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Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction
BACKGROUND: Ganoderma lucidum has been widely used as a herbal medicine for promoting health and longevity in China and other Asian countries. Polysaccharide extracts from Ganoderma lucidum have been reported to exhibit immuno-modulating and anti-tumor activities. In previous studies, F3, the active...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211495/ https://www.ncbi.nlm.nih.gov/pubmed/17996095 http://dx.doi.org/10.1186/1471-2164-8-411 |
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author | Cheng, Kun-Chieh Huang, Hsuan-Cheng Chen, Jenn-Han Hsu, Jia-Wei Cheng, Hsu-Chieh Ou, Chern-Han Yang, Wen-Bin Chen, Shui-Tein Wong, Chi-Huey Juan, Hsueh-Fen |
author_facet | Cheng, Kun-Chieh Huang, Hsuan-Cheng Chen, Jenn-Han Hsu, Jia-Wei Cheng, Hsu-Chieh Ou, Chern-Han Yang, Wen-Bin Chen, Shui-Tein Wong, Chi-Huey Juan, Hsueh-Fen |
author_sort | Cheng, Kun-Chieh |
collection | PubMed |
description | BACKGROUND: Ganoderma lucidum has been widely used as a herbal medicine for promoting health and longevity in China and other Asian countries. Polysaccharide extracts from Ganoderma lucidum have been reported to exhibit immuno-modulating and anti-tumor activities. In previous studies, F3, the active component of the polysaccharide extract, was found to activate various cytokines such as IL-1, IL-6, IL-12, and TNF-α. This gave rise to our investigation on how F3 stimulates immuno-modulating or anti-tumor effects in human leukemia THP-1 cells. RESULTS: Here, we integrated time-course DNA microarray analysis, quantitative PCR assays, and bioinformatics methods to study the F3-induced effects in THP-1 cells. Significantly disturbed pathways induced by F3 were identified with statistical analysis on microarray data. The apoptosis induction through the DR3 and DR4/5 death receptors was found to be one of the most significant pathways and play a key role in THP-1 cells after F3 treatment. Based on time-course gene expression measurements of the identified pathway, we reconstructed a plausible regulatory network of the involved genes using reverse-engineering computational approach. CONCLUSION: Our results showed that F3 may induce death receptor ligands to initiate signaling via receptor oligomerization, recruitment of specialized adaptor proteins and activation of caspase cascades. |
format | Text |
id | pubmed-2211495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22114952008-01-23 Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction Cheng, Kun-Chieh Huang, Hsuan-Cheng Chen, Jenn-Han Hsu, Jia-Wei Cheng, Hsu-Chieh Ou, Chern-Han Yang, Wen-Bin Chen, Shui-Tein Wong, Chi-Huey Juan, Hsueh-Fen BMC Genomics Research Article BACKGROUND: Ganoderma lucidum has been widely used as a herbal medicine for promoting health and longevity in China and other Asian countries. Polysaccharide extracts from Ganoderma lucidum have been reported to exhibit immuno-modulating and anti-tumor activities. In previous studies, F3, the active component of the polysaccharide extract, was found to activate various cytokines such as IL-1, IL-6, IL-12, and TNF-α. This gave rise to our investigation on how F3 stimulates immuno-modulating or anti-tumor effects in human leukemia THP-1 cells. RESULTS: Here, we integrated time-course DNA microarray analysis, quantitative PCR assays, and bioinformatics methods to study the F3-induced effects in THP-1 cells. Significantly disturbed pathways induced by F3 were identified with statistical analysis on microarray data. The apoptosis induction through the DR3 and DR4/5 death receptors was found to be one of the most significant pathways and play a key role in THP-1 cells after F3 treatment. Based on time-course gene expression measurements of the identified pathway, we reconstructed a plausible regulatory network of the involved genes using reverse-engineering computational approach. CONCLUSION: Our results showed that F3 may induce death receptor ligands to initiate signaling via receptor oligomerization, recruitment of specialized adaptor proteins and activation of caspase cascades. BioMed Central 2007-11-09 /pmc/articles/PMC2211495/ /pubmed/17996095 http://dx.doi.org/10.1186/1471-2164-8-411 Text en Copyright © 2007 Cheng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Cheng, Kun-Chieh Huang, Hsuan-Cheng Chen, Jenn-Han Hsu, Jia-Wei Cheng, Hsu-Chieh Ou, Chern-Han Yang, Wen-Bin Chen, Shui-Tein Wong, Chi-Huey Juan, Hsueh-Fen Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction |
title | Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction |
title_full | Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction |
title_fullStr | Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction |
title_full_unstemmed | Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction |
title_short | Ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction |
title_sort | ganoderma lucidum polysaccharides in human monocytic leukemia cells: from gene expression to network construction |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211495/ https://www.ncbi.nlm.nih.gov/pubmed/17996095 http://dx.doi.org/10.1186/1471-2164-8-411 |
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