Literature DB >> 16356830

Oral artemisinin prevents and delays the development of 7,12-dimethylbenz[a]anthracene (DMBA)-induced breast cancer in the rat.

Henry Lai1, Narendra P Singh.   

Abstract

Artemisinin, a compound isolated from the sweet wormwood Artemisia annua L., has previously been shown to have selective toxicity towards cancer cells in vitro. In the present experiment, we studied the potential of artemisinin to prevent breast cancer development in rats treated with a single oral dose (50mg/kg) of 7,12-dimethylbenz[a]anthracene (DMBA), known to induce multiple breast tumors. Starting from the day immediately after DMBA treatment, one group of rats was provided with a powdered rat-chow containing 0.02% artemisinin, whereas a control group was provided with plain powdered food. For 40 weeks, both groups of rats were monitored for breast tumors. Oral artemisinin significantly delayed (P<.002) and in some animals prevented (57% of artemisinin-fed versus 96% of the controls developed tumors, P<.01) breast cancer development in the monitoring period. In addition, breast tumors in artemisinin-fed rats were significantly fewer (P<.002) and smaller in size (P<.05) when compared with controls. Since artemisinin is a relatively safe compound that causes no known side effects even at high oral doses, the present data indicate that artemisinin may be a potent cancer-chemoprevention agent.

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Year:  2006        PMID: 16356830     DOI: 10.1016/j.canlet.2005.01.019

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  35 in total

1.  Effects of nanoliposomal and pegylated nanoliposomal artemisinin in treatment of breast cancer.

Authors:  Neda Dadgar; Maedeh Koohi Moftakhari Esfahani; Sepideh Torabi; Seyed Ebrahim Alavi; Azim Akbarzadeh
Journal:  Indian J Clin Biochem       Date:  2013-10-01

2.  Artesunate inhibits cell proliferation and decreases growth hormone synthesis and secretion in GH3 cells.

Authors:  Zhi-Gang Mao; Jing Zhou; Hui Wang; Dong-Sheng He; Wei-Wei Xiao; Gui-Zhi Liao; Lu-Bin Qiu; Yong-Hong Zhu; Hai-Jun Wang
Journal:  Mol Biol Rep       Date:  2012-01-05       Impact factor: 2.316

3.  pH-responsive artemisinin dimer in lipid nanoparticles are effective against human breast cancer in a xenograft model.

Authors:  Yitong J Zhang; Xi Zhan; Liguo Wang; Rodney J Y Ho; Tomikazu Sasaki
Journal:  J Pharm Sci       Date:  2015-03-09       Impact factor: 3.534

4.  Anti-tumor effects of dihydroartemisinin on human osteosarcoma.

Authors:  Ye Ji; Yi-Cai Zhang; Liu-Bao Pei; Li-Li Shi; Jing-Long Yan; Xue-Hua Ma
Journal:  Mol Cell Biochem       Date:  2011-01-14       Impact factor: 3.396

5.  Artemisinin reduces human melanoma cell migration by down-regulating alpha V beta 3 integrin and reducing metalloproteinase 2 production.

Authors:  Elisabetta Buommino; Adone Baroni; Nunzia Canozo; Marcella Petrazzuolo; Rosario Nicoletti; Antonio Vozza; Maria Antonietta Tufano
Journal:  Invest New Drugs       Date:  2008-10-28       Impact factor: 3.850

6.  Artemisinin selectively decreases functional levels of estrogen receptor-alpha and ablates estrogen-induced proliferation in human breast cancer cells.

Authors:  Shyam N Sundar; Crystal N Marconett; Victor B Doan; Jamin A Willoughby; Gary L Firestone
Journal:  Carcinogenesis       Date:  2008-09-10       Impact factor: 4.944

Review 7.  Redox-directed cancer therapeutics: molecular mechanisms and opportunities.

Authors:  Georg T Wondrak
Journal:  Antioxid Redox Signal       Date:  2009-12       Impact factor: 8.401

8.  Study of toxicity effect of pegylated nanoliposomal artemisinin on breast cancer cell line.

Authors:  Neda Dadgar; Seyed Ebrahim Alavi; Maedeh Koohi Moftakhari Esfahani; Azim Akbarzadeh
Journal:  Indian J Clin Biochem       Date:  2013-02-10

9.  Dihydroartemisinin (DHA) induces caspase-3-dependent apoptosis in human lung adenocarcinoma ASTC-a-1 cells.

Authors:  Ying-Ying Lu; Tong-Sheng Chen; Jun-Le Qu; Wen-Liang Pan; Lei Sun; Xun-Bin Wei
Journal:  J Biomed Sci       Date:  2009-02-02       Impact factor: 8.410

10.  Heme mediates cytotoxicity from artemisinin and serves as a general anti-proliferation target.

Authors:  Shiming Zhang; Glenn S Gerhard
Journal:  PLoS One       Date:  2009-10-28       Impact factor: 3.240

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