• 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

锌和锌转运体在前列腺癌发生中的作用。

Zinc and zinc transporters in prostate carcinogenesis.

机构信息

Fox Chase Cancer Center, Department of Surgical Oncology, Philadelphia, PA 19111-2497, USA.

出版信息

Nat Rev Urol. 2013 Apr;10(4):219-26. doi: 10.1038/nrurol.2013.43. Epub 2013 Mar 12.

DOI:10.1038/nrurol.2013.43
PMID:23478540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3702371/
Abstract

The healthy human prostate accumulates the highest level of zinc of any soft tissue in the body. This unique property is retained in BPH, but is lost in prostatic malignancy, which implicates changes in zinc and its transporters in carcinogenesis. Indeed, zinc concentrations diminish early in the course of prostate carcinogenesis, preceding histopathological changes, and continue to decline during progression toward castration-resistant disease. Numerous studies suggest that increased zinc intake might protect against progression of prostatic malignancy. In spite of increased dietary intake, zinc accumulation might be limited by the diminished expression of zinc uptake transporters, resulting in decreased intratumoural zinc levels. This finding can explain the conflicting results of various epidemiological studies evaluating the role of zinc supplementation on primary and secondary prostate cancer prevention. Overall, more research into the mechanisms of zinc homeostasis are needed to fully understand its impact on prostate carcinogenesis. Only then can the potential of zinc and zinc transport proteins be harnessed in the diagnosis and treatment of men with prostate cancer.

摘要

健康男性的前列腺组织是人体所有软组织中含锌量最高的。这一独特特性在 BPH 中得以保留,但在前列腺恶性肿瘤中却消失了,这表明锌及其转运蛋白的变化与癌症的发生有关。事实上,锌浓度在前列腺癌发生的早期就会降低,早于组织病理学改变,并且在向去势抵抗性疾病进展的过程中继续下降。许多研究表明,增加锌的摄入可能有助于预防前列腺恶性肿瘤的进展。尽管膳食摄入增加,但锌的积累可能会受到锌摄取转运体表达减少的限制,从而导致肿瘤内锌水平降低。这一发现可以解释评估锌补充剂对原发性和继发性前列腺癌预防作用的各种流行病学研究结果相互矛盾的原因。总的来说,需要进一步研究锌动态平衡的机制,以充分了解其对前列腺癌发生的影响。只有这样,才能利用锌和锌转运蛋白的潜力,用于诊断和治疗患有前列腺癌的男性。

相似文献

1
Zinc and zinc transporters in prostate carcinogenesis.锌和锌转运体在前列腺癌发生中的作用。
Nat Rev Urol. 2013 Apr;10(4):219-26. doi: 10.1038/nrurol.2013.43. Epub 2013 Mar 12.
2
Zinc and zinc transporters in normal prostate and the pathogenesis of prostate cancer.正常前列腺中的锌及锌转运体与前列腺癌的发病机制
Front Biosci. 2005 Sep 1;10:2230-9. doi: 10.2741/1692.
3
Dietary Phytochemicals in Zinc Homeostasis: A Strategy for Prostate Cancer Management.锌稳态中的膳食植物化学物质:前列腺癌管理策略
Nutrients. 2021 May 30;13(6):1867. doi: 10.3390/nu13061867.
4
hZIP1 zinc uptake transporter down regulation and zinc depletion in prostate cancer.hZIP1锌摄取转运体下调与前列腺癌中的锌耗竭
Mol Cancer. 2005 Sep 9;4:32. doi: 10.1186/1476-4598-4-32.
5
Evidence for a zinc uptake transporter in human prostate cancer cells which is regulated by prolactin and testosterone.人前列腺癌细胞中存在一种锌摄取转运体的证据,该转运体受催乳素和睾酮调节。
J Biol Chem. 1999 Jun 18;274(25):17499-504. doi: 10.1074/jbc.274.25.17499.
6
Resveratrol-zinc combination for prostate cancer management.白藜芦醇-锌联合用于前列腺癌治疗
Cell Cycle. 2014;13(12):1867-74. doi: 10.4161/cc.29334. Epub 2014 May 27.
7
Insight to physiology and pathology of zinc(II) ions and their actions in breast and prostate carcinoma.锌(II)离子在乳腺癌和前列腺癌中的生理学和病理学作用及其机制研究进展。
Curr Med Chem. 2011;18(33):5041-51. doi: 10.2174/092986711797636126.
8
hZip2 and hZip3 zinc transporters are down regulated in human prostate adenocarcinomatous glands.hZip2和hZip3锌转运体在人前列腺腺癌腺体内表达下调。
Mol Cancer. 2007 Jun 5;6:37. doi: 10.1186/1476-4598-6-37.
9
Novel role of zinc in the regulation of prostate citrate metabolism and its implications in prostate cancer.锌在前列腺柠檬酸代谢调节中的新作用及其对前列腺癌的影响
Prostate. 1998 Jun 1;35(4):285-96. doi: 10.1002/(sici)1097-0045(19980601)35:4<285::aid-pros8>3.0.co;2-f.
10
Reversal of epigenetic silencing of AP-2alpha results in increased zinc uptake in DU-145 and LNCaP prostate cancer cells.表观遗传沉默的 AP-2alpha 的逆转导致 DU-145 和 LNCaP 前列腺癌细胞中锌摄取的增加。
Carcinogenesis. 2011 Dec;32(12):1773-81. doi: 10.1093/carcin/bgr212. Epub 2011 Sep 22.

