• 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

膀胱癌靶向治疗的新型药物

Emerging drugs for targeted therapy of bladder cancer.

作者信息

Agarwal Piyush K, Black Peter C, McConkey David J, Dinney Colin P N

机构信息

Department of Urology, University of Texas, MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Expert Opin Emerg Drugs. 2007 Sep;12(3):435-48. doi: 10.1517/14728214.12.3.435.

DOI:10.1517/14728214.12.3.435
PMID:17874971
Abstract

Although chemotherapy has improved the treatment of metastatic bladder cancer, resection and continual surveillance remain the modalities used for treatment of organ-confined disease. More targeted therapies are needed to address the shortcomings of existing treatments. The authors recently became aware of the overexpression of tyrosine kinase growth factor receptors in a variety of malignancies. These receptor tyrosine kinases are coupled to several proliferative and antiapoptotic pathways that drive cancer cell growth. Targeted small-molecule therapies, including monoclonal antibodies and tyrosine kinase inhibitors, directed at these receptors have proven effective against a variety of tumor models. In this report, the authors summarize the results of several such studies and discuss the rationale and potential use of novel targeted drugs in the treatment of bladder cancer.

摘要

尽管化疗改善了转移性膀胱癌的治疗,但手术切除和持续监测仍是治疗器官局限性疾病的常用方法。需要更多靶向治疗来弥补现有治疗方法的不足。作者最近意识到酪氨酸激酶生长因子受体在多种恶性肿瘤中过度表达。这些受体酪氨酸激酶与多种驱动癌细胞生长的增殖和抗凋亡途径相关联。针对这些受体的靶向小分子疗法,包括单克隆抗体和酪氨酸激酶抑制剂,已被证明对多种肿瘤模型有效。在本报告中,作者总结了几项此类研究的结果,并讨论了新型靶向药物治疗膀胱癌的理论依据和潜在用途。

相似文献

1
Emerging drugs for targeted therapy of bladder cancer.膀胱癌靶向治疗的新型药物
Expert Opin Emerg Drugs. 2007 Sep;12(3):435-48. doi: 10.1517/14728214.12.3.435.
2
Emerging drugs for non-small-cell lung cancer.非小细胞肺癌的新型药物
Expert Opin Emerg Drugs. 2007 Sep;12(3):449-60. doi: 10.1517/14728214.12.3.449.
3
Tyrosine kinase receptor inhibitor-targeted combined chemotherapy for metastatic bladder cancer.酪氨酸激酶受体抑制剂靶向联合化疗治疗转移性膀胱癌。
Kaohsiung J Med Sci. 2012 Apr;28(4):194-203. doi: 10.1016/j.kjms.2011.06.020. Epub 2011 Sep 25.
4
Biomarker targets and novel therapeutics.生物标志物靶点与新型疗法。
Cancer Treat Res. 2009;149:85-105. doi: 10.1007/978-0-387-98094-2_4.
5
Novel agents, combinations and sequences for the treatment of advanced renal cell carcinoma: When is the revolution coming?新型药物、联合用药及治疗方案在晚期肾细胞癌中的应用:革命何时到来?
Curr Cancer Drug Targets. 2013 Mar;13(3):313-25. doi: 10.2174/1568009611313030009.
6
Targeting non-receptor tyrosine kinases using small molecule inhibitors: an overview of recent advances.使用小分子抑制剂靶向非受体酪氨酸激酶:近期进展综述
J Drug Target. 2016;24(3):192-211. doi: 10.3109/1061186X.2015.1068319. Epub 2015 Jul 27.
7
Sunitinib enhances antitumor effects against chemotherapy-resistant bladder cancer through suppression of ERK1/2 phosphorylation.舒尼替尼通过抑制 ERK1/2 磷酸化增强对抗化疗耐药性膀胱癌的抗肿瘤作用。
Int J Oncol. 2012 May;40(5):1691-6. doi: 10.3892/ijo.2012.1368. Epub 2012 Feb 13.
8
Oligonucleotide aptamers against tyrosine kinase receptors: Prospect for anticancer applications.针对酪氨酸激酶受体的寡核苷酸适体:在抗癌应用方面的前景。
Biochim Biophys Acta Rev Cancer. 2018 Apr;1869(2):263-277. doi: 10.1016/j.bbcan.2018.03.003. Epub 2018 Mar 21.
9
Novel approaches with targeted therapies in bladder cancer. Therapy of bladder cancer by blockade of the epidermal growth factor receptor family.膀胱癌靶向治疗的新方法。通过阻断表皮生长因子受体家族治疗膀胱癌。
Crit Rev Oncol Hematol. 2003 Jun 27;46 Suppl:S85-104. doi: 10.1016/s1040-8428(03)00067-2.
10
Targeted therapies in bladder cancer--an update.膀胱癌的靶向治疗——最新进展
Urol Oncol. 2007 Sep-Oct;25(5):433-8. doi: 10.1016/j.urolonc.2007.05.011.

引用本文的文献

1
Role of tyrosine kinases in bladder cancer progression: an overview.酪氨酸激酶在膀胱癌进展中的作用:概述。
Cell Commun Signal. 2020 Aug 14;18(1):127. doi: 10.1186/s12964-020-00625-7.
2
FGFR3b Extracellular Loop Mutation Lacks Tumorigenicity In Vivo but Collaborates with p53/pRB Deficiency to Induce High-grade Papillary Urothelial Carcinoma.FGFR3b细胞外环突变在体内缺乏致瘤性,但与p53/pRB缺陷协同作用可诱导高级别乳头状尿路上皮癌。
Sci Rep. 2016 May 9;6:25596. doi: 10.1038/srep25596.
3
miR-200 expression regulates epithelial-to-mesenchymal transition in bladder cancer cells and reverses resistance to epidermal growth factor receptor therapy.
微小RNA-200的表达调控膀胱癌细胞的上皮-间质转化,并逆转对表皮生长因子受体疗法的耐药性。
Clin Cancer Res. 2009 Aug 15;15(16):5060-72. doi: 10.1158/1078-0432.CCR-08-2245. Epub 2009 Aug 11.