• 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

Transferrin directed delivery of adriamycin to human cells.

作者信息

Singh M, Atwal H, Micetich R

机构信息

College of Pharmacy, Florida A and M University, Tallahassee 32307, USA.

出版信息

Anticancer Res. 1998 May-Jun;18(3A):1423-7.

PMID:9673350
Abstract

Transferrin was covalently conjugated to adriamycin (Trf-adr) by the formation of a schiff base. This conjugate was found to bind to cell membrane trf receptors in a variety of human tumor cell lines. The Trf-adr conjugate was found to be active against sensitive and resistant cell lines e.g. Lovo, HL-60, H-meso and Hep2. It was, however, found that Trf-adr conjugate was more potent against resistant human tumor cell lines as compared to sensitive cell lines (based on cytotoxicity assays). The Trf-adr conjugate was then tested against nude mice bearing human mesothelioma tumors in their peritoneal cavity. The Trf-adr conjugate prolonged the lifespan of advanced tumor bearing nude mice as compared to either adriamycin alone or adriamycin and trf unlinked. Our studies show that trf can be successfully used as an ligand for directing anticancer drugs to human tumor cells.

摘要

相似文献

1
Transferrin directed delivery of adriamycin to human cells.
Anticancer Res. 1998 May-Jun;18(3A):1423-7.
2
Adriamycin conjugates of human transferrin bind transferrin receptors and kill K562 and HL60 cells.人转铁蛋白的阿霉素缀合物可结合转铁蛋白受体并杀死K562和HL60细胞。
Arch Biochem Biophys. 1993 Jan;300(1):356-63. doi: 10.1006/abbi.1993.1048.
3
Sensitivity of multidrug-resistant MCF-7 cells to a transferrin-doxorubicin conjugate.多药耐药性MCF - 7细胞对转铁蛋白 - 阿霉素偶联物的敏感性
Anticancer Res. 1994 Mar-Apr;14(2A):397-403.
4
[Experimental study on targeting therapy of human hepatocellular carcinoma in nude mice using adriamycin-anti-transferrin receptor conjugate].
Zhonghua Zhong Liu Za Zhi. 1995 Sep;17(5):354-7.
5
Transferrin as a drug carrier: Cytotoxicity, cellular uptake and transport kinetics of doxorubicin transferrin conjugate in the human leukemia cells.转铁蛋白作为药物载体:阿霉素-转铁蛋白缀合物在人白血病细胞中的细胞毒性、细胞摄取和转运动力学。
Toxicol In Vitro. 2014 Mar;28(2):187-97. doi: 10.1016/j.tiv.2013.09.013. Epub 2013 Sep 19.
6
Tumor regression after systemic administration of tocotrienol entrapped in tumor-targeted vesicles.系统给予生育三烯酚包封于肿瘤靶向囊泡后的肿瘤消退。
J Control Release. 2009 Dec 3;140(2):95-9. doi: 10.1016/j.jconrel.2009.08.017. Epub 2009 Aug 23.
7
Targeted adriamycin delivery to MXT-B2 metastatic mammary carcinoma cells by transferrin liposomes: effect of adriamycin ADR-to-lipid ratio.通过转铁蛋白脂质体将阿霉素靶向递送至MXT-B2转移性乳腺癌细胞:阿霉素(ADR)与脂质比例的影响
Oncol Rep. 2005 Nov;14(5):1337-43.
8
Adriamycin sensitizes the adriamycin-resistant 8226/Dox40 human multiple myeloma cells to Apo2L/tumor necrosis factor-related apoptosis-inducing ligand-mediated (TRAIL) apoptosis.阿霉素使耐阿霉素的8226/Dox40人多发性骨髓瘤细胞对Apo2L/肿瘤坏死因子相关凋亡诱导配体介导的(TRAIL)凋亡敏感。
Clin Cancer Res. 2001 Dec;7(12):3874-83.
9
Transferrin conjugates of adriamycin are cytotoxic without intercalating nuclear DNA.阿霉素的转铁蛋白缀合物具有细胞毒性,但不会嵌入核DNA。
J Biol Chem. 1992 May 5;267(13):9437-42.
10
Enhancement of murine tumor cell sensitivity to adriamycin by presentation of the drug in phosphatidylcholine-phosphatidylserine liposomes.
Cancer Res. 1990 Jun 15;50(12):3619-26.