引用本文的文献

1
Temporal GeneTerrain: advancing precision medicine through dynamic gene expression visualization.时间基因图谱:通过动态基因表达可视化推动精准医学发展。
Front Bioinform. 2025 Jun 18;5:1602850. doi: 10.3389/fbinf.2025.1602850. eCollection 2025.
2
Spatial integration of multi-omics data from serial sections using the novel Multi-Omics Imaging Integration Toolset.使用新型多组学成像整合工具集对连续切片的多组学数据进行空间整合。
Gigascience. 2025 Jan 6;14. doi: 10.1093/gigascience/giaf035.
3
Piperazine-Based Co(III), Ni(II), Cu(II), and Zn(II) Carbodithioate Complexes as Potential Anticancer Agent.

本文引用的文献

1
Serum zinc and prostate cancer risk in a nested case-control study: The multiethnic cohort.血清锌与前列腺癌风险的巢式病例对照研究:多民族队列研究。
Prostate. 2013 Feb 15;73(3):261-6. doi: 10.1002/pros.22565. Epub 2012 Jul 31.
2
Novel Polypyridyl chelators deplete cellular zinc and destabilize the X-linked inhibitor of apoptosis protein (XIAP) prior to induction of apoptosis in human prostate and breast cancer cells.新型多吡啶螯合剂在诱导人前列腺和乳腺癌细胞凋亡之前会耗竭细胞内锌并使 X 连锁凋亡抑制蛋白(XIAP)失稳。
J Cell Biochem. 2012 Aug;113(8):2567-75. doi: 10.1002/jcb.24132.
3
Cytotoxic/tumor suppressor role of zinc for the treatment of cancer: an enigma and an opportunity.
基于哌嗪的二硫代碳酸钴(III)、镍(II)、铜(II)和锌(II)配合物作为潜在抗癌剂
ACS Omega. 2025 Apr 1;10(14):13829-13838. doi: 10.1021/acsomega.4c06972. eCollection 2025 Apr 15.
4
Dextran-Graft-Polyacrylamide/Zinc Oxide Nanoparticles Inhibit of Cancer Cells in vitro and in vivo.葡聚糖接枝聚丙烯酰胺/氧化锌纳米粒子在体外和体内抑制癌细胞。
Int J Nanomedicine. 2024 Nov 11;19:11719-11743. doi: 10.2147/IJN.S485106. eCollection 2024.
5
Zinc ions activate AKT and promote prostate cancer cell proliferation via disrupting AKT intramolecular interaction.锌离子通过破坏AKT分子内相互作用来激活AKT并促进前列腺癌细胞增殖。
Oncogene. 2025 Jan;44(1):8-18. doi: 10.1038/s41388-024-03195-x. Epub 2024 Oct 23.
6
Synthesis, characterization, and crystal structure of hexa-kis-(1-methyl-1-imidazole-κ )zinc(II) dinitrate.六 - 双 -(1 - 甲基 - 1 - 咪唑 - κ)硝酸锌(II)的合成、表征及晶体结构
Acta Crystallogr E Crystallogr Commun. 2024 Sep 24;80(Pt 10):1054-1058. doi: 10.1107/S2056989024008806. eCollection 2024 Sep 1.
7
Organoselenium transition metal complexes as promising candidates in medicine area.有机硒过渡金属配合物作为有前途的医学领域候选物。
J Biol Inorg Chem. 2024 Sep;29(6):555-571. doi: 10.1007/s00775-024-02072-y. Epub 2024 Aug 9.
8
