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DOI 10.1186/1471-2164-8-411

Медицинская библиотека · BMC genomics · 2007

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

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Аннотация

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-alpha. 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.

Для цитирования: 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.. BMC genomics. 2007. DOI: 10.1186/1471-2164-8-411.

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