• 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

合成维甲酸类药物作为前列腺癌潜在治疗药物的研究进展:十年回顾。

Synthetic Retinoids as Potential Therapeutics in Prostate Cancer-An Update of the Last Decade of Research: A Review.

机构信息

Medical Biochemistry Medical College, Jagiellonian University, 31-034 Cracow, Poland.

Nutrition and Health Research Group 1 A-B, Department of Population Health, Luxembourg Institute of Health, 1 A-B, rue Thomas Edison, L-23 1445 Strassen, Luxembourg.

出版信息

Int J Mol Sci. 2021 Sep 29;22(19):10537. doi: 10.3390/ijms221910537.

DOI:10.3390/ijms221910537
PMID:34638876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8508817/
Abstract

Prostate cancer (PC) is the second most common tumor in males. The search for appropriate therapeutic options against advanced PC has been in process for several decades. Especially after cessation of the effectiveness of hormonal therapy (i.e., emergence of castration-resistant PC), PC management options have become scarce and the prognosis is poor. To overcome this stage of disease, an array of natural and synthetic substances underwent investigation. An interesting and promising class of compounds constitutes the derivatives of natural retinoids. Synthesized on the basis of the structure of retinoic acid, they present unique and remarkable properties that warrant their investigation as antitumor drugs. However, there is no up-to-date compilation that consecutively summarizes the current state of knowledge about synthetic retinoids with regard to PC. Therefore, in this review, we present the results of the experimental studies on synthetic retinoids conducted within the last decade. Our primary aim is to highlight the molecular targets of these compounds and to identify their potential promise in the treatment of PC.

摘要

前列腺癌(PC)是男性中第二常见的肿瘤。几十年来,人们一直在寻找针对晚期 PC 的合适治疗选择。特别是在激素治疗(即去势抵抗性 PC 的出现)失效后,PC 的治疗选择变得稀缺,预后较差。为了克服这一疾病阶段,大量的天然和合成物质接受了研究。一类有趣且有前途的化合物是天然视黄醇衍生物。它们是基于视黄酸的结构合成的,具有独特而显著的特性,这使其成为抗肿瘤药物的研究对象。然而,目前还没有最新的综述连续总结关于合成视黄醇在 PC 方面的最新知识状况。因此,在这篇综述中,我们展示了过去十年中关于合成视黄醇的实验研究结果。我们的主要目的是强调这些化合物的分子靶点,并确定它们在治疗 PC 方面的潜在前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e371/8508817/d5d237d87f57/ijms-22-10537-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e371/8508817/d5d237d87f57/ijms-22-10537-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e371/8508817/d5d237d87f57/ijms-22-10537-g001.jpg

相似文献

1
Synthetic Retinoids as Potential Therapeutics in Prostate Cancer-An Update of the Last Decade of Research: A Review.合成维甲酸类药物作为前列腺癌潜在治疗药物的研究进展:十年回顾。
Int J Mol Sci. 2021 Sep 29;22(19):10537. doi: 10.3390/ijms221910537.
2
Differential effects of synthetic nuclear retinoid receptor-selective retinoids on the growth of human non-small cell lung carcinoma cells.合成核类视黄醇受体选择性类视黄醇对人非小细胞肺癌细胞生长的差异效应。
Cancer Res. 1997 Nov 1;57(21):4931-9.
3
Receptor selective synthetic retinoids as potential cancer chemotherapy agents.受体选择性合成类视黄醇作为潜在的癌症化疗药物。
Curr Cancer Drug Targets. 2002 Mar;2(1):77-86. doi: 10.2174/1568009023333935.
4
Heterocycle-containing retinoids. Discovery of a novel isoxazole arotinoid possessing potent apoptotic activity in multidrug and drug-induced apoptosis-resistant cells.含杂环的类视黄醇。一种新型异恶唑类视黄醛的发现,其在多药耐药和药物诱导的凋亡抗性细胞中具有强大的凋亡活性。
J Med Chem. 2001 Jul 5;44(14):2308-18. doi: 10.1021/jm0010320.
5
Natural and synthetic retinoids in prostate cancer.前列腺癌中的天然和合成类视黄醇
Curr Pharm Des. 2006;12(15):1923-9. doi: 10.2174/138161206776873554.
6
Traffic lights for retinoids in oncology: molecular markers of retinoid resistance and sensitivity and their use in the management of cancer differentiation therapy.视黄醇在肿瘤学中的信号灯:视黄醇耐药性和敏感性的分子标志物及其在癌症分化治疗管理中的应用。
BMC Cancer. 2018 Nov 1;18(1):1059. doi: 10.1186/s12885-018-4966-5.
7
[Synthesis of retinoids with a modified polar group and their antitumor activity. Report I].[具有修饰极性基团的类视黄醇的合成及其抗肿瘤活性。报告一]
Bioorg Khim. 1995 Dec;21(12):941-9.
8
Effects of retinoid X receptor-selective ligands on proliferation of prostate cancer cells.维甲酸X受体选择性配体对前列腺癌细胞增殖的影响。
Prostate. 1997 Jul 1;32(2):115-21. doi: 10.1002/(sici)1097-0045(19970701)32:2<115::aid-pros6>3.0.co;2-l.
9
The emerging role of retinoids and retinoic acid metabolism blocking agents in the treatment of cancer.类视黄醇和视黄酸代谢阻断剂在癌症治疗中的新作用。
Cancer. 1998 Oct 15;83(8):1471-82. doi: 10.1002/(sici)1097-0142(19981015)83:8<1471::aid-cncr1>3.0.co;2-6.
10
Synthetic retinoid CD437 induces S-phase arrest and apoptosis in human prostate cancer cells LNCaP and PC-3.合成类视黄醇CD437可诱导人前列腺癌细胞LNCaP和PC-3发生S期阻滞和凋亡。
Prostate. 1999 Feb 15;38(3):228-36. doi: 10.1002/(sici)1097-0045(19990215)38:3<228::aid-pros7>3.0.co;2-t.

