥夺治疗的局限性前列腺癌患者的雄激素环境:肿瘤恶性潜能与雄激素环境。
Prostate. 2010 Sep 15;70(13):1395-401. doi: 10.1002/pros.21174.
4
The influence of androgen deprivation therapy on dihydrotestosterone levels in the prostatic tissue of patients with prostate cancer.雄激素剥夺疗法对前列腺癌患者前列腺组织中二氢睾酮水平的影响。
Clin Cancer Res. 2004 Nov 1;10(21):7121-6. doi: 10.1158/1078-0432.CCR-04-0913.
5
Redefining clinically significant castration levels in patients with prostate cancer receiving continuous androgen deprivation therapy.重新定义接受持续雄激素剥夺治疗的前列腺癌患者具有临床意义的去势水平。
J Urol. 2007 Oct;178(4 Pt 1):1290-5. doi: 10.1016/j.juro.2007.05.129. Epub 2007 Aug 14.
6
Adrenocorticotropic hormone is involved in regulation of androgen synthesis in men receiving androgen deprivation therapy for localized prostate cancer.促肾上腺皮质激素参与接受雄激素剥夺治疗局限性前列腺癌男性雄激素合成的调节。
J Urol. 2010 Nov;184(5):1971-6. doi: 10.1016/j.juro.2010.06.115.
7
The effects of combined androgen blockade on cognitive function during the first cycle of intermittent androgen suppression in patients with prostate cancer.联合雄激素阻断对前列腺癌患者间歇性雄激素抑制首个周期认知功能的影响。
J Urol. 2003 Nov;170(5):1808-11. doi: 10.1097/01.ju.0000091640.59812.83.
8
Immunomagnetic quantification of circulating tumor cells as a prognostic factor of androgen deprivation responsiveness in patients with hormone naive metastatic prostate cancer.循环肿瘤细胞的免疫磁珠定量分析作为激素初治转移性前列腺癌患者雄激素剥夺反应性的预后因素
J Urol. 2008 Oct;180(4):1342-7. doi: 10.1016/j.juro.2008.06.021. Epub 2008 Aug 15.
9
Adrenal androgen levels as predictors of outcome in castration-resistant prostate cancer patients treated with combined androgen blockade using flutamide as a second-line anti-androgen.使用氟他胺作为二线抗雄激素药物的联合雄激素阻断治疗的去势抵抗性前列腺癌患者,肾上腺雄激素水平作为预后的预测指标。
Int J Urol. 2010 Apr;17(4):337-45. doi: 10.1111/j.1442-2042.2010.02473.x. Epub 2010 Mar 1.
10
Finnish multicenter study comparing intermittent to continuous androgen deprivation for advanced prostate cancer: interim analysis of prognostic markers affecting initial response to androgen deprivation.芬兰多中心研究:比较晚期前列腺癌间歇性雄激素剥夺疗法与持续性雄激素剥夺疗法——影响雄激素剥夺初始反应的预后标志物的中期分析
J Urol. 2008 Sep;180(3):915-9; discussion 919-20. doi: 10.1016/j.juro.2008.05.009. Epub 2008 Jul 17.

引用本文的文献

1
The Predictive Role of the Gleason Score in Determining Prognosis to Systematic Treatment in Metastatic Castration-Sensitive Prostate Cancer: A Systematic Review and Network Meta-Analysis.Gleason评分在转移性去势敏感性前列腺癌系统治疗预后判定中的预测作用:一项系统评价与网状Meta分析
J Clin Med. 2025 Feb 17;14(4):1326. doi: 10.3390/jcm14041326.
2
Side effects of prostate cancer therapies and potential management.前列腺癌治疗的副作用及潜在管理方法。
J Biol Methods. 2024 Aug 22;11(3):e99010018. doi: 10.14440/jbm.2024.0019. eCollection 2024.
3
Histone H2A Lys130 acetylation epigenetically regulates androgen production in prostate cancer.
组蛋白 H2A 赖氨酸 130 乙酰化通过表观遗传调控前列腺癌细胞中的雄激素生成。
Nat Commun. 2023 Jun 9;14(1):3357. doi: 10.1038/s41467-023-38887-7.
4
Tautomycin and enzalutamide combination yields synergistic effects on castration-resistant prostate cancer.曲古抑菌素和恩杂鲁胺联合使用对去势抵抗性前列腺癌产生协同作用。
Cell Death Discov. 2022 Nov 29;8(1):471. doi: 10.1038/s41420-022-01257-1.
5
Advances in the Current Understanding of the Mechanisms Governing the Acquisition of Castration-Resistant Prostate Cancer.去势抵抗性前列腺癌获得机制的当前理解进展
Cancers (Basel). 2022 Jul 31;14(15):3744. doi: 10.3390/cancers14153744.
6
Association of prostate cancer SLCO gene expression with Gleason grade and alterations following androgen deprivation therapy.前列腺癌 SLCO 基因表达与 Gleason 分级及去势治疗后改变的相关性研究。
Prostate Cancer Prostatic Dis. 2019 Dec;22(4):560-568. doi: 10.1038/s41391-019-0141-6. Epub 2019 Mar 19.
7
Adrenal androgens rescue prostatic dihydrotestosterone production and growth of prostate cancer cells after castration.去势后肾上腺雄激素可挽救前列腺细胞中二氢睾酮的产生和生长。
Mol Cell Endocrinol. 2019 Apr 15;486:79-88. doi: 10.1016/j.mce.2019.02.018. Epub 2019 Feb 23.
8
Classical and Non-Classical Roles for Pre-Receptor Control of DHT Metabolism in Prostate Cancer Progression.双氢睾酮代谢的受体前调控在前列腺癌进展中的经典与非经典作用
Horm Cancer. 2016 Apr;7(2):104-13. doi: 10.1007/s12672-016-0250-9. Epub 2016 Jan 21.
9
Topologically inferring pathway activity toward precise cancer classification via integrating genomic and metabolomic data: prostate cancer as a case.通过整合基因组和代谢组数据进行拓扑学推断通路活性以实现精确的癌症分类:以前列腺癌为例
Sci Rep. 2015 Aug 19;5:13192. doi: 10.1038/srep13192.
10
Steroid hormone synthetic pathways in prostate cancer.前列腺癌中的类固醇激素合成途径。
Transl Androl Urol. 2013 Sep;2(3):212-227. doi: 10.3978/j.issn.2223-4683.2013.09.16.