期刊文献+

基于醛酮还原酶1C3的抗肿瘤药物研究进展

Advances in Research on Antitumor Drugs Based on Aldo-keto Reductase 1C3
原文传递
导出
摘要 醛酮还原酶(aldo-keto reductase,AKR)1C3是AKR超家族的成员之一,在多种恶性实体瘤和血液肿瘤细胞中的表达水平高于正常细胞,并与癌症的发生和发展以及肿瘤对化疗/免疫疗法的耐药性和对放疗的抵抗性密切相关。研究已证明,AKR1C3既可以作为生物标志物,用于肿瘤病人筛选、指导用药和预后诊断,也可作为抗肿瘤药物的新靶标,用于药物设计和研发。基于AKR1C3的抗肿瘤药物有望为临床用药提供新的解决方案。回顾了近年来基于AKR1C3的抗肿瘤药物的研究进展,并对该研究领域进行了展望。 Aldo-keto reductase(AKR)1C3 is a member of the AKR superfamily.Its expression level in a variety of malignant solid tumor cells and hematologic tumor cells is higher than that in normal cells,which is closely related to the occurrence and development of cancer,as well as tumor resistance to chemotherapy/immunotherapy and resistance to radiotherapy.Studies have proved that AKRIC3 can be used both as a biomarker for screening,drug guidance and prognostic diagnosis of tumor patients,and as a new target of anti-tumor drugs for drug design and development.Anti-tumor drugs based on AKRIC3 are expected to provide novel solutions for clinical use.In this article,the research progress of anti-tumor drugs based on AKRIC3 in rcent years has been reviewed,and an outlook of the research field has been provided.
作者 卢兆强 段建新 孟繁英 李安蓉 LU Zhaoqiang;DUAN Jianxin;MENG Fanying;LI Anrong(Ascentawits Pharmaceuticals,Ltd,Shenzhen 518118.China)
出处 《药学进展》 CAS 2023年第3期164-178,共15页 Progress in Pharmaceutical Sciences
关键词 醛酮还原酶1C3 生物标志物 靶向抗肿瘤药物 前药 活化 aldo-keto reductase 1C3 biomarker targeted anti.tumor drug prodrug activation
  • 相关文献

参考文献4

二级参考文献40

  • 1Jie Ju,An-Jie Zhu,Peng Yuan.Progress in targeted therapy for breast cancer[J].Chronic Diseases and Translational Medicine,2018,4(3):164-175. 被引量:4
  • 2Prokai-Tatrai K,Perjesi P,Zharikova AD,et al.Design, synthesis and biological evaluation of novel, centrally-acting thyrotropin-releasing hormone analogues[].Bioorg Med ChemLett.2002 被引量:1
  • 3Lucer US.Fosphenytoin[].Neurological Research.1998 被引量:1
  • 4Mavon A,Raufast V,Redoules D.Skin absorption and metabolism of a new vitamin E prodrug, δ-tocopherol-glucoside: in vitro evaluation in human skin models[].Journal of Controlled Release.2004 被引量:1
  • 5Curini M,Epifano F,Genovese S.Synthesis of a novel prodrug of 3-(4-geranyloxy-3-methoxyphenyl)-2-trans-propenoic acid for colon delivery[].Bioorganic and Medicinal Chemistry.2005 被引量:1
  • 6Naka T,Kubo Y,Nishikawa K,et al.A New class of diacidic nonpeptide angiotensin Ⅱ receptor antagonists: Candesartan cilexetil[].Drug Des Discov.1999 被引量:1
  • 7Xi MM,Zhang SQ,Wang XY,et al.Study on the characteristics of pectin-ketoprofen for colon targeting in rats[].International Journal of Pharmaceutics.2005 被引量:1
  • 8Stella VJ,Himmelstein KJ.Prodrugs and site-specific drug delivery[].Journal of Medicinal Chemistry.1980 被引量:1
  • 9Yano H,Hirayama F,Arima H.Preparation of prednisolone appended alpha, beta and gamma cyclodextrins: substitution at secondary hydroxyl groups and in vitro hydrolysis behavior[].Journal of Pharmacological Sciences.2001 被引量:1
  • 10Patel K,Trivedi S,Luo S,et al.Synthesis, physicochemical properties and antiviral activities of ester prodrugs of ganciclovir[].International Journal of Pharmaceutics.2005 被引量:1

共引文献23

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部