Document Detail


The inducible effect of LBP on maturation of dendritic cells and the related immune signaling pathways in hepatocellular carcinoma (HCC).
MedLine Citation:
PMID:  22640039     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVE: To investigate the effect of LBP on differentiation and maturation of healthy human peripheral blood-derived dendritic cells cultured in different tumor microenvironment in vitro, and discuss the molecular and immunological mechanisms of LBP in treatment of tumor.
METHODS: In this study, we procured the peripheral blood-derived dendritic cells precursor cell by the Density gradient centrifugation method, and used the tumor-cell supernatant to prepare conditioned medium. The GM-CSF and IL-4 induced DCs precursor cell differentiation to DCs, the TNF-α promoted the immature DCs developed to mature DCs. In this way, we detected the influence of LBP on the expressions of surface molecules of DCs cultured in different environments, and especially on the role of related-immunity and NF-κB activity.
RESULTS: In LBP-treated group, the molecular phenotype of DCs, its capacity to stimulate allogeneic lymphocyte proliferation, and the levels of IL-12p70 and IFN-γ secretion were higher than the untreated group (p < 0.05), with statistical significance. Meanwhile the expression of NF-κB of the DCs in the medium treated by the LBP was higher than the untreated group (p < 0.05), also with statistical significance. Between the two different tumor microenvironment groups, the cell nucleus protein NF-κB expression is obviously different, the hepG2.2.15 group higher than the hepG2 group.
CONCLUSION: LBP could increase the expression of the phenotype of DCs, the secretion of IL-12p70 and IFN-γ in MLR, and enhance the NF-κB expression, especially in the virus-related group, suggesting LBP plays the anti-tumor role stronger in the virus-related environment and this phenomenon correlates with the NF-κB signaling pathway.
Authors:
Jing-Rui Chen; En-Qing Li; Cong-Qi Dai; Bin Yu; Xian-Lin Wu; Chun-Rong Huang; Xiao-Yin Chen
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Current drug delivery     Volume:  9     ISSN:  1875-5704     ISO Abbreviation:  Curr Drug Deliv     Publication Date:  2012 Jul 
Date Detail:
Created Date:  2012-07-05     Completed Date:  2012-11-02     Revised Date:  2014-07-31    
Medline Journal Info:
Nlm Unique ID:  101208455     Medline TA:  Curr Drug Deliv     Country:  United Arab Emirates    
Other Details:
Languages:  eng     Pagination:  414-20     Citation Subset:  IM    
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MeSH Terms
Descriptor/Qualifier:
Carcinoma, Hepatocellular / genetics,  immunology*,  metabolism
Cell Differentiation / drug effects,  genetics,  immunology
Cell Line, Tumor
Cell Proliferation / drug effects
Dendritic Cells / drug effects*,  immunology*,  metabolism
Drugs, Chinese Herbal / pharmacology*
Hep G2 Cells
Humans
Interferon-gamma / genetics,  immunology,  metabolism
Interleukin-12 / genetics,  immunology,  metabolism
Interleukin-4 / genetics,  immunology,  metabolism
Liver Neoplasms / genetics,  immunology*,  metabolism
Lymphocytes / drug effects,  immunology,  metabolism
NF-kappa B / genetics,  immunology,  metabolism
Signal Transduction / drug effects*,  genetics,  immunology
Tumor Microenvironment / drug effects,  genetics,  immunology
Tumor Necrosis Factor-alpha / genetics,  immunology,  metabolism
Chemical
Reg. No./Substance:
0/Drugs, Chinese Herbal; 0/NF-kappa B; 0/Tumor Necrosis Factor-alpha; 0/lycium barbarum polysaccharide; 187348-17-0/Interleukin-12; 207137-56-2/Interleukin-4; 82115-62-6/Interferon-gamma

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