引用本文的文献

1
Pathophysiological aspects of transferrin-A potential nano-based drug delivery signaling molecule in therapeutic target for varied diseases.转铁蛋白的病理生理学方面——一种潜在的基于纳米的药物递送信号分子,用于多种疾病的治疗靶点
Front Pharmacol. 2024 Mar 4;15:1342181. doi: 10.3389/fphar.2024.1342181. eCollection 2024.
2
Multi-Targeted Anticancer Activity of Imidazolate Phosphane Gold(I) Compounds by Inhibition of DHFR and TrxR in Breast Cancer Cells.咪唑膦金(I)化合物通过抑制乳腺癌细胞中的二氢叶酸还原酶和硫氧还蛋白还原酶发挥多靶点抗癌活性。
Front Chem. 2021 Jan 11;8:602845. doi: 10.3389/fchem.2020.602845. eCollection 2020.
3
Toward a magic or imaginary bullet? Ligands for drug targeting to cancer cells: principles, hopes, and challenges.
迈向神奇子弹还是虚构子弹?靶向癌细胞的药物配体:原理、希望与挑战。
Int J Nanomedicine. 2015 Feb 17;10:1399-414. doi: 10.2147/IJN.S74514. eCollection 2015.
4
Cellular uptake and internalization of hyaluronan-based doxorubicin and cisplatin conjugates.基于透明质酸的阿霉素和顺铂共轭物的细胞摄取与内化
J Drug Target. 2014 Aug;22(7):648-57. doi: 10.3109/1061186X.2014.921924. Epub 2014 Jun 3.
5
Transferrin receptor-mediated endocytosis: a useful target for cancer therapy.转铁蛋白受体介导的内吞作用:癌症治疗的一个有用靶点。
J Membr Biol. 2014 Apr;247(4):291-307. doi: 10.1007/s00232-014-9637-0. Epub 2014 Feb 27.
6
Nanotechnology and drug delivery: an update in oncology.纳米技术与药物输送:肿瘤学的最新进展。
Pharmaceutics. 2011 Apr 14;3(2):171-85. doi: 10.3390/pharmaceutics3020171.
7
Receptor-mediated endocytosis and brain delivery of therapeutic biologics.受体介导的内吞作用与治疗性生物制品的脑内递送
Int J Cell Biol. 2013;2013:703545. doi: 10.1155/2013/703545. Epub 2013 Jun 11.
8
PEG-transferrin conjugated TRAIL (TNF-related apoptosis-inducing ligand) for therapeutic tumor targeting.聚乙二醇-转铁蛋白偶联 TRAIL(肿瘤坏死因子相关凋亡诱导配体)用于治疗性肿瘤靶向。
J Control Release. 2012 Sep 10;162(2):422-8. doi: 10.1016/j.jconrel.2012.07.021. Epub 2012 Jul 21.
9
The transferrin receptor and the targeted delivery of therapeutic agents against cancer.转铁蛋白受体与抗癌治疗药物的靶向递送
Biochim Biophys Acta. 2012 Mar;1820(3):291-317. doi: 10.1016/j.bbagen.2011.07.016. Epub 2011 Aug 5.
10
Intracellular trafficking considerations in the development of natural ligand-drug molecular conjugates for cancer.在开发用于癌症的天然配体-药物分子偶联物时的细胞内转运考虑因素。
Ann Biomed Eng. 2011 Apr;39(4):1235-51. doi: 10.1007/s10439-011-0280-y. Epub 2011 Feb 25.