Structural investigations and antibacterial, antifungal and anticancer studies on zinc salicylaldimine complexes.锌水杨醛亚胺配合物的结构研究及抗菌、抗真菌和抗癌研究。
Future Med Chem. 2024 Aug 2;16(15):1551-1560. doi: 10.1080/17568919.2024.2363672. Epub 2024 Jun 20.
9
Modeling Zinc Complexes Using Neural Networks.使用神经网络对锌配合物进行建模。
J Chem Inf Model. 2024 Apr 22;64(8):3140-3148. doi: 10.1021/acs.jcim.4c00095. Epub 2024 Apr 8.
10
A prognostic and immune related risk model based on zinc homeostasis in hepatocellular carcinoma.基于肝细胞癌锌稳态的预后及免疫相关风险模型
iScience. 2024 Mar 2;27(4):109389. doi: 10.1016/j.isci.2024.109389. eCollection 2024 Apr 19.
锌在癌症治疗中的细胞毒性/肿瘤抑制作用:一个谜和一个机会。
Expert Rev Anticancer Ther. 2012 Jan;12(1):121-8. doi: 10.1586/era.11.190.
4
Zinc and human health: an update.锌与人类健康:最新研究进展。
Arch Toxicol. 2012 Apr;86(4):521-34. doi: 10.1007/s00204-011-0775-1. Epub 2011 Nov 10.
5
miR-183-96-182 cluster is overexpressed in prostate tissue and regulates zinc homeostasis in prostate cells.miR-183-96-182 簇在前列腺组织中过表达,并调节前列腺细胞中的锌稳态。
J Biol Chem. 2011 Dec 30;286(52):44503-11. doi: 10.1074/jbc.M111.262915. Epub 2011 Nov 1.
6
Reversal of epigenetic silencing of AP-2alpha results in increased zinc uptake in DU-145 and LNCaP prostate cancer cells.表观遗传沉默的 AP-2alpha 的逆转导致 DU-145 和 LNCaP 前列腺癌细胞中锌摄取的增加。
Carcinogenesis. 2011 Dec;32(12):1773-81. doi: 10.1093/carcin/bgr212. Epub 2011 Sep 22.
7
Protective effect of zinc on N-methyl-N-nitrosourea and testosterone-induced prostatic intraepithelial neoplasia in the dorsolateral prostate of Sprague Dawley rats.锌对 N-甲基-N-亚硝脲和睾酮诱导的 Sprague Dawley 大鼠背外侧前列腺上皮内瘤形成的保护作用。
Exp Biol Med (Maywood). 2011 Sep;236(9):1012-21. doi: 10.1258/ebm.2011.010392. Epub 2011 Aug 24.
8
The role of zinc transporter ZIP4 in prostate carcinoma.锌转运蛋白 ZIP4 在前列腺癌中的作用。
Urol Oncol. 2012 Nov-Dec;30(6):906-11. doi: 10.1016/j.urolonc.2010.11.010. Epub 2011 Jul 30.
9
Zinc status of patients with benign prostatic hyperplasia and prostate carcinoma.良性前列腺增生症和前列腺癌患者的锌状态
Indian J Urol. 2011 Jan;27(1):14-8. doi: 10.4103/0970-1591.78405.
10
A null-mutation in the Znt7 gene accelerates prostate tumor formation in a transgenic adenocarcinoma mouse prostate model.Znt7 基因的无突变加速了转基因腺癌小鼠前列腺模型中的前列腺肿瘤形成。
Cancer Lett. 2011 Sep 1;308(1):33-42. doi: 10.1016/j.canlet.2011.04.011. Epub 2011 May 28.