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Lectin of Concanavalin A As an Anti-hepatoma Therapeutic Agent

Overview
Journal J Biomed Sci
Publisher Biomed Central
Specialty Biology
Date 2009 Mar 11
PMID 19272170
Citations 34
Authors
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Abstract

Liver cancer is the predominant cause of cancer mortality in males of Southern China and Taiwan. The current therapy is not satisfactory, and more effective treatments are needed. In the search for new therapies for liver tumor, we found that Concanavalin A (Con A), a lectin from Jack bean seeds, can have a potent anti-hepatoma effect. Con A after binding to the mannose moiety on the cell membrane glycoprotein is internalized preferentially to the mitochondria. An autophagy is triggered which leads to cell death. Con A as a T cell mitogen subsequently activates the immune response in the liver and results in the eradication of the tumor in a murine in situ hepatoma model. The liver tumor nodule formation is inhibited by the CD8+ T cells, and a tumor antigen-specific immune memory is established during the hepatic inflammation. The dual properties (autophagic cytotoxicity and immunomodulation) via the specific carbohydrate binding let Con A exert a potent anti-hepatoma therapeutic effect. The novel mechanism of the Con A anti-hepatoma effect is discussed. The prototype of Con with an anti-hepatoma activity gives support to the search for other natural lectins as anti-cancer compounds.

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References
1.
Arbuthnot P, Kew M . Hepatitis B virus and hepatocellular carcinoma. Int J Exp Pathol. 2001; 82(2):77-100. PMC: 2517704. DOI: 10.1111/j.1365-2613.2001.iep0082-0077-x. View

2.
Kannagi R . Carbohydrate antigen sialyl Lewis a--its pathophysiological significance and induction mechanism in cancer progression. Chang Gung Med J. 2007; 30(3):189-209. View

3.
Trincheri N, Follo C, Nicotra G, Peracchio C, Castino R, Isidoro C . Resveratrol-induced apoptosis depends on the lipid kinase activity of Vps34 and on the formation of autophagolysosomes. Carcinogenesis. 2007; 29(2):381-9. DOI: 10.1093/carcin/bgm271. View

4.
Schumacher K, Schneider B, Reich G, Stiefel T, Stoll G, Bock P . Influence of postoperative complementary treatment with lectin-standardized mistletoe extract on breast cancer patients. A controlled epidemiological multicentric retrolective cohort study. Anticancer Res. 2004; 23(6D):5081-7. View

5.
Klionsky D, Abeliovich H, Agostinis P, Agrawal D, Aliev G, Askew D . Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes. Autophagy. 2008; 4(2):151-75. PMC: 2654259. DOI: 10.4161/auto.5338. View