Literature DB >> 16185154

Targeted treatment of cancer with artemisinin and artemisinin-tagged iron-carrying compounds.

Henry Lai1, Tomikazu Sasaki, Narendra P Singh.   

Abstract

Artemisinin is a chemical compound that reacts with iron to form free radicals which can kill cells. Cancer cells require and uptake a large amount of iron to proliferate. They are more susceptible to the cytotoxic effect of artemisinin than normal cells. Cancer cells express a large concentration of cell surface transferrin receptors that facilitate uptake of the plasma iron-carrying protein transferrin via endocytosis. By covalently tagging artemisinin to transferrin, artemisinin could be selectively picked up and concentrated by cancer cells. Futhermore, both artemisinin and iron would be transported into the cell in one package. Once an artemisinin-tagged transferrin molecule is endocytosed, iron is released and reacts with artemisinin moieties tagged to transferrin. Formation of free radicals kills the cancer cell. The authors have found that artemisinin-tagged transferrin is highly selective and potent in killing cancer cells. Thus, artemisinin and artemisinin-tagged iron-carrying compounds could be developed into powerful anticancer drugs.

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Year:  2005        PMID: 16185154     DOI: 10.1517/14728222.9.5.995

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  16 in total

1.  Design, synthesis, and study of a mycobactin-artemisinin conjugate that has selective and potent activity against tuberculosis and malaria.

Authors:  Marvin J Miller; Andrew J Walz; Helen Zhu; Chunrui Wu; Garrett Moraski; Ute Möllmann; Esther M Tristani; Alvin L Crumbliss; Michael T Ferdig; Lisa Checkley; Rachel L Edwards; Helena I Boshoff
Journal:  J Am Chem Soc       Date:  2011-01-28       Impact factor: 15.419

Review 2.  Necroptosis: A new way of dying?

Authors:  Britt Hanson
Journal:  Cancer Biol Ther       Date:  2016-07-19       Impact factor: 4.742

3.  Artemisinin: A Promising Adjunct for Cancer Therapy.

Authors:  Yamna Waseem; Choudhary A Hasan; Furqan Ahmed
Journal:  Cureus       Date:  2018-11-23

Review 4.  Development of artemisinin compounds for cancer treatment.

Authors:  Henry C Lai; Narendra P Singh; Tomikazu Sasaki
Journal:  Invest New Drugs       Date:  2012-08-31       Impact factor: 3.850

Review 5.  The transferrin receptor and the targeted delivery of therapeutic agents against cancer.

Authors:  Tracy R Daniels; Ezequiel Bernabeu; José A Rodríguez; Shabnum Patel; Maggie Kozman; Diego A Chiappetta; Eggehard Holler; Julia Y Ljubimova; Gustavo Helguera; Manuel L Penichet
Journal:  Biochim Biophys Acta       Date:  2011-08-05

6.  Malaria-infected mice are cured by a single oral dose of new dimeric trioxane sulfones which are also selectively and powerfully cytotoxic to cancer cells.

Authors:  Andrew S Rosenthal; Xiaochun Chen; Jun O Liu; Diana C West; Paul J Hergenrother; Theresa A Shapiro; Gary H Posner
Journal:  J Med Chem       Date:  2009-02-26       Impact factor: 7.446

7.  Effect of artemisinins and other endoperoxides on nitric oxide-related signaling pathway in RAW 264.7 mouse macrophage cells.

Authors:  V Badireenath Konkimalla; Martina Blunder; Bernhard Korn; Shahid A Soomro; Herwig Jansen; Wonsuk Chang; Gary H Posner; Rudolf Bauer; Thomas Efferth
Journal:  Nitric Oxide       Date:  2008-04-22       Impact factor: 4.427

Review 8.  Antitumor activity of artemisinin and its derivatives: from a well-known antimalarial agent to a potential anticancer drug.

Authors:  Maria P Crespo-Ortiz; Ming Q Wei
Journal:  J Biomed Biotechnol       Date:  2011-11-22

Review 9.  Anticancer Effect of AntiMalarial Artemisinin Compounds.

Authors:  A K Das
Journal:  Ann Med Health Sci Res       Date:  2015 Mar-Apr

10.  Compounds Derived from the Bhutanese Daisy, Ajania nubigena, Demonstrate Dual Anthelmintic Activity against Schistosoma mansoni and Trichuris muris.

Authors:  Phurpa Wangchuk; Mark S Pearson; Paul R Giacomin; Luke Becker; Javier Sotillo; Darren Pickering; Michael J Smout; Alex Loukas
Journal:  PLoS Negl Trop Dis       Date:  2016-08-04
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