Document Detail

Plant lectins: Targeting programmed cell death pathways as antitumor agents.
MedLine Citation:
PMID:  21798364     Owner:  NLM     Status:  Publisher    
Lectins, a group of highly diverse, carbohydrate-binding proteins of non-immune origin that are ubiquitously distributed in plants, animals and fungi, are well-characterized to have numerous links a wide range of pathological processes, most notably cancer. In this review, we present a brief outline of the representative plant lectins including Ricin-B family, proteins with legume lectin domains and GNA family that can induce cancer cell death via targeting programmed cell death pathways. Amongst these above-mentioned lectins, we demonstrate that mistletoe lectins (MLs), Ricin, Concanavalin A (ConA) and Polygonatum cyrtonema lectin (PCL) can lead to cancer cell programmed death via targeting apoptotic pathways. In addition, we show that ConA and PCL can also result in cancer cell programmed death by targeting autophagic pathways. Moreover, we summarize the possible anti-cancer therapeutic implications of plant lectins such as ConA, Phaseolus vulgaris lectin (PHA) and MLs that have been utilized at different stages of preclinical and clinical trials. Together, these findings can provide a comprehensive perspective for further elucidating the roles of plant lectins that may target programmed cell death pathways in cancer pathogenesis and therapeutics. And, this research may, in turn, ultimately help cancer biologists and clinicians to exploit lectins as potential novel antitumor drugs in the future.
Lei-Lei Fu; Cheng-Cheng Zhou; Shun Yao; Jia-Ying Yu; Bo Liu; Jin-Ku Bao
Related Documents :
12676454 - Differentiating between local cytotoxicity, mitogenesis, and genotoxicity in carcinogen...
23264084 - Positive association of the vascular endothelial growth factor-a +405 gg genotype and p...
24862134 - Heparins and cancer survival: where do we stand?
23792484 - Pancreatic cancer: slow progression in the early stages.
8477404 - Development of an intervention to restore attention in cancer patients.
14646554 - Effects of bcl-2 overexpression on the sensitivity of mcf-7 breast cancer cells to rici...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-7-20
Journal Detail:
Title:  The international journal of biochemistry & cell biology     Volume:  -     ISSN:  1878-5875     ISO Abbreviation:  -     Publication Date:  2011 Jul 
Date Detail:
Created Date:  2011-7-29     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9508482     Medline TA:  Int J Biochem Cell Biol     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Copyright © 2011. Published by Elsevier Ltd.
School of Life Sciences & State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041, China.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Hypoxic alligator embryos: Chronic hypoxia, catecholamine levels and autonomic responses of in ovo a...
Next Document:  Comparative cytogenetics of opisthorchid species (Trematoda, Opisthorchiidae).