引用本文的文献

1
Aging, cancer, and autophagy: connections and therapeutic perspectives.衰老、癌症与自噬:关联及治疗前景
Front Mol Biosci. 2025 Jan 28;11:1516789. doi: 10.3389/fmolb.2024.1516789. eCollection 2024.
2
Attempts to Improve Lipophilic Drugs' Solubility and Bioavailability: A Focus on Fenretinide.提高亲脂性药物溶解度和生物利用度的尝试:以芬维A胺为重点。
Pharmaceutics. 2024 Apr 24;16(5):579. doi: 10.3390/pharmaceutics16050579.
3
Targeting lipid metabolism in metastatic prostate cancer.靶向转移性前列腺癌中的脂质代谢

本文引用的文献

1
Reply to Mrakic-Sposta et al. Comment on "Menzel et al. Common and Novel Markers for Measuring Inflammation and Oxidative Stress Ex Vivo in Research and Clinical Practice-Which to Use Regarding Disease Outcomes? 2021, , 414".对姆拉基奇 - 斯波斯塔等人的回复。关于“门泽尔等人。在研究和临床实践中用于体外测量炎症和氧化应激的常见和新型标志物——就疾病结局而言应使用哪些标志物?2021年,,414”的评论
Antioxidants (Basel). 2021 May 28;10(6):865. doi: 10.3390/antiox10060865.
2
Recent Progress in Discovering the Role of Carotenoids and Their Metabolites in Prostatic Physiology and Pathology with a Focus on Prostate Cancer-A Review-Part I: Molecular Mechanisms of Carotenoid Action.发现类胡萝卜素及其代谢产物在前列腺生理和病理中的作用的最新进展,重点关注前列腺癌——综述——第一部分:类胡萝卜素作用的分子机制
Antioxidants (Basel). 2021 Apr 10;10(4):585. doi: 10.3390/antiox10040585.
3
Ther Adv Med Oncol. 2023 Jan 30;15:17588359231152839. doi: 10.1177/17588359231152839. eCollection 2023.
4
Contribution of Cancer-Targeting Drugs toward Faster Clinical Application.癌症靶向药物对加速临床应用的贡献。
Int J Mol Sci. 2022 Jun 9;23(12):6445. doi: 10.3390/ijms23126445.
Recent Progress in Discovering the Role of Carotenoids and Metabolites in Prostatic Physiology and Pathology-A Review-Part II: Carotenoids in the Human Studies.发现类胡萝卜素及其代谢产物在前列腺生理和病理中的作用的最新进展——综述——第二部分:人体研究中的类胡萝卜素
Antioxidants (Basel). 2021 Feb 20;10(2):319. doi: 10.3390/antiox10020319.
4
The role of the retinoid receptor, RAR/RXR heterodimer, in liver physiology.视黄酸受体(RAR/RXR)异二聚体在肝脏生理中的作用。
Biochim Biophys Acta Mol Basis Dis. 2021 May 1;1867(5):166085. doi: 10.1016/j.bbadis.2021.166085. Epub 2021 Jan 24.
5
Ex Vivo Investigation of Bexarotene and Nicotinamide Function as a Protectıve Agent on Rat Synaptosomes Treated with Aβ(1-42).贝沙罗汀和烟酰胺对经β淀粉样蛋白(1-42)处理的大鼠突触体的保护作用的体外研究
Neurochem Res. 2021 Apr;46(4):804-818. doi: 10.1007/s11064-020-03216-7. Epub 2021 Jan 11.
6
Recent advances in the design of RAR α and RAR β agonists as orally bioavailable drugs. A review.新型 RARα 和 RARβ 激动剂的设计:口服生物利用度药物的进展。一篇综述。
Bioorg Med Chem. 2020 Oct 15;28(20):115664. doi: 10.1016/j.bmc.2020.115664. Epub 2020 Jul 29.
7
Disabling MNK protein kinases promotes oxidative metabolism and protects against diet-induced obesity.抑制 MNK 蛋白激酶可促进氧化代谢,预防饮食诱导的肥胖。
Mol Metab. 2020 Dec;42:101054. doi: 10.1016/j.molmet.2020.101054. Epub 2020 Jul 23.
8
Oxidative Stress and Antioxidant Status in High-Risk Prostate Cancer Subjects.高危前列腺癌患者的氧化应激与抗氧化状态
Diagnostics (Basel). 2020 Feb 27;10(3):126. doi: 10.3390/diagnostics10030126.
9
Understanding Failure and Improving Treatment Using HDAC Inhibitors for Prostate Cancer.了解前列腺癌治疗失败原因并利用组蛋白去乙酰化酶抑制剂改善治疗效果
Biomedicines. 2020 Jan 30;8(2):22. doi: 10.3390/biomedicines8020022.
10
Genomics of lethal prostate cancer at diagnosis and castration resistance.诊断时致命性前列腺癌和去势抵抗性前列腺癌的基因组学
J Clin Invest. 2020 Apr 1;130(4):1743-1751. doi: 10.1172/JCI